Patent Application
20220073901
This application contains a sequence listing in Computer Readable Form (CRF). The CFR file containing the sequence listing entitled “PJK4964444-SequenceListing.txt”, which was created on Nov. 19, 2021, and is 1,927 bytes in size. The information in the sequence listing is incorporated herein by reference in entirety.
The present invention relates to exosomes for elongating telomeres of cells, a composition containing the same, and a production method therefor, and more particularly, to exosomes for elongating telomeres of cells, which contain an RNA or protein of at least one gene selected from among TERT, TERF2, DKC1, TERF2IP, RFC1, RAD50, TERF1, PINX1, TNKS1BP1, ACD, NBN, HSPA1L, PARP1, PTGES3, SMG6, BLM, XRCC5, XRCC6, ERCC4, PRKDC, TEP1 and β-catenin, a composition containing the same, and a method of inducing telomere-elongating exosomes from cells by providing physical stimulation directly or indirectly to the cells.
Telomeres are DNA repeat structures (SEQ ID NO: 6, TTAGGG in humans) at both ends of chromosomes. Telomeres bind to the shelterin complex to form a protective cap, which regulates the multiplication ability of cells and prevents binding between chromosomes and loss of genetic information during cell division. Since DNA polymerase cannot completely amplify the 3′ end, telomeres are shortened by 30 to 200 bp for each cell division. When telomeres become shorter than the threshold value and become closer to the coding DNA and the loop structure of the telomeres cannot be maintained, the exposed telomeres are recognized by the p53 or p16INK4a signaling pathways, so that cell division stops and the cells die due to senescence.
Telomeres may be elongated by the reverse transcriptase telomerase, and the human telomerase complex is composed of TERC, which is an RNA molecule that acts as a template for telomere synthesis, TERT, which is a catalytic subunit, and telomerase-associated proteins such as DKC1 and TEP1. In normal cases, somatic cells have little telomerase activity, and high telomerase activity is detected only in stem cells and progenitor cells that require active division ability.
When the division of multiple cells is stopped as the telomeres are shortened, various problems may arise, and in particular, various symptoms represented by aging and degeneration may arise. It was already known that diseases that cause problems in the regeneration of bone marrow cells, such as congenital dyskeratosis congenita in which skin tissue is degenerated, and aplastic anemia in which blood cells counts are low, arise due to abnormalities in telomeres maintenance, such as mutations in telomerase or Shelterin complex-related genes containing the same. In recent years, studies have been reported that telomeres in patients suffering from aging-related diseases such as hypertension, metabolic syndrome, diabetes, and dementia are shorter than those in normal people, and thus studies on the possibility of slowing aging by increasing the length of telomeres have attracted attention. In addition, it has been shown that regenerative activities can be actively performed by increasing telomerase activity in somatic cells, which are generally known to have little telomerase activity. In particular, it has been reported that the increase in telomerase activity is effective when it is necessary to supplement various tissues such as the myocardium, liver, cornea, skin, blood vessels, cartilage and bone, immune cells, blood cells, etc. due to burns, injuries, aging and diseases. However, studies have also been reported that a number of cancer cells occurred in mice in which a gene capable of extending the length of telomeres was continuously overexpressed, suggesting that long telomeres become a risk factor for cancer. Therefore, it can be expected that, if telomeres can be temporarily elongated, this telomere elongation can alleviate various symptoms associated with aging and degeneration without the risk of cancer development, and can be particularly useful in the field of regenerative medicine.
According to the various utilities expected as described above, various methods for elongating telomeres have been developed. US Patent Application Publication No. 2018-0280413 discloses a pharmaceutical composition containing a compound for enhancing telomerase activity. However, in this case, a process of synthesizing the compound is required, and the composition obtainable through chemical synthesis requires that the starting material required for synthesis is purified. In addition, various by-products harmful to the environment are produced during the synthesis process, and the compound has a risk of producing by-products in in vivo metabolic processes. European Patent Publication No. 2959005 discloses an RNA encoding telomerase. In this case, synthesis and purification processes are also required, and since the RNA is hydrophilic, a delivery vehicle is additionally required to deliver the RNA into cells. Therefore, there is a need for a composition for telomere elongation that can be produced more simply, is less harmful, and has good efficiency.
The present invention has been made in order to solve the above-described problems, and exosomes according to one embodiment of the present invention contain an RNA or protein of at least one gene selected from among TERT, TERF2, DKC1, TERF2IP, RFC1, RAD50, TERF1, PINX1, TNKS1BP1, ACD, NBN, HSPA1L, PARP1, PTGES3, SMG6, BLM, XRCC5, XRCC6, ERCC4, PRKDC, TEP1 and β-catenin.
Another embodiment of the present invention provides a composition for elongating telomeres of cells, the composition containing the exosomes.
A method for producing exosomes for elongating telomeres of cells according to still another embodiment of the present invention comprises steps of: providing physical stimulation directly or indirectly to the cells; culturing a mixture of the cells and a medium for a predetermined time; and isolating exosomes from the mixture, wherein providing the stimulation directly to the cells comprises applying physical stimulation to the medium containing the cells, and providing the stimulation indirectly to the cells comprises applying physical stimulation to the medium not containing the cells and then mixing the medium and the cells.
Technical problems to be achieved by the present invention are not limited to the above-mentioned technical problem, and other technical problems which are not mentioned herein will be clearly understood by those skilled in the art from the following description.
As a technical means for achieving the above-described technical problem, exosomes for elongating telomeres of cells according to one aspect of the present invention contain an RNA or protein of at least one gene selected from among TERT, TERF2, DKC1, TERF2IP, RFC1, RAD50, TERF1, PINX1, TNKS1BP1, ACD, NBN, HSPA1L, PARP1, PTGES3, SMG6, BLM, XRCC5, XRCC6, ERCC4, PRKDC, TEP1 and β-catenin.
Here, the exosomes may be induced by providing physical stimulation to the cells.
The form of the physical stimulation may be any one selected from among ultrasound, heat, and light.
The physical stimulation may be provided directly or indirectly to the cells, wherein providing the stimulation directly to the cells comprises applying physical stimulation to the medium containing the cells, and providing the stimulation indirectly to the cells comprises applying physical stimulation to the medium not containing the cells and then mixing the medium and the cells.
