Wilton J M, Rosenstreich D L, Oppenheim J J
J Immunol. 1975 Jan;114(1 Pt 2):388-93.
The activation of guinea pig peritoneal macrophages by Salmonella typhimurium lipopolysaccharide (LPS) was studied by using 14C-glucosamine uptake. Peritoneal exudate cells incorporated significant amounts of 14C-glucosamine when stimulated with LPS but neither purified macrophages nor nonadherent lymphocytes by themselves incorporated glucosamine. The activation of macrophages could be restored by adding nonadherent peritoneal lymphocytes, spleen cells, and lymph node cells but not thymocytes. Removal of B lymphocytes abolished the restorative capacity from active lymphoid cell populations. In contrast, B lymphocytes would restore glucosamine incorporation by macrophages stimulated with LPS but T lymphocytes did not. In addition, cell-free supernatants from LPS stimulated B lymphocytes but not from T lymphocytes could restore glucosamine incorporation by macrophages. These experiments demonstrate that LPS does not directly activate macrophages as measured by glucosamine incorporation but stimulates B lymphocytes which in turn activate macrophages.
通过使用¹⁴C - 葡糖胺摄取研究了鼠伤寒沙门氏菌脂多糖(LPS)对豚鼠腹腔巨噬细胞的激活作用。当用LPS刺激时,腹腔渗出细胞摄取了大量的¹⁴C - 葡糖胺,但纯化的巨噬细胞或非黏附淋巴细胞自身均不摄取葡糖胺。添加非黏附腹腔淋巴细胞、脾细胞和淋巴结细胞可恢复巨噬细胞的激活,但胸腺细胞不能。去除B淋巴细胞消除了活性淋巴细胞群体的恢复能力。相反,B淋巴细胞可恢复LPS刺激的巨噬细胞的葡糖胺摄取,但T淋巴细胞不能。此外,LPS刺激的B淋巴细胞而非T淋巴细胞的无细胞上清液可恢复巨噬细胞的葡糖胺摄取。这些实验表明,以葡糖胺摄取衡量,LPS不会直接激活巨噬细胞,而是刺激B淋巴细胞,进而激活巨噬细胞。