Yoshii H, Watanabe K, Yanagihara Y, Shida T
Nihon Yakurigaku Zasshi. 1984 Dec;84(6):499-507. doi: 10.1254/fpj.84.499.
It was reported that neurotropin (NSP), an extract isolated from the inflamed skins of rabbits inoculated with vaccinia virus, activates murine T cell functions participating in cell-mediated immunity. The present study was undertaken to examine the effect of NSP on plastic dish-adherent macrophages (M phi) from ddY mice in vitro. Total activities of beta-glucuronidase and N-acetyl-beta-D-glucosaminidase in resident peritoneal M phi was slightly enhanced when the M phi were cultured with NSP (10-1000 micrograms/ml) for 48 and 96 hr, but no enhancement was noted in 24 hr culture. Intracellular activity of lactate dehydrogenase (LDH) was also strongly enhanced in a dose-dependent manner by culturing with NSP for 48 and 96 hr. The enhanced LDH activity in the M phi cultured with NSP for 96 hr was completely inhibited by cycloheximide, an inhibitor of protein synthesis. In addition, consumption of glucose in the culture media by the M phi was also enhanced by culturing with NSP for 96 hr. Intracellular activity of LDH and glucose consumption of plastic dish-nonadherent cells from normal mouse peritoneal cells, however, was not enhanced by NSP in 96 hr culture. In regard to allogeneic M phi-mediated cytostatic activity to P815-X2 mastocytoma, NSP had no effect on cytostatic activities of the resident and thioglycollate-induced M phi, although NSP by itself dose-dependently inhibited the growth of P815-X2 mastocytoma without affecting cell viability. These results suggest that NSP biochemically activates mouse peritoneal M phi in vitro, but the M phi activated by NSP can not inhibit the growth of P815-X2 mastocytoma.
据报道,神经妥乐平(NSP)是从接种痘苗病毒的兔子发炎皮肤中分离出的一种提取物,可激活参与细胞介导免疫的小鼠T细胞功能。本研究旨在体外检测NSP对ddY小鼠塑料培养皿贴壁巨噬细胞(M phi)的影响。当M phi与NSP(10 - 1000微克/毫升)培养48小时和96小时时,驻留腹膜M phi中β-葡萄糖醛酸酶和N-乙酰-β-D-氨基葡萄糖苷酶的总活性略有增强,但在24小时培养中未观察到增强。通过与NSP培养48小时和96小时,乳酸脱氢酶(LDH)的细胞内活性也以剂量依赖的方式强烈增强。用NSP培养96小时的M phi中增强的LDH活性被蛋白质合成抑制剂环己酰亚胺完全抑制。此外,通过与NSP培养96小时,M phi对培养基中葡萄糖的消耗也增加。然而,在96小时培养中,NSP并未增强正常小鼠腹膜细胞中塑料培养皿非贴壁细胞的LDH细胞内活性和葡萄糖消耗。关于同种异体M phi对P815-X2肥大细胞瘤的细胞抑制活性,NSP对驻留和巯基乙酸诱导的M phi的细胞抑制活性没有影响,尽管NSP本身剂量依赖性地抑制P815-X2肥大细胞瘤的生长而不影响细胞活力。这些结果表明,NSP在体外可生物化学激活小鼠腹膜M phi,但被NSP激活的M phi不能抑制P815-X2肥大细胞瘤的生长。