A process of providing physical stimulation capable of inducing the exosomes may be performed by any one method selected from among: a method of mixing the cells and the medium and then providing physical stimulation to the mixture; or a method of providing physical stimulation to the medium and then mixing the medium and the cells; or a method of providing physical stimulation to the cells and then mixing the cells and the medium; or a method of providing physical stimulation to the cells and then mixing the cells and the medium, followed by providing physical stimulation to the mixture; or a method of providing physical stimulation to the medium and then mixing the medium and the cells, followed by providing physical stimulation to the mixture; or a method of providing physical stimulation to each of the cells and the medium and then mixing the cells and the medium; or a method of providing physical stimulation to each of the cells and the medium and then mixing the cells and the medium, followed by providing physical stimulation to the mixture.
The physical stimulation may be ultrasound stimulation, and providing the ultrasound stimulation directly to the cells may be performed at an ultrasound intensity of 0.1 to 3 W/cm2 and a frequency of 20 kHz to 20 MHz for a duration of 0.1 seconds to 20 minutes, and providing the ultrasound stimulation indirectly to the cells may be performed at an ultrasound intensity of 1 to 20 W/cm2 and a frequency of 20 kHz to 20 MHz for a duration of 0.1 seconds to 20 minutes.
The physical stimulation may be heat stimulation, and the heat stimulation may be applied by exposing the cells to a temperature of 40 to 50° C. for 1 to 10 minutes and then exposing the cells to a temperature of 0 to 4° C. for 5 to 10 seconds.
The physical stimulation may be light stimulation, and the light stimulation may be applied by irradiating a pulsed beam, which is selected from laser light or light-emitting diode light and has a wavelength of 300 to 900 nm, for 1 to 10 seconds.
The exosomes may contain 150 ng or more of total RNA in 1×108 exosome particles.
The exosomes may contain 1 μg or more of total RNA in 1×108 exosome particles.
When cells are treated with the exosomes, telomerase activity in the cells may increase.
When cells are treated with the exosomes, β-galactosidase activity in the cells may decrease.
A composition for elongating telomeres of cells according to another aspect of the present invention contains the above-described exosomes.
Here, the composition may contain the exosomes at a concentration of 106 to 1014 exosomes/ml.
A method for producing exosomes for elongating telomeres of cells according to still another embodiment of the present invention comprises steps of: providing physical stimulation directly or indirectly to the cells; culturing a mixture of the cells and a medium for a predetermined time; and isolating exosomes from the mixture, wherein providing the stimulation directly to the cells comprises applying physical stimulation to the medium containing the cells, and providing the stimulation indirectly to the cells comprises applying physical stimulation to the medium not containing the cells and then mixing the medium and the cells.
Here, the form of the physical stimulation may be any one selected from among ultrasound, heat, and light.
The step of providing the physical stimulation directly or indirectly to the cells may be performed by any one method selected from among: a method of mixing the cells and the medium and then providing physical stimulation to the mixture; or a method of providing physical stimulation to the medium and then mixing the medium and the cells; or a method of providing physical stimulation to the cells and then mixing the cells and the medium; or a method of providing physical stimulation to the cells and then mixing the cells and the medium, followed by providing physical stimulation to the mixture; or a method of providing physical stimulation to the medium and then mixing the medium and the cells, followed by providing physical stimulation to the mixture; or a method of providing physical stimulation to each of the cells and the medium and then mixing the cells and the medium; or a method of providing physical stimulation to each of the cells and the medium and then mixing the cells and the medium, followed by providing physical stimulation to the mixture.
The physical stimulation may be ultrasound stimulation, and providing the ultrasound stimulation directly to the cells may be performed at an ultrasound intensity of 0.1 to 3 W/cm2 and a frequency of 20 kHz to 20 MHz for a duration of 0.1 seconds to 20 minutes, and providing the ultrasound stimulation indirectly to the cells may be performed at an ultrasound intensity of 1 to 20 W/cm2 and a frequency of 20 kHz to 20 MHz for a duration of 0.1 seconds to 20 minutes.
The physical stimulation may be heat stimulation, and the heat stimulation may be applied by exposing the cells to a temperature of 40 to 50° C. for 1 to 10 minutes and then exposing the cells to a temperature of 0 to 4° C. for 5 to 10 seconds.
The physical stimulation may be light stimulation, and the light stimulation may be applied by irradiating a pulsed beam, which is selected from laser light or light-emitting diode light and has a wavelength of 300 to 900 nm, for 1 to 10 seconds.
The cells may be selected from the group consisting of mammalian stem cells, progenitor cells, fibroblasts, keratinocytes or organ tissue cells.
The medium may be selected from a culture medium or a differentiation-inducing medium.
The culturing of the mixture may be performed for 1 hour to 10 days.
The step of isolating the exosomes may be performed using one or more of ultracentrifugation, density gradient separation, filtration, size exclusion chromatography, immunoaffinity separation, precipitation, and microfluidic separation.
The step of isolating the exosomes may comprise steps of: centrifuging the mixture after the culturing to obtain a supernatant; filtering the supernatant through a filter to obtain a filtrate; and concentrating the filtrate.
The expression level of one or more of TERT, TERF2, DKC1, TERF2IP, RFC1, RAD50, TERF1, PINX1, TNKS1BP1, ACD, NBN, HSPA1L, PARP1, PTGES3, SMG6, BLM, XRCC5, XRCC6, ERCC4, PRKDC, TEP1 and β-catenin genes in the isolated exosomes may be higher than that in exosomes secreted from the cells before being subjected to the production method.
When cells are treated with the isolated exosomes, telomerase activity in the cells may increase.
When cells are treated with the isolated exosomes, β-galactosidase activity in the cells may decrease.
When cells are treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, migration of the cells may increase.
When tissue is treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, regeneration of the tissue may be promoted.
When a wound is treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, healing of the wound may be promoted.
When a scar is treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, healing of the scar may be promoted.
When cells are treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, the exosomes may have an anti-senescence effect on the cells.
The above-described means for solving the problem is merely exemplary and should not be construed as limiting the present invention. In addition to the above-described exemplary embodiments, additional embodiments may exist in the drawings and the detailed description of the invention.
The composition for elongating telomeres of cells according to one embodiment of the present invention is simpler to produce than the above-described conventional composition for elongating telomeres. That is, the compound in the conventional composition is chemically synthesized, and this chemical synthesis has no specificity and requires a long and complex process. In contrast, the method for elongating telomeres of cells according to one embodiment of the present invention may promote the expression of various factors associated with telomere elongation and the production of exosomes containing the factors even by a simple process of treating the cells with physical stimulation, and is composed of a process of isolating the secreted exosomes from the conditioned medium of the cells, and thus the process thereof is simple. In addition, since cells are surrounded by a double lipid membrane, the intracellular endocytosis of hydrophilic nucleic acid, which is required for the nucleic acid exhibits an effect, is difficult without a delivery vehicle capable of delivering the nucleic acid into cells, and thus a step of loading the nucleic acid into the delivery vehicle is additionally required. However, according to the method for producing exosomes according to the present invention, telomere elongation-related factors are obtained in a form surrounded by a lipid membrane, there is no need to perform additional loading.
