The invention relates to a substructure for cultivating cells, comprising well-like culture sites separate from each other. The invention relates particularly to a so-called well plate. The invention also relates to the use of the cultivation substructure.
Cell cultures are generally used e.g. in various cytobiological and biomedical analyses. Typically, the cell material to be analyzed is cultured in a Petri dish or on a well plate placed in suitable conditions with respect to the temperature, ambient gas and illumination. At various stages of the analyses, the samples are subjected to, for example, microscopy, and in arrangements of prior art, the well plate is arranged to be examined with a microscope which may be equipped with a camera. In many studies, the same samples are examined at regular intervals so that the development of the cell can be monitored.
From patent documents, a number of apparatuses are known which have been constructed in such a way that cells to be cultured in a sub-structure, for example in a well plate, can be kept in desired culturing environment (temperature, culture medium, atmosphere). To monitor the development of cells, for example their growth and/or the way in which they are affected by given substances added in the culture medium, it is necessary to take images at different sites of the cultivation substructure in such a way that the same sites (for example, separate wells) are imaged at regular intervals according to a given schedule.
In the simplest form, the imaging is carried out by taking the cultivation substructure out of the culturing chamber (e.g. incubator) and placing it onto a particular microscope base where the imaging can be carried out automatically, manipulators moving the base with respect to the objective of the microscope. The images thus taken are recorded in a memory and they can be processed later on. In a more automated version, the cultivation substructures are automatically removed from the incubator to be imaged according to a predetermined program. An apparatus for implementing this is presented e.g. in U.S. Pat. No. 5,106,584.
The removal of the cultivation substructures from the incubator for imaging may be a disturbing factor, because the cultivation substructure with the cells is removed from the environment where the conditions have been adjusted to be optimal, and it may also be subjected to bumps when it is being moved from one base to another. Therefore, apparatuses are also known for carrying out the imaging when the cultivation substructure is in the incubator. For example, U.S. Pat. No. 6,271,022 discloses an apparatus in which the imaging is arranged inside the incubator in such a way that substructures placed on shelves on top of each other can be imaged one after the other, although accurate imaging is not achieved by this method.
U.S. Pat. No. 6,008,010 presents an apparatus in which a well plate is placed on top of the transparent bottom of a closed incubator chamber. The cover of the incubator chamber is transparent as well, wherein imaging can be performed in the vertical direction through the incubator chamber by using a manipulator to move the whole chamber in the horizontal direction in relation to the imaging optics. With this system, it is already possible to perform imaging in situ without removing the cultivation substructure from the chamber. However, a problem lies in the fact that the whole culture chamber must be moved. Because of this, the culture chamber, or “biochamber”, has been made relatively small (length×width×height 6″×5″×2″). Moreover, the use of a transparent extra plate under the bottom of the well plate is problematic for high magnifications, because the objective must be brought very close to the object.
Consequently, it is known to place well plates in an incubator having desired ambient conditions (humidity, temperature, gas composition). For example, an incubator chamber according to U.S. Pat. No. 6,271,022 containing several cultivation substructures in shelves is arranged to be air-tight to provide a given CO2 level inside the chamber. It is difficult to provide such uniform conditions for all the cultivation substructures. One problem is, for example, the control of humidity. Furthermore, as the cultivation substructure is removed from the incubator, it is exposed to external conditions, which may be harmful if the cultivation substructure must be removed for any reason.
It is an aim of the invention to eliminate the above-mentioned drawbacks and to present a cultivation substructure which constitutes a compact unit and in which the desired conditions can be maintained better. To achieve this aim, the cultivation substructure according to the invention is primarily characterized in that the cultivation substructure is closed hermetically from above with a lid which, together with the substructure, limits an air space being common to the culture sites and having a gas inlet and a gas outlet, and that water has been added onto the bottom of the cultivation substructure in the areas outside the culture sites, to maintain humidity in the air space. The humidity prevents the drying of the wells.
