Cryopreservation medium and cryopreservation method for tissues and cells

Abstract

A cryopreservation medium and a cryopreservation method which make it possible to cryopreserve tissues and cells with high viability are provided. A cryopreservation medium contains polyphenol at a concentration of from 30 to 120 ppm. In an embodiment, a cryopreservation method for tissues and cells comprises: incubating tissues or cells for 2 hours in culture medium supplemented with polyphenol at concentrations of from 30 to 120 ppm; suspending tissues or cells in a cryopreservation medium; freezing the suspension of the tissues or cells in the cryopreservation medium; and storing the frozen suspension of tissues or cells in the cryopreservation medium.

Description

FIELD OF THE INVENTION

The present invention relates to a cryopreservation medium and a cryopreservation method for tissues and cells, which have the potential to promising applications in the fields of cell culture, cell and tissue transplantation and research for embryonic stem (ES) cells

BACKGROUND OF THE INVENTION

Dimethyl sulfoxide (DMSO) is the most frequently used cryoprotectant in islet cell cryopreservation. The cryopreservation method used most frequently is slow cooling to −40° C. and rapid thawing from −196° C.¹.

However, the cells established by the above method have a problem of poor cryopreservation efficiency under the conventional cryopreservation conditions mainly used for islets cells.

Polyphenol has several bioactivity like antioxidant, radical scavenger and anti-apoptosis besides antimicrobial, deodorant, anti-cancer and anti-viral². These bioactivity is thought to be effective to prevent from freeze and thaw injury.

The object of the present invention is to provide a cryopreservation medium and a cryopreservation method which make it possible to cryopreserve tissues and cells with high viability.

BRIEF SUMMARY OF THE INVENTION

The present inventors have carried out studies to solve the above-mentioned problems and have completed the present invention on the basis of the finding that the use of a cryopreservation medium containing polyphenol as a cryoprotectant at a concentration of from 10 to 300 ppm, allows cryopreservation of tissues and cells with high viability.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING

FIG. 1 shows recovery rates of islets following cryopreservation and after 48 hours of postcryopreservation tissue culture in 4 groups in Example.

FIG. 2 is islet viability of post-cryopreservation islets in 4 groups in Example.

FIG. 3 is functionality of post-cryopreservation islets in 4 groups in Example.

DETAILED DESCRIPTION OF THE INVENTION

Materials and Methods

Islets were isolated from over two years old pigs (n=3). After overnight culture, a known number of islets were incubated for 2 hours in culture medium supplemented with polyphenol (epigallocatechin-gallate (EGCg) with more than 98% purity) at concentrations of 0 (control), 30, 60, 120 ug/ml. Islets were suspended in the same volume of cryopreservation solution containing 12% hydroxyethyl starch (HES) and 10% dimethyl sulfoxide (DMSO) with 8% fetal blood serum (FBS), and then cryopreserved using a program freezing system³. After 4 weeks storage in liquid nitrogen, islets were rapidly thawed in a hot water bath. We assessed the results on recovery rate (islet yield after thawing/islet yield before freezing) following cryopreservation and after 48 hours of postcryopreservation tissue culture, viability and functionality.

EXAMPLE

As shown in FIG. 1, islet recovery rates following cryopreservation were 49.3±1.6%, 66.5±3.3%, 76.9±5.2%, 74.5±2.9% in groups 0, 30, 60, 120 ug/ml of polyphenol, respectively. Islet recovery rates after 48 hours of postcryopreservation tissue culture were 25.2±3.6%, 45.3±0.3%, 68.0±3.0%, 54.6±3.3%, respectively. Islet recovery following cryopreservation in the polyphenol group were significantly higher than the control group (p<0.01).

As shown in FIG. 2, viability assessed using AO/PI were 71.3±3.4, 83.1±1.2, 85.9±2.5, 84.4±1.0 respectively. Viability following cryopreservation in the polyphenol group were significantly higher than the control group (p<0.01).

As shown in FIG. 3, Functionality indicated by stimulation index was 1.2±0.1, 1.4±0.2, 1.4±0.3, 0.9±0.3, respectively. The stimulation index represents a ratio of insulin secretion between high-concentration glucose culture medium and low-concentration glucose culture medium.

LIST OF REFERENCES CITED

• 1. Corominola H, Mendola J, et al. Cryopreservation of pancreatic islets prior to transplantation: A comparison between UW solution and RPMI culture medium. CRYOBIOLOGY 1998; 37: 110-118.
• 2. Hyon, S.-H. et al. (2005) Protection of human fibroblasts from reactive oxygen species by green tea polyphenolic compounds. Key Engineering Materials 288-9:665-668.
• 3. Maruyama M, Kenmochi T, et al: Simplified method for cryopreservation of islets using hydroxyethyl starch and dimethyl sulfoxide as cryoprotectants. Transplantation Proceedings 2004; 36: 1133-1134.

Claims

1-2. (canceled)

3. A cryopreservation medium for tissues and cells for transplantation effective in preventing freeze and thaw injury, comprising polyphenol as a cryoprotectant at a concentration of from 30 to 120 ppm (parts per million) and further comprising dimethyl sulfoxide and/or glycerin as a cryoprotectant.

4. A cryopreservation medium for tissues and cells for transplantation effective in preventing freeze and thaw injury, comprising polyphenol as a cryoprotectant at a concentration of from 30 to 120 μm, and further comprising dimethyl sulfoxide as a cryoprotectant at a concentration from 5% (W/V) to 20% (W/V).

5. A cryopreservation medium for tissues and cells for transplantation effective in preventing freeze and thaw injury, comprising polyphenol as a cryoprotectant at a concentration of from 30 to 120 ppm, and further comprising hydroxyethyl starch (HES) as a cryoprotectant at a concentration from 5% (W/V) to 20% (W/V).

6. (canceled)

7. A cryopreservation medium for tissues and cells for transplantation effective in preventing freeze and thaw injury, comprising polyphenol as a cryoprotectant at a concentration of from 30 to 120 ppm, and further comprising, in addition to the cryoprotectant, serum and/or a serum replacement, a basal medium for animal tissue culture containing at least from 0.3% (W/V) to 5% (W/V) of glucose, at a concentration of from 10% (W/V) to 75% (W/V).

8-9. (canceled)

10. A cryopreservation method for islets isolated from humans and animals comprising: incubating said islets in culture medium supplemented with polyphenol at concentrations of from 10 to 300 ppm; suspending said islets in a cryopreservation medium; freezing the suspension of said islets in the cryopreservation medium by cooling them; and storing the frozen suspension of said islets in the cryopreservation medium.

11.-13. (canceled)