In addition, the composition for elongating telomeres of cells according to one embodiment of the present invention is superior in terms of efficiency and application method compared to the previously disclosed composition. That is, the above-described compound for increasing telomerase activity needs to be injected into the body at a high concentration so that it exhibits a sufficient effect, whereas the exosomes for elongating telomeres of cells according to one embodiment of the present invention may exhibit an effect by applying a small amount of the exosomes by a non-invasive method such as topical application.
In addition, since the method for producing exosomes for elongating telomeres of cells according to one embodiment of the present invention induces secretion of a large amount of exosomes containing large amounts of telomere elongation-related factors, it is advantageous in terms of the high-yield production of exosomes containing useful substances from cells.
In addition, the exosomes for elongating telomeres of cells according to one embodiment of the present invention has high safety. That is, the compound may pose additional risks such as toxicity in the metabolic process, and particularly, in the above-described conventional technology, the dosage of the compound is quite high (the order of mg per kg weight of a subject animal, and waste that burden the environment is also generated in the synthesis process. However, this burden is relatively small in the method according to the present invention.
In addition, it was confirmed that the exosomes for elongating telomeres of cells according to one embodiment of the present invention induce cell division and have anti-aging and tissue regeneration effects, in addition to elongating telomeres. Thereby, it is expected that the exosomes of the present invention can ameliorate and prevent not only problems caused by shortening of telomeres, but also various diseases and conditions associated with aging and tissue regeneration.
It is to be understood that the effects of the present invention are not limited to the above-described effects, and include all effects that may be deduced from the features described in the detailed description of the invention or the claims.
Hereinafter, the present invention will be described in more detail. However, the present invention may be embodied in various different forms and is not limited by the embodiments described herein, and the scope of the present invention should be defined only by the appended claims.
The terminology used herein is only for the purpose of describing particular embodiments and is not intended to be limiting of the present invention. Singular expressions include plural expressions unless otherwise specified in the context thereof. Throughout the present specification, it is to be understood that when any part is referred to as “comprising” any component, it does not exclude other components, but may further comprise other components, unless otherwise specified.
In addition, the unique name of each gene used under the designation “gene” in the present invention is an officially known gene name, a commonly used name, or the name of a product of the gene, for example, a protein in the case of the gene encoding the protein.
The present inventors previously disclosed in Korean Patent No. 10-1855967 that, when physical stimulation capable of promoting environmental inflow is provided to a mixture of cells and a culture medium and the mixture is provided with the physical stimulation is cultured for a predetermined time, the cells can be reprogrammed, and when cells are treated with exosomes isolated from the mixture, reprogramed cells may be obtained. Here, the direction of reprogramming appears differently depending on the composition of the medium upon application of physical stimulation regardless of the type of cells provided with physical stimulation or the type of cells treated with the exosomes. In a subsequent process of analyzing the effect of the cell reprogramming method, it was confirmed that the expression of the gene group related to telomere elongation was also increased by applying physical stimulation. Through further research thereon, it has been found that, unlike the previously disclosed invention described above, telomeres can be elongated by physical stimulation regardless of not only the type of cells tested but also the composition of medium. Based on this finding, it was possible to conclude that telomere elongation was elongated by the physical stimulation itself rather than the environmental inflow. At this time, it was found that expression of telomere elongation-related factors increased, and secretion of exosomes containing these factors also significantly increased. Based on this finding, a new invention is disclosed.
Exosomes according to one aspect of the present invention contain an RNA or protein of at least one gene selected from among TERT, TERF2, DKC1, TERF2IP, RFC1, RAD50, TERF1, PINX1, TNKS1BP1, ACD, NBN, HSPA1L, PARP1, PTGES3, SMG6, BLM, XRCC5, XRCC6, ERCC4, PRKDC, TEP1 and β-catenin. Most preferably, the exosomes may contain the RNAs or proteins of all the above-described genes.
Here, TERT (telomerase reverse transcriptase) is a subunit having telomerase catalytic activity, and TERF1 (telomeric repeat binding factor 1) and TERF2 (telomeric repeat binding factor 2) recognize the telomere sequence. It is known that DKC1 (dyskerin pseudouridine synthase 1), RFC1 (replication factor C subunit 1), TNKS1BP1 (tankyrase 1 binding protein 1), NBN (Nibrin), HSPA1L (heat shock protein family A member 1 like), PARP1 (poly ADP-ribose polymerase 1), PTGES3 (prostaglandin E synthase 3), SMG6 (Smg6 homolog, Nonsense mediated mRNA decay factor), XRCC5 (X-ray repair cross complementing 5) and XRCC6 (X-ray repair cross complementing 6) are necessary for stabilization and maintenance of telomeres. It has been reported that TERF2IP (TERF2 interacting protein) and RAD50 (RAD50 homolog, double strand break repair protein) inhibit telomere recombination, and PINX1 (PIN2/TERF1-interacting telomerase inhibitor 1) mediate the accumulation of TERF1 and TERT in the nucleolus, help TRF1 bind to telomerase, and inhibit telomerase activity in the S phase. ACD (adrenocortical dysplasia protein homolog), ERCC4 (excision repair cross-complementation group 4) and PRKDC (protein kinase, DNA-activated, catalytic subunit) are necessary to control the telomere length and for telomere protection, and promote telomere amplification during BLM (bloom syndrome protein) DNA synthesis, and telomerase associated protein 1 (TEP1) forms part of the telomerase complex. β-Catenin is a transcriptional regulator that promotes TERT expression. It has been reported that the above-described factors all have effects on the elongation and stabilization of telomeres. The exosomes for elongating telomeres, which contain the above-described gene products, may be used for various effects as described below.
The exosomes may be induced by providing physical stimulation to cells.
The form of the physical stimulation may be selected from among low frequency, ultrasound, high frequency, heat, light, electric wave, radio wave, stretch, and compression, and may preferably be any one selected from among ultrasound, heat, and light.
The physical stimulation may be provided directly or indirectly to the cells, wherein providing the stimulation directly to the cells may comprise applying physical stimulation to the medium containing the cells, and providing the stimulation indirectly to the cells may comprise applying physical stimulation to the medium not containing the cells and then mixing the medium and the cells.
