Kalechman Y, Sredni B, Caspi R R, Nussenblatt R B
Department of Life Sciences, Bar Ilan University, Ramat Gan, Israel.
Exp Hematol. 1990 Nov;18(10):1104-7.
The development of the number of colonies (cell colony-forming units, CFU-C) in soft agar from normal mouse bone marrow (BM) cells was enhanced 60% when total bone marrow cells (BMC) were preincubated for 1 h with either cyclosporin A (CsA) or cyclosporin G (CsG) before plating. Using cell fractionation techniques we found that the removal of macrophages enhanced CFU-C in noncyclosporin-treated BM and that cyclosporins mediated an additional enhancing effect. A similar enhancing effect on CFU-C in noncyclosporin-treated BM was obtained by depleting it of total T cells or Lyt-2.2+ cells. However, CFU-C growth in the residual BM population was no longer enhanced by cyclosporin. Conversely, removal of Lyt-1.2+ cells did not enhance CFU-C in noncyclosporin-treated BM, but the CFU-C in this population were enhanced by cyclosporin treatment. These results suggest that CsA and CsG can increase the cloning efficiency of normal mouse BMC, possibly by inhibiting an endogenous Lyt-2.2+ suppressor cell.
在接种前,将正常小鼠骨髓(BM)细胞与环孢素A(CsA)或环孢素G(CsG)预孵育1小时,可使软琼脂中集落数量(细胞集落形成单位,CFU-C)的发育增强60%。使用细胞分级分离技术,我们发现去除巨噬细胞可增强未用环孢素处理的BM中的CFU-C,且环孢素介导了额外的增强作用。通过耗尽总T细胞或Lyt-2.2+细胞,在未用环孢素处理的BM中对CFU-C也获得了类似的增强作用。然而,环孢素不再增强残余BM群体中的CFU-C生长。相反,去除Lyt-1.2+细胞并未增强未用环孢素处理的BM中的CFU-C,但该群体中的CFU-C通过环孢素处理得到增强。这些结果表明,CsA和CsG可能通过抑制内源性Lyt-2.2+抑制细胞来提高正常小鼠BMC的克隆效率。