Genetic factors influencing murine hematopoietic productivity in culture

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Abstract
In order to study a previously described genetic difference manifested in stem cell kinetics of specific mouse strains, effects of this putative gene, stk, were measured on growth and expansion of stem and progenitor cell populations ex vivo. Bone marrow cells from each of two inbred mouse strains, C57BL/6J and DBA/2J, were placed into separate bioreactor cultures perfused continuously with growth medium containing erythropoietin (Epo), interleukin‐3 (IL‐3), granulocyte‐macrphage colony stimulating factor (GM‐CSF), and Kit ligand as well as 5% CO2. Expansion of cell numbers reached 20‐fold for DBA/2J and 10‐fold for C57BL/6J marrow within about 1 week of culture. Significant production was also seen of colonyforming unit (CFU)‐GM (up nine‐fold from input levels) just prior to the cell production peak, and, importantly, moderate expansion of day 12 colony‐forming unit‐spleen (CFU‐S; two‐ to threefold) occurred as well, although CFU‐S production peaked at a relatively short 4 days. CFU‐S and CFU‐GM levels declined rapidly in culture, either because of unfavorable growth conditions or terminal differentiation. Attempts to remove toxic metabolites by increasing the media perfusion rate resulted in a boost in cell expansion capability by DBA/2J marrow. In bioreactors in which stromal cells were established before marrow inoculation, there was greater expansion of CFU‐S (especially by DBA/2J) and CFU‐GM, although total cell yield appeared to be unaffected, perhaps because the maximum cell density had already been reached. The relative high potential for CFU‐S expansion measured in DBA/2J marrow over that of C57BL/6J will be useful in following genetic contributions to bone marrow production capacity.

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