A process of providing physical stimulation capable of inducing the exosomes may be performed by any one method selected from among: a method of mixing the cells and the medium and then providing physical stimulation to the mixture; or a method of providing physical stimulation to the medium and then mixing the medium and the cells; or a method of providing physical stimulation to the cells and then mixing the cells and the medium; or a method of providing physical stimulation to the cells and then mixing the cells and the medium, followed by providing physical stimulation to the mixture; or a method of providing physical stimulation to the medium and then mixing the medium and the cells, followed by providing physical stimulation to the mixture; or a method of providing physical stimulation to each of the cells and the medium and then mixing the cells and the medium; or a method of providing physical stimulation to each of the cells and the medium and then mixing the cells and the medium, followed by providing physical stimulation to the mixture. The physical stimulation may be provided directly or indirectly to the cells one or more times or provided using a combination of one or more selected from the above methods, and as the number of times increases, the telomere elongation effect of the exosomes may increase proportionally. When the physical stimulation is provided one or more times as described above, it is preferable to provide a time interval between the provisions so that the cells can recover, and the time interval may be at least 1 day, more preferably at least 2 days.
The physical stimulation may be ultrasound stimulation. Providing the ultrasound stimulation directly to the cells may be performed at an ultrasound intensity of 0.1 to 3 W/cm2 and a frequency of 20 kHz to 20 MHz for a duration of 0.1 seconds to 20 minutes, and providing the ultrasound stimulation indirectly to the cells may be performed at an ultrasound intensity of 1 to 20 W/cm2 and a frequency of 20 kHz to 20 MHz for a duration of 0.1 seconds to 20 minutes. More preferably, providing the ultrasound stimulation directly to the cells may be performed at an ultrasound intensity of 0.5 to 2 W/cm2 and a frequency of 20 kHz to 2 MHz for a duration of 0.1 seconds to 10 minutes, and providing the ultrasound stimulation indirectly to the cells may be performed at an ultrasound intensity of 2 to 10 W/cm2 and a frequency of 20 kHz to 2 MHz for a duration of 1 second to 15 minutes.
The physical stimulation may be heat stimulation, and the heat stimulation may be applied by exposing the cells to a temperature of 40 to 50° C. for 1 to 10 minutes and then exposing the cells to a temperature of 0 to 4° C. for 5 to 10 seconds.
The physical stimulation may be light stimulation, and the light stimulation may be applied by irradiating a pulsed beam, which is selected from laser light or light-emitting diode light and has a wavelength of 300 to 900 nm, for 1 to 10 seconds.
The exosomes may contain at least 100 ng, preferably at least 150 ng, more preferably at least 150 ng, of total RNA in 1×108 exosome particles.
The exosomes may contain at least 0.5 μg, preferably at least 1 μg, more preferably at least 1.2 g, of total RNA in 1×108 exosome particles.
When cells are treated with the exosomes, telomerase activity in the cells may increase. This increase in telomerase activity may lead to elongation of telomere length and promotion of cell division after cell treatment with the exosomes.
When cells are treated with the exosomes, β-galactosidase activity in the cells may decrease. (3-galactosidase is an enzyme that catalyzes the hydrolysis of β-galactoside into monosaccharides, and the lysosomal β-galactosidase is overexpressed and accumulated in senescent cells. As a result, it has been reported that the activity of β-galactosidase in senescent cells is high. It was confirmed that, when cells were treated with the exosomes for elongating telomeres of cells according to one embodiment of the present invention, the activity of the enzyme decreased, suggesting that the exosomes have an anti-aging effect.
A composition for elongating telomeres of cells according to another aspect of the present invention contains the above-described exosomes.
The exosomes contain gene products of various factors functioning to elongate and stabilize telomeres. The exosomes migrate along the bloodstream and exhibit therapeutic effects by delivering the factors directly to cells. Thus, a composition containing these exosomes may be used for therapeutic purposes in a subject in need of the activities of these genes. For example, the composition may be used for the treatment or amelioration of diseases known to occur due to abnormal telomere maintenance, such as congenital dysphagia, aplastic anemia, Werner syndrome, Bloom syndrome, Ataxia-telangiectasia, Nijmegen breakage syndrome, Ataxia-telangiectasia-like syndrome, and pulmonary fibrosis. In addition, the composition may be used for the treatment or amelioration of various diseases and conditions caused by cell senescence and loss, for example, various degenerative diseases such as dementia, ataxia, and degeneration of cartilage and bone, autoimmune diseases such as Crohn's disease and chronic obstructive pulmonary disease, hypertension, metabolic syndrome, diabetes, skin aging, pigmentation abnormalities, hair loss, skin aging, etc. In addition, the composition may be used for rapid regeneration from various injuries such as burns, wounds, injuries, organ failure, organ loss, and ulcers.
Here, the composition may contain the exosomes at a concentration of at least 102 exosomes/ml, preferably 106 to 1014 exosomes/ml.
The composition may be administered by any one method selected from oral, intravenous, intramuscular, subcutaneous, intradural, and transdermal administration. Preferably, the composition may be administered subcutaneously or transdermally. The composition may contain a pharmaceutically acceptable diluent, preservative, solubilizing agent, emulsifier, adjuvant, buffer and carrier, in addition to an effective amount of the above-described exosomes. Ingredients that may be contained in the composition include buffers such as neutral buffered saline and phosphate buffered saline, carbohydrates such as glucose, mannose, sucrose, dextran and mannitol, amino acids such as polypeptides and glycine, antioxidants, EDTA, chelating reagents such as glutathione, adjuvants such as aluminum hydroxide, and preservatives.
Since the selection of the administration route and the additional ingredients and compositions according to each administration route are known to those skilled in the art, detailed descriptions thereof will be omitted.
A method for producing exosomes for elongating telomeres of cells according to still another embodiment of the present invention comprises steps of: providing physical stimulation directly or indirectly to the cells; culturing a mixture of the cells and a medium for a predetermined time; and isolating exosomes from the mixture, wherein providing the stimulation directly to the cells comprises applying physical stimulation to the medium containing the cells, and providing the stimulation indirectly to the cells comprises applying physical stimulation to the medium not containing the cells and then mixing the medium and the cells.
Here, the form of the physical stimulation may be selected from among low frequency, ultrasound, high frequency, heat, light, electric wave, radio wave, stretch, and compression, and may preferably be any one selected from among ultrasound, heat, and light.
