Thursday, 18 June 2015

Development of media for animal tissue culture



DEVELOPMENT OF MEDIA FOR ANIMAL TISSUE CULTURE

Initially the attempt to culture (animal) cells was performed in natural media based on tissue extracts and body fluids, such as chick embryo extract, lymph, serum etc. With the propagation of cell lines, the demand for larger amounts of a medium of more consistent quality led to the introduction of chemically defined media based on analyses of body fluids and nutritional biochemistry. Eagle’s Basal Medium and subsequently, Eagle’s Minimal Essential Medium (MEM) became widely used mediums, these were supplemented with horse, human, or calf serum, protein hydrolysates and extracts from embryo. As more continuous cell lines became available (HeLa, L929 cells etc.), it was assumed that these media were perfect and adequate for most of these cell lines, and most of the later developments were aimed to replace serum, optimizing media for different cell types (e.g., RPMI 1640 for lymphoblastoid cell lines), or modifying for specific conditions (e.g., Leibovitz L15 to eliminate the need for adding CO2 and NaHCO3).
Isolation and propagation of cells of a specific cell line may require a selective serum-free medium, whereas cells grown for the formation of products, as hosts for viral propagation, or for non-cell-specific molecular studies rely mainly on Eagle’s MEM, Dulbecco’s modification of Eagle’s medium, DMEM or even RPMI 1640, supplemented with serum. However, many industrial-scale production techniques now use serum-free media, to facilitate downstream processing and reduce the risk of adventitious infectious agents. A popular compromise for many laboratories is a mixture of a complex medium, such as Ham’s F12 with higher amino acid and vitamin concentrations, such as DMEM. This alternative may not be always acceptable but it generates a useful and all-purpose medium for primary culture as well as cell line propagation.

We will study the different types of media in our next post.

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