Tilly B C, Tertoolen L G, Remorie R, Ladoux A, Verlaan I, de Laat S W, Moolenaar W H
Hubrecht Laboratory, Netherlands Institute for Developmental Biology, Utrecht.
J Cell Biol. 1990 Apr;110(4):1211-5. doi: 10.1083/jcb.110.4.1211.
Histamine receptors are present on the surface of various normal and tumor-derived cell types, where their biological function is incompletely understood. Here we report that histamine not only stimulates cell proliferation under serum-free conditions, but also is chemotactic for human carcinoma (Hela and A431) and melanoma (A875) cells expressing H1 type receptors. Histamine was found to be a potent activator of phospholipase C, leading to polyphosphoinositide hydrolysis and subsequent intracellular Ca2+ mobilization. In addition, histamine also causes the protein kinase C-mediated activation of Na+/H+ exchange, as evidenced by an amiloride-sensitive rise in cytoplasmic pH. All histamine-induced responses, including chemotaxis and DNA synthesis, are completely inhibited by the H1 receptor antagonist pyrilamine, but not by cimetidine, an inhibitor of histamine H2 type receptors. Our results suggest that histamine may have a previously unrecognized role in the migration and proliferation of cells expressing H1 receptors.
组胺受体存在于各种正常细胞和肿瘤衍生细胞类型的表面,但其生物学功能尚未完全明确。在此我们报告,组胺不仅在无血清条件下刺激细胞增殖,而且对表达H1型受体的人癌细胞(Hela和A431)和黑色素瘤细胞(A875)具有趋化作用。研究发现组胺是磷脂酶C的有效激活剂,可导致多磷酸肌醇水解及随后的细胞内Ca2+动员。此外,组胺还引起蛋白激酶C介导的Na+/H+交换激活,胞质pH值的阿米洛利敏感升高证明了这一点。所有组胺诱导的反应,包括趋化作用和DNA合成,均被H1受体拮抗剂吡苄明完全抑制,但不受组胺H2型受体抑制剂西咪替丁的抑制。我们的结果表明,组胺可能在表达H1受体的细胞迁移和增殖中具有先前未被认识到的作用。