The step of providing physical stimulation directly or indirectly to the cells may be performed by any one method selected from among: a method of mixing the cells and the medium and then providing physical stimulation to the mixture; or a method of providing physical stimulation to the medium and then mixing the medium and the cells; or a method of providing physical stimulation to the cells and then mixing the cells and the medium; or a method of providing physical stimulation to the cells and then mixing the cells and the medium, followed by providing physical stimulation to the mixture; or a method of providing physical stimulation to the medium and then mixing the medium and the cells, followed by providing physical stimulation to the mixture; or a method of providing physical stimulation to each of the cells and the medium and then mixing the cells and the medium; or a method of providing physical stimulation to each of the cells and the medium and then mixing the cells and the medium, followed by providing physical stimulation to the mixture. The physical stimulation may be provided directly or indirectly to the cells one or more times or provided using a combination of one or more selected from the above methods, and as the number of times increases, the telomere elongation effect of the exosomes may increase proportionally. When the physical stimulation is provided one or more times as described above, it is preferable to provide a time interval between the provisions so that the cells can recover, and the time interval may be at least 1 day, more preferably at least 2 days.
The physical stimulation may be ultrasound stimulation. Providing the ultrasound stimulation directly to the cells may be performed at an ultrasound intensity of 0.1 to 3 W/cm2 and a frequency of 20 kHz to 20 MHz for a duration of 0.1 seconds to 20 minutes, and providing the ultrasound stimulation indirectly to the cells may be performed at an ultrasound intensity of 1 to 20 W/cm2 and a frequency of 20 kHz to 20 MHz for a duration of 0.1 seconds to 20 minutes. More preferably, providing the ultrasound stimulation directly to the cells may be performed at an ultrasound intensity of 0.5 to 2 W/cm2 and a frequency of 20 kHz to 2 MHz for a duration of 0.1 seconds to 10 minutes, and providing the ultrasound stimulation indirectly to the cells may be performed at an ultrasound intensity of 2 to 10 W/cm2 and a frequency of 20 kHz to 2 MHz for a duration of 1 second to 15 minutes.
The physical stimulation may be heat stimulation, and the heat stimulation may be applied by exposing the cells to a temperature of 40 to 50° C. for 1 to 10 minutes and then exposing the cells to a temperature of 0 to 4° C. for 5 to 10 seconds.
The physical stimulation may be light stimulation, and the light stimulation may be applied by irradiating a pulsed beam, which is selected from laser light or light-emitting diode light and has a wavelength of 300 to 900 nm, for 1 to 10 seconds, more preferably 3 to 7 seconds.
It was confirmed that, when the method for producing exosomes for elongating telomeres of cells according to one embodiment of the present invention was applied to various types of cells, it induced secretion of exosomes capable of elongating telomeres from all the types of cells. The cells may be selected from the group consisting of mammalian stem cells, progenitor cells, fibroblasts, keratinocytes, or organ tissue cells. When the cells having elongated telomeres are used for in vivo application, the cells may be either autologous, allogeneic or heterologous. When the cells are heterologous, the cells may be of mammalian origin. In order to reduce the likelihood of immune rejection, the cells are preferably allogeneic cells, most preferably autologous cells. The cells may be selected from the group consisting of mammalian stem cells, progenitor cells, fibroblasts, keratinocytes, or organ tissue cells.
The medium may be selected from a culture medium or a differentiation-inducing medium. Here, the term “culture medium” refers to a medium optimized for survival of a specific type of cells while maintaining the uniformity of the cells, which is a medium that is used for uniform cell proliferation. On the other hand, the term “differentiation inducing medium” refers to a medium for inducing differentiation of a specific type of cells into another type of cells having other differentiation potentials or functions.
The culturing of the mixture may be performed for 1 hour to 10 days, preferably 1 to 5 days. The reason therefor is as follows. The reason why this culture time is necessary is as follows. When the above-described physical stimulation is applied to cells, the expression of various genes described later is increased, and in this case, “gene expression” involves transcription, the synthesis and folding of a bioactive substance such as a protein, and the migration of the substance to a necessary position in the cell, and hence it takes time to actually produce exosomes loaded with a bioactive substance having a telomere elongation effect. In addition, it was found that the production of exosomes decreases over time after ultrasound treatment, indicating that an excessively long culture time may not be helpful in the efficiency of exosome production.
The step of isolating the exosomes may be performed using one or more of ultracentrifugation, density gradient separation, filtration, size exclusion chromatography, immunoaffinity separation, precipitation, and microfluidic separation.
The step of isolating the exosomes may comprise steps of: centrifuging the mixture after the culturing to obtain a supernatant; filtering the supernatant through a filter to obtain a filtrate; and concentrating the filtrate.
The expression level of one or more of TERT, TERF2, DKC1, TERF2IP, RFC1, RAD50, TERF1, PINX1, TNKS1BP1, ACD, NBN, HSPA1L, PARP1, PTGES3, SMG6, BLM, XRCC5, XRCC6, ERCC4, PRKDC, TEP1 and β-catenin genes in the isolated exosomes may be higher than that in exosomes secreted from the cells before being subjected to the production method. These genes are known to have functions such as telomere elongation, stabilization and protection, and it was confirmed that, when cells were treated with the exosomes produced by the above-described method, the exosomes promoted telomere elongation and cell growth and also had an anti-aging effect.
When cells are treated with the exosomes, telomerase activity in the cells may increase. This increase in telomerase activity may lead to elongation of telomere length and promotion of cell division after cell treatment with the exosomes.
When cells are treated with the exosomes, β-galactosidase activity in the cells may decrease. As described above, the enzyme β-galactosidase is overexpressed in senescent cells and accumulated in lysosomes, and thus exhibits high activity. It was confirmed that, when cells were treated with exosomes produced by the production method according to one embodiment of the present invention, the activity of the enzyme decreased.
When cells are treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, migration of the cells may increase.
When tissue is treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, regeneration of the tissue may be promoted. As will be described later, the exosomes may increase cell migration and cell proliferation, and may increase expression of a number of genes associated with cell cycle, proliferation and metabolism, in addition to telomere-related genes. This regeneration may target not only physical damage but also chemical damage.
When a wound is treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, healing of the wound may be promoted.
When a scar is treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, healing of the scar may be promoted.
When cells are treated with the isolated exosomes obtained in the method for producing exosomes for elongating telomeres of cells, the exosomes may have an anti-senescence effect on the cells. As described above, it was confirmed that, when cells were treated with exosomes produced by the production method according to one embodiment, β-galactosidase activity in the cells could decrease, and migration and proliferation of the cells could also increase. These effects appears not only in normal cells, but also in progeria patient's cells having problems in terms of telomere elongation, and the above-described exosomes may be used to delay and prevent senescence or to treat accelerated aging such as progeria.
