Rosenstreich D L, Vogel S N, Jacques A R, Wahl L M, Oppenheim J J
J Immunol. 1978 Nov;121(5):1664-70.
The effects of LPS on macrophages in vitro have been examined. LPS triggers macrophages to produce LAF and PGE2 in vitro. LPS is also cytotoxic for macrophages derived from LPS-sensitive mice and will significantly inhibit their phagocytic ability. Both LAF production and cytotoxicity are due to the direct effects of LPS on the macrophage and do not require the particpation of lymphocytes. Each of these functions is abnormal in C3H/HeJ mice. The nature of the gene(s) controlling these macrophage responses to LPS has been determined. The response of (C3H/HeJ X C3H/HeN)F1 macrophages was intermediate when compared to the parental responses and no sex linkage was found. Backcross linkage analysis suggested that the same autosomal codominant gene controls both macrophage and B lymphocyte-LPS sensitivity.
已研究了脂多糖(LPS)对体外培养巨噬细胞的影响。LPS可触发巨噬细胞在体外产生淋巴细胞激活因子(LAF)和前列腺素E2(PGE2)。LPS对源自LPS敏感小鼠的巨噬细胞也具有细胞毒性,并会显著抑制其吞噬能力。LAF的产生和细胞毒性均归因于LPS对巨噬细胞的直接作用,且不需要淋巴细胞参与。在C3H/HeJ小鼠中,这些功能均异常。已确定了控制巨噬细胞对LPS这些反应的基因性质。与亲代反应相比,(C3H/HeJ×C3H/HeN)F1巨噬细胞的反应处于中间水平,且未发现性连锁。回交连锁分析表明,同一个常染色体共显性基因控制巨噬细胞和B淋巴细胞对LPS的敏感性。