Shands J W
Blood. 1985 Jan;65(1):169-75.
The in vitro production of factor VII-like material and of tissue factor activity by murine thioglycollate exudate macrophages was measured by amidolytic assays. Tissue factor activity was inducible by endotoxin, and its induction was inhibited by 1 microgram/mL of actinomycin D, 10 micrograms/mL of cycloheximide, and 0.2 micrograms/mL of tunicamycin. Soluble factor VII-like material was secreted by macrophages into culture supernatants. The amount produced was not influenced by further activation of the cells by endotoxin, nor was its production inhibited significantly by 1 microgram/mL actinomycin D or 0.2 micrograms/mL tunicamycin. The production of the factor VII-like material was inhibited by 10 micrograms/mL of cycloheximide, and its appearance in culture supernatants was enhanced significantly by the addition of vitamin K1. When lysates of activated macrophages were suspended in ultracentrifuged culture supernatants, a particulate factor X activator was formed. Centrifugation at 100,000 g pelleted the factor X activator and left no factor VII-like material in the supernatant. The data indicate that thioglycollate-induced exudate macrophages make and excrete factor VII-like material, and this production is not modulated by further activation. However, activation of the macrophages induces tissue factor production. The factor X activator appears to result from the interaction and complexing of the soluble factor VII-like material and the membrane-bound tissue factor.
通过酰胺水解测定法测量了小鼠巯基乙酸盐渗出液巨噬细胞体外产生的VII因子样物质和组织因子活性。内毒素可诱导组织因子活性,其诱导作用可被1微克/毫升放线菌素D、10微克/毫升环己酰亚胺和0.2微克/毫升衣霉素抑制。可溶性VII因子样物质由巨噬细胞分泌到培养上清液中。产生的量不受内毒素对细胞进一步激活的影响,1微克/毫升放线菌素D或0.2微克/毫升衣霉素也不会显著抑制其产生。10微克/毫升环己酰亚胺可抑制VII因子样物质的产生,添加维生素K1可显著增强其在培养上清液中的出现。当将活化巨噬细胞的裂解物悬浮于超速离心的培养上清液中时,会形成一种颗粒状的因子X激活剂。以100,000g离心可使因子X激活剂沉淀,上清液中不再有VII因子样物质。数据表明,巯基乙酸盐诱导的渗出液巨噬细胞产生并分泌VII因子样物质,且这种产生不受进一步激活的调节。然而,巨噬细胞的激活会诱导组织因子的产生。因子X激活剂似乎是由可溶性VII因子样物质与膜结合组织因子相互作用并形成复合物所致。