Hereinafter, examples of the present invention will be described in detail so that the present invention can be easily carried out by those skilled in the art. However, the present invention may be embodied in various different forms, and is not limited to the examples described herein.
All cell culture processes in the Examples and Experimental Examples of the present invention were performed at 37° C. under 5% CO2.
Ultrasound stimulation was applied to 1×106 cells in 1 ml of medium at an ultrasound intensity of 1 W/cm2 and a frequency of 20 KHz for 5 seconds, and the cells were cultured with the same medium in a culture dish for 1 day or more.
1×106 cells in 1 ml of hES medium were placed in a 1.5-ml tube and exposed to 50° C. for 5 seconds and then exposed to 0° C. for 10 seconds, and the cells were cultured with the same medium in a culture dish for 1 day or more.
Light-emitting diode light stimulation (1 W, 500 Hz/sec) with a wavelength of 808 nm was applied directly to 1×106 cells in 1 ml of hES medium for 5 seconds, and the cells were cultured with the same medium in a culture dish for 1 day or more.
hES medium was treated with ultrasound at 0, 3, 5 and 10 W/cm2 for 10 minutes and then mixed with non-ultrasound-treated cells, followed by 1 day or more of culture.
Ultrasound stimulation was applied to 1×106 cells in 1 ml of medium at an ultrasound intensity of 1 W/cm2 and a frequency of 20 KHz for 5 seconds, and the cells were cultured with the same medium in a culture dish for 1 to 2 days. Next, the conditioned medium was collected and centrifuged at 3000 rpm for 5 minutes to remove cell debris or dead cells, and only the supernatant was collected and filtered through a 0.2-μm filter. The filtrate containing only components having a size of 0.2 m or less was collected, placed in a 100-kDa filter, and centrifuged at 10,000×g for 30 minutes to remove components having a molecular weight of 100 kDa or less, thus obtaining concentrated exosomes. PBS was added to the 100-kDa filter containing the concentrated exosomes and washed at 10000×g for 5 minutes, and this addition and washing process was repeated twice to remove the medium component from the exosome concentrate, thus obtaining exosomes.
The exosomes (reprosome) produced according to Example 5 were added to medium at a concentration of 1×109 particles/ml, and cells were cultured in the medium.
In order to compare the effect of Example 1 depending on the type of cells, ultrasound stimulation was added to each of the following types of 1×106 cells in 1 ml of DMEM medium (fibroblast culture medium) according to the method of Example 1: CB-HDFs (CellBio), Adipo-MSC cells (professor Hwang Dong-Yeon Lab.), HDFa cells (Invitrogen), HFF cells (Cha University), Hef cells (Cha University), GFP-HDF cells (GFP-HNDFs, Angio-proteomie), skin fibroblasts (obtained from a 60-year-old stroke patient sample in compliance with the IRB-approved protocol), HDP cells (CellBio), L132 cells (ATCC), h-PreAdipo cells (ATCC), CB-HDF x/Entr cells, and MSC x/Entr cells (here, CB-HDF x/Entr and MSC x/Entr cells are pluripotent cells derived from CB-HDF and MSC cells, respectively, in human embryonic stem cell culture medium by application of a method of inducing pluripotent cells through ultrasound treatment in the study conducted by the present inventor (Lee et al., An ultra-effective method of generating extramultipotent cells from human fibroblasts by ultrasound, Biomaterials, 2017.)). Then, the cells were cultured for 0, 1 and 2 days, and the telomere lengths in the cells were analyzed according to a qPCR method using a kit (Absolute Human Telomere Length Quantification qPCR Assay Kit, Cat No. 8918, ScienCell™). As a result, as shown in
To analyze the effect of physical stimulation on telomere analysis depending on the kind of physical stimulation, each physical stimulation was added to CB-HDFs in human embryonic stem cell culture medium according to the methods of Examples 1 to 3, and then the cells were cultured for 0, 1 and 2 days, and the telomere length in the cells was analyzed according to a qPCR method. As a result, as shown in
In order to examine whether telomeres are elongated even by indirect physical stimulation, not by direct physical stimulation, indirect ultrasound stimulation was applied to CB-HDFs according to the method of Example 2, and then the cells were cultured for 1 day, and the telomere length in the cells were analyzed according to a qPCR method. As a result, as shown in
In order to compare the effect of Example 1 depending on the composition of medium, ultrasound was applied to 1×106 CB-HDFs in 1 ml of each of human embryonic stem cell culture medium, neural stem cell culture medium, primary germ cell culture medium and DMEM medium according to the method of Example 1, and then the cells were cultured for 0, 1 and 2 days, and the telomere length in the cells was analyzed according to a qPCR method. As a result, as shown in
In order to examine whether a difference appears when the ultrasound according to Example 1 is repeated, ultrasound stimulation was applied to 1×106 CB-HDFs in 1 ml of DMEM medium according to the method of Example 1, and the cells were cultured for 1, 3 and 6 days. In this case, the ultrasound stimulation was applied one time or applied every 2 days. The telomere length in the cells was analyzed according to a qPCR method. As a result, as shown in
In order to examine whether the method of Example 1 shows a difference in the expression level of TERT gene depending on the type of cells, ultrasound stimulation was applied to each of the following types of 1×106 cells according to the method of Example 1: CB-HDFs, Adipo-MSC cells, HDF cells, HFF cells, Hef cells, GFP-HDF cells, skin fibroblasts, HDP cells, L132 cells, h-PreAdipo cells, CB-HDF x/Entr cells and MSC x/Entr cells. Then, the cells were cultured for 0, 1 and 2 days, and changes in TERT gene expression in the cells were analyzed according to a qPCR method. As a result, as shown in
In order to examine how the telomere elongation method according to Example 1 affects the (3-catenin gene which is a transcriptional activator of TERT, ultrasound stimulation was applied to 1×106 CB-HDFs in 1 ml of DMEM medium and 1×106 Adipo-MSC cells in 1 ml of DMEM medium according to the method of Example 1, and then the cells were cultured for 0, 1 and 2 days, and changes in β-catenin gene expression in the cells were analyzed according to a qPCR method. As a result, as shown in
In order to examine how the telomere elongation method according to Example 1 affects telomerase activity, ultrasound stimulation was applied to 1×106 CB-HDFs in 1 ml of DMEM medium and 1×106 Adipo-MSC cells in 1 ml of DMEM medium according to the method of Example 1, and then the cells were cultured for 0, 1 and 2 days, and telomerase activities in the cells were analyzed by Sciencell's Telomerase Activity Quantification qPCR kit (TAQ). As a result, as shown in
In order to further confirm that telomere elongation is induced by the telomere elongation method according to Example 1, ultrasound stimulation was applied to 1×106 CB-HDFs in 1 ml of DMEM medium and 1×106 Adipo-MSC cells in 1 ml of DMEM medium according to the method of Example 1, and then the cells were cultured for 1 day. Then, fluorescence in situ hybridization (FISH) analysis was performed using a TelG telomere probe (SEQ ID NO: 11, TTAGGGTTAGGGTTAGGG), and fluorescent signals were analyzed with a confocal microscope. At this time, the cells were counterstained with Hoechst 33342. As a result, as shown in
