Jutila M A, McIvor K L
J Leukoc Biol. 1986 May;39(5):533-45. doi: 10.1002/jlb.39.5.533.
Macrophages produced and/or released a chemoattractant(s) for neutrophils after having been treated for 2 hr with soluble products from two lymphoma cell lines. Culture supernatants of the EL-4 and Yac-1 cell lines, but not sarcoma l, Bc100, or the macrophagelike cell line P388d1, triggered the release of the chemoattractant. The macrophage-derived chemoattractant (MDC) was detectable within 2 hr following triggering and culture supernatants had maximal activity by 48 hr. The triggering of the macrophages to release the chemoattractant and the activity of the chemoattractant was not dependent upon any component of fetal bovine serum. Activation of complement was also not involved, since activated serum did not competitively inhibit the chemotactic activity of the macrophage-derived chemoattractant. The chemoattractant was macromolecular, stable to heating at 90 degrees C for 15 min, sensitive to pronase and chymotrypsin, and was affected by treatment with low pH.
巨噬细胞在经两种淋巴瘤细胞系的可溶性产物处理2小时后,产生和/或释放了一种吸引中性粒细胞的趋化因子。EL-4和Yac-1细胞系的培养上清液能触发趋化因子的释放,但肉瘤1、Bc100或巨噬细胞样细胞系P388d1的培养上清液则不能。触发后2小时内可检测到巨噬细胞衍生趋化因子(MDC),培养上清液在48小时时活性达到最大。巨噬细胞释放趋化因子的触发过程以及趋化因子的活性并不依赖于胎牛血清的任何成分。补体激活也未参与其中,因为激活的血清不会竞争性抑制巨噬细胞衍生趋化因子的趋化活性。该趋化因子是大分子物质,在90摄氏度加热15分钟后稳定,对链霉蛋白酶和胰凝乳蛋白酶敏感,且受低pH处理的影响。