Ramsey R, Hays E F
Exp Hematol. 1979 May;7(5):245-54.
The regulation of colony stimulating activity (CSA) release from CSA producing cells is a poorly understood process. Using freshly isolated mouse peritoneal cells and a continuous line of mouse thymic epithelial cells a precise and reproducible method of short term culture was developed to study this phenomenon. Serum, endotoxin, lithium, and cyclic GMP stimulated CSA release from both cell types. Particles such as zymosan, inulin, latex, and iron filings stimulated CSA release from mouse peritoneal cells but not from thymic epthelial cells. Theophylline and cyclic AMP inhibited CSA release from both cell types. Trypsin activated guinea pig C3 and C5 did not stimulate CSA release. Cycloheximide, an inhibitor of protein synthesis, completely inhibited CSA release. We believe these findings may reflect mechanisms of in vivo regulation of CSA release.
集落刺激活性(CSA)产生细胞释放CSA的调控是一个尚不清楚的过程。利用新鲜分离的小鼠腹腔细胞和小鼠胸腺上皮细胞系,开发了一种精确且可重复的短期培养方法来研究这一现象。血清、内毒素、锂和环鸟苷酸刺激这两种细胞类型释放CSA。诸如酵母聚糖、菊粉、乳胶和铁屑等颗粒刺激小鼠腹腔细胞释放CSA,但不刺激胸腺上皮细胞释放。茶碱和环磷酸腺苷抑制这两种细胞类型释放CSA。胰蛋白酶激活的豚鼠C3和C5不刺激CSA释放。蛋白质合成抑制剂环己酰亚胺完全抑制CSA释放。我们认为这些发现可能反映了体内CSA释放的调控机制。