In order to confirm whether TERT gene expression induced by the telomere extension method according to Example 1 leads to an increase in protein expression, ultrasound stimulation was applied to 1×106 CB-HDFs in 1 ml of DMEM medium according to the method of Example 1, and the cells were cultured for 1 day, and then fluorescence-stained using anti-Ki67 and anti-TERT antibodies and observed with a confocal microscope. As a result, as shown in
In order to examine how the above-described changes caused by the telomere elongation method according to Example 1 affects cell senescence, ultrasound stimulation was applied to 1×106 CB-HDFs in 1 ml of DMEM medium according to the method of Example 1, and the cells were cultured for 1 day and 3 days. Then, a test for β-galactosidase activity known to have a correlation with intracellular senescence was performed using X-gal, followed by analysis with a phase contrast microscope. At this time, the ultrasound treatment was performed one time or performed every 2 days. As a result, as shown in
Exosomes were produced according to the method of Example 5, and the exosome production efficiency was analyzed. First, expression of an exosome marker (CD63) in HDFs 24 hours after ultrasound treatment was analyzed immunofluorescence staining (at this time, counter staining was performed using the nuclear staining dye DAPI). As a result, it could be confirmed that the expression of the exosome marker significantly increased in the exosome-treated cells compared to the non-exosome-treated group (
Next, analysis was performed as to whether there were changes in the total amounts of RNA and protein in the exosomes whose secretion was induced by ultrasound treatment as described in Example 5. Total RNA was extracted from the exosomes using TRIzol (RNAi, Takara, Otsu, Japan), and then quantified by Agilent 2100 Bioanalyzer (Agilent, Santa Clara, Calif., USA). As a result, it could be confirmed that the amount of total RNA in the exosomes secreted from 1×106 cells was 1003.5±167.6 ng when ultrasound treatment performed was performed as described in Example 5, which was at least 5 times larger than when ultrasound treatment was not performed (186.3±17.3 ng). At this time, the amount of total RNA in the same number of exosomes (1×108 exosomes) was 222.4±37.1 ng in the case of ultrasound treatment, which was similar to that in the case of non-ultrasound treatment (241.5±22.5 ng) (
In order to identify RNAs in the exosomes produced according to Example 5, RNA-seq was performed and gene ontology analysis was performed. As a result, it was confirmed that a number of genes associated with telomere maintenance and protection, cell cycle and proliferation, and DNA repair and amplification were present in the exosomes (
In addition, as a result of RNAs associated with cell proliferation, telomere lengthening and anti-senescence in the exosomes by qPCR, it could be confirmed that RNAs of cell proliferation-related cyclin-D1 and PCNA, telomere lengthening-related Ctnnb1, TERT and STAT3, and anti-senescence-related TEP1, MMP1, MMP2, MMP9, elastin, keratin, HYAL1, laminin, filaggrin and invducrin, significantly increased compared to those in the control group in which they were hardly detected (
To confirm TERT protein in the exosomes secreted by ultrasound stimulation, immunofluorescence staining for the exosome marker and the TERT protein was performed. As a result, it was possible to confirm a number of portions where the two signals overlap (
In order to examine how the exosomes produced according to Example 5 affect telomere elongation in cells, the cells were cultured in a culture medium containing the exosomes, and after 2 days, the telomere length was analyzed according to a qPCR method. As a result, it was confirmed that, as the concentrations of the exosomes increased, the telomere length significantly increased in the exosome-treated cells compared to the cells (con) before exosome treatment and the group (non) cultured for 2 days without exosome treatment (
Next, in order to examine whether the telomeres elongation effect of the exosome appears differently depending on the type of cells, each type of HDF, HEK, HDP and Adipo-MSC cells was cultured for 0, 1 and 2 days in a culture medium containing the exosomes at a concentration of 1×109 exosomes/ml according to the method of Example 6, and the telomere length and telomerase activity in each type of cells were analyzed. As a result, it could be confirmed that, in all the four types of cells tested, telomeres were significantly elongated and telomerase activity was also high (
To further verify telomere elongation, staining with a Cy3-labeled PNA telomere probe (complementary to the telomere repeat sequence SEQ ID NO: 6, TTAGGG) and Hoechst33342 was performed. At this time, as a pretreatment before the experiment, medium was treated with Colcemid for 48 hours to fix the cells to the division metaphase in which intranuclear chromosomes are generated. Then, the chromosome in the cell nucleus was mounted onto slide glass using a low osmotic pressure medium and a fixative, and then a solution containing hybridization buffer and a PNA probe (pre-warmed to 90° C.) was added to the chromosome, and then the cells were incubated at 85° C. for 10 minutes, and then cooled slowly at room temperature for 1 hour. Then, the cells were washed with 2×SSC buffer and stained with the nuclear staining reagent Hoechst 33342, followed by mounting. Then, expression of telomere fluorescence compared to the chromosome was analyzed with a confocal laser microscope at 1,000× magnification. As a result, as shown in
Next, the frequency of repeat sequences at telomere ends was analyzed through whole genome sequencing. First, as a result of analyzing the frequency of the SEQ ID NO: 6, TTAGGG sequence, it could be confirmed that the SEQ ID NO: 6, TTAGGG sequence appeared more frequently in the cell group cultured in the culture medium containing the exosomes at a concentration of 1×109 exosomes/ml for 2 days than in the control group not treated with the exosomes (
To identify RNAs in the cells treated with the exosomes according to the method of Example 6, RNA-seq was performed and gene ontology analysis was performed. As a result, it was confirmed that a number of genes associated with telomere elongation, telomerase activity, cell cycle and proliferation, and metabolism were present in the cells (
Next, in order to confirm the expression of TERT in the cells treated with the exosomes according to Example 6, qPCR and immunofluorescence staining were performed after 0, 1 and 2 days exosome treatment. As a result, it was confirmed that the amounts of TERT RNA and protein increased as the exosome treatment time increased (
In order to determine how the change in gene expression in cells treated with the ultrasound-induced exosomes affects cell proliferation, HDFs were cultured for 0, 1 and 2 days in a medium containing the exosomes according to the method of Example 6, and then fluorescence-stained using anti-Ki67 antibody, followed by analysis with a confocal microscope (at this time, the cells were counter-stained with Hoechst). As a result, as shown in
In addition, in order to examine how the concentration of the exosome affects cell proliferation, HDFs were cultured for 2 days in a medium containing the exosomes at a concentration of each of 0, 1, 2 and 4 (×109 exosome particles/ml), then fluorescence-stained using anti-Ki67 antibody, followed by analysis with a confocal microscope (at this time, the cells were counter-stained with Hoechst). As a result, as shown in
