Weinstein S L, June C H, DeFranco A L
Department of Physiology, University of California, San Francisco 94143.
J Immunol. 1993 Oct 1;151(7):3829-38.
Induced protein tyrosine phosphorylation is an early intracellular event in LPS-stimulated murine macrophages that appears to play a role in signal transduction. We have now demonstrated that LPS also increases protein tyrosine phosphorylation in human monocyte-derived macrophages and in the human monocytic cell line, THP-1. This response was rapidly elicited by biologically active forms of LPS or lipid A, at concentrations of these bacterial components that stimulate anti-bacterial responses by human macrophages. Inhibition of the LPS-induced tyrosine phosphorylation response with the tyrosine kinase inhibitor, herbimycin A, was accompanied by the inhibition of the secretion of TNF-alpha by human macrophages. These results extend previous work with murine macrophages and provide further support for the hypothesis that induced protein tyrosine phosphorylation is an important signaling reaction in macrophages after LPS exposure. In addition, CD14, which is thought to be a receptor for LPS, appeared to mediate the induced phosphorylation response in human macrophages and THP-1 cells at low LPS concentrations. Two antibodies against CD14, 3C10 and 60b, which have been shown to prevent LPS binding to CD14, specifically inhibited the protein tyrosine phosphorylation induced by nanogram per milliliter concentrations of LPS in these cells. The antibody-mediated inhibition did not appear to involve engagement of surface FcR because a preparation of F(ab')2/Fab fragments of the 60b antibody also prevented LPS-induced tyrosine phosphorylation. At higher concentrations of LPS (> or = 10 ng/ml), however, anti-CD14 antibodies did not prevent the induction of protein tyrosine phosphorylation, suggesting that a lower affinity CD14-independent pathway also mediates the tyrosine phosphorylation response. Because CD14-dependent and CD14-independent recognition of LPS appear to lead to the same functional responses by macrophages, induced protein tyrosine phosphorylation may be part of a shared intracellular signaling pathway.
诱导的蛋白酪氨酸磷酸化是脂多糖(LPS)刺激的小鼠巨噬细胞中的一种早期细胞内事件,似乎在信号转导中起作用。我们现已证明,LPS也会增加人单核细胞衍生的巨噬细胞以及人单核细胞系THP-1中的蛋白酪氨酸磷酸化。这种反应可由生物活性形式的LPS或脂多糖A迅速引发,这些细菌成分的浓度能刺激人巨噬细胞产生抗菌反应。用酪氨酸激酶抑制剂赫曲霉素A抑制LPS诱导的酪氨酸磷酸化反应,同时会抑制人巨噬细胞分泌肿瘤坏死因子-α(TNF-α)。这些结果扩展了先前对小鼠巨噬细胞的研究工作,并为以下假说提供了进一步支持:诱导的蛋白酪氨酸磷酸化是LPS暴露后巨噬细胞中一种重要的信号反应。此外,被认为是LPS受体的CD14,在低LPS浓度下似乎介导了人巨噬细胞和THP-1细胞中的诱导磷酸化反应。两种针对CD14的抗体3C10和60b已被证明可阻止LPS与CD14结合,它们能特异性抑制这些细胞中每毫升纳克浓度的LPS诱导的蛋白酪氨酸磷酸化。抗体介导的抑制似乎不涉及表面FcR的结合,因为60b抗体的F(ab')2/Fab片段制剂也能阻止LPS诱导的酪氨酸磷酸化。然而,在较高浓度的LPS(≥10 ng/ml)下,抗CD14抗体并不能阻止蛋白酪氨酸磷酸化的诱导,这表明一种低亲和力的不依赖CD14的途径也介导了酪氨酸磷酸化反应。由于LPS的CD14依赖性和CD14非依赖性识别似乎会导致巨噬细胞产生相同的功能反应,诱导的蛋白酪氨酸磷酸化可能是共享细胞内信号通路的一部分。