In this way, a kind of a mini incubator can be formed of the cultivation substructure by connecting to it a lid with an inlet and an outlet provided ready for a gas. Via the inlet, it is possible to supply a desired gas composition, for example a composition with a desired content of oxygen and/or carbon dioxide. Most commonly, the carbon dioxide content of 5% is used in the air to be supplied. The outlet can be connected to a check valve letting gas through in one direction only, away from the air space. It is possible to use a normal well plate which can be easily converted to said mini incubator by means of the invention.
With respect to the maintenance of the gas composition and humidity, the mini incubator can be placed as a separate, independent unit in a larger incubator chamber. To image cells on the cultivation substructure in the incubator environment at given intervals, the imaging optics and the unit can be moved in relation to each other in the incubator chamber, wherein the different culture sites (wells) are imaged.
In the following, the invention will be described in more detail with reference to the appended drawings, in which
The well plate 3 is closed from above with a lid 3b in an air-tight manner. The lid 3b comprises downwards extending edges (a flange) by means of which the lid can be fixed to the plate by pressing, and by sealing the joint it is possible to produce a mini incubator isolated from the environment. The lid is also provided with an inlet and an outlet, through which a gas can be introduced into the closed air space underneath the lid 3b, and be removed from it, respectively. The gas inlet and outlet ducts are marked with reference numerals 7 and 8, respectively. The outlet duct 8 comprises a valve 9 which prevents an air flow from the environment into the mini incubator but lets gas out. A pump or a gas bottle and adjustable valves, are provided at the initial end of the inlet duct 7 to supply a gas with a desired composition at intervals into the mini incubator.
Generally, the gas is air with a carbon dioxide content higher than in normal air, to buffer the culture medium in the wells 10. Normally, the content of 5% is used. It is possible that instead of or in addition to carbon dioxide, the content of another gas component should be set to a desired level, for example the oxygen content.
Water has been added onto the bottom of the well plate in the space between the wells. The purpose of this water is to keep the air in the mini incubator humid. Consequently, drying of the wells is avoided, and it is not necessary to control the humidity of the air to be supplied.
Both the bottom 3a and the lid 3b of the well plate are made of a transparent material, for example optically clear plastic, wherein microscopic imaging in the vertical direction through the well plate is possible.
The temperature of the mini incubator can be adjusted by placing it in a larger chamber whose temperature is controlled.
The culture chamber 1 constitutes a dark chamber protected from ambient light, and its temperature can also be adjusted to a desired level irrespective of ambient temperature. The arm 2 is introduced via a through-hole in the side of the chamber, sealed with e.g. elastic means so that no light or heat can enter through the hole but the arm 2 can move in the hole. Similarly, the microscope 4 is introduced into the culture chamber 1 via a sealed opening (sealing ring 11).
According to the above-mentioned principle, it is possible to provide the mini incubator 3 with a desired gas composition, irrespective of the gas composition inside the culture chamber 1.
Imaging is performed in the normal way, one well 10 of the well plate at a time, wherein several sites of a single well can be imaged. The well 10 of the well plate to be imaged is determined by means of the manipulator moving the mini incubator 3 in the X-Y plane. Furthermore, in each well it is possible to take images from different sites in the Z direction by moving the microscope in a direction perpendicular to the X,Y plane, for example to take a series of images of the same well in different focusing planes. During the imaging, the illumination can be provided by using illumination whose duration is set accurately with a system presented in more detail in a parallel patent application “An illumination system for a microscope” filed simultaneously.
The alternatives relating to the storage and processing of the image itself do not fall within the scope of the present invention, and they will thus not be disclosed in more detail.
However, the invention can also be applied elsewhere than in the environment shown in
Number | Date | Country | Kind |
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20040971 | Jul 2004 | FI | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/FI05/50277 | 7/8/2005 | WO | 12/8/2006 |