In order to examine how the change in gene expression in cells treated with the ultrasound-induced exosomes affects cell senescence, HDFs were cultured for 0, 1 and 2 days in a medium containing the exosomes according to the method of Example 6, a test for β-galactosidase activity known to have a correlation with intracellular senescence was performed using X-gal, followed by analysis with a phase contrast microscope. As a result, as shown in
In order to examine how the application of the ultrasound-induced exosomes to animals has on the telomere length, 1×109 and 1×1010 exosomes produced according to Example 5 were applied to one ear of 10-week-old ICR mice three times a week, and ear samples were collected at 1 week and 2 weeks, respectively, and the telomere length and the TERT RNA expression level therein were analyzed. At this time, as a control, the opposite ear to which D-PBS containing the exosomes diluted therein was applied was used, and the control is indicated as 0 in
As described above, it was found that the exosomes produced according to the production method of the present invention exhibit effects such as telomere elongation and cell proliferations. Since these effects are highly correlated with cell regeneration, the effects of these exosomes on skin regeneration, wound healing and scar healing were evaluated. First, in order to examine what effect the exosomes have on the migration of cells, the exosomes produced according to Example 5 were added to a medium, and HDFs were cultured in the medium to fill the plate, and then wound healing assay was performed by creating lines by a 20 μl yellow tip to separate the cells at a distance from one another, and then treating the cells with the exosomes at concentrations of 0, 5, 10 and 20 (×109) exosomes/ml, followed by culture. As a result, it was confirmed that the empty space in the exosome-treated group was filled relatively quickly as the exosome concentration increased (
Next, in order to evaluate the effects of the exosome in vivo, a 6-mm wound was created on the skin of each 6-week-old C57 mouse using a punch, and the exosomes were diluted in PBS at concentrations of 0, 5, 10 and 20×109 exosomes/ml and applied to each wound site twice a week. As a result, it was confirmed that the size of the externally exposed wound (opening) in the exosome-treated mice after 1 week significantly decreased compared to that in the untreated mice. In addition, after 1 week and 2 weeks, the tissue section of each wound site was analyzed by H & E staining. As a result, it could be confirmed that the wound size in the exosome-treated mice was smaller than that in the non-exosome-treated mice, and thus skin regeneration, wound healing and scar healing occurred more quickly in the exosome-treated mice compared to the non-exosome-treated mice. In particular, when the wound site was treated with the exosomes at a concentration of 10 or 20×109 exosomes/ml, the skin tissue was completely recovered at week 2, and thus the epidermis, dermal layer, fat layer and muscle layer constituting the skin tissue were regenerated so that they could be clearly distinguished from one another. In addition, in this case, hair follicles, which are skin appendages, were located in the dermal layer and the fat layer without any difference between the wound site and the surrounding area (
In addition, the exosomes were stained with Vybrant™DiD cell-labeling solution and the skin was treated with the stained exosomes, and after 2 weeks, the site treated with the stained was analyzed under a fluorescence microscope. As a result, it could be confirmed that the exosomes penetrated the entire wound site, and the above-described effects could appear due to this penetration into the entire wound site (
Taken together, it could be confirmed that the exosomes produced by the production method of the present invention could have skin regeneration, wound healing and scar healing effects not only in vitro but also in vivo.
As described above, it was found that the exosomes produced according to the method of the present invention induced expression of various genes related to anti-aging. To examine these exosomes can have an effect even on senescence-accelerated cells, fibroblasts derived from a patient with progeria were treated with the exosomes, and the telomere length, telomerase activity, TERT expression, cell proliferation, Ki67 expression, and senescence-related β-galactosidase activity in the cells were analyzed. The cells used herein were cells isolated from the thigh skin of a patient with Hutchinson-Gilford progeria syndrome (White/8 years old/male) (AG06297, Coriell Institute, Camden, USA). The cells were treated with the exosomes at a concentration of 1×109 exosomes/ml, and the cells were analyzed 14 days after the initial treatment. The experiment was conducted on the following two groups: an experimental group (ReprosomeX1) treated once at the beginning; and an experimental group (ReprosomeX∞, treated 4 times for 14 days) using a medium containing the above-described concentration of exosomes at every medium replacement.
As a result, it could be confirmed that, in both the experimental group treated with the exosomes once at the beginning and the experimental group continuously treated with the exosomes, telomeres were elongated, telomerase activity increased, TERT gene expression increased (
The above description of the present invention is exemplary, and those of ordinary skill in the art will appreciate that the present invention can be easily modified into other specific forms without departing from the technical spirit or essential characteristics of the present invention. Therefore, it should be understood that the embodiments described above are exemplary in all aspects and are not restrictive. For example, each component described to be of a single type can be implemented in a distributed manner. Likewise, components described to be distributed can be implemented in a combined manner.
The scope of the present invention is defined by the appended claims, and it shall be understood that all modifications and alterations conceived from the meaning and scope of the claims and equivalents thereto are included in the scope of the present invention.
The exosomes for elongating telomeres of cells according to the present invention and a composition containing the same elongate telomeres, induce cell division, have anti-aging and tissue regeneration, and thus may be used as drugs that may prevent, ameliorate and treat not only problems caused by shortening of telomeres, but also various diseases and conditions associated with aging and tissue regeneration. The exosomes and the composition containing the same may exhibit their effects even when they are applied in small amounts in a noninvasive manner.
In addition, the method for producing exosomes for elongating telomeres of cells according to the present invention is a method capable of loading various factors having the above-described effects into exosomes, which can penetrate cells, by simply treating cells with physical stimulation. Through this method, exosomes containing high concentrations of active ingredients may be obtained in high yield
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2018-0117265 | Oct 2018 | KR | national |
| 10-2019-0115381 | Sep 2019 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2019/012150 | 9/19/2019 | WO | 00 |
