Nast C C, LeDuc L E
Department of Pathology, Harbor-UCLA Medical Center, Torrance 90509.
Dig Dis Sci. 1988 Mar;33(3 Suppl):50S-57S. doi: 10.1007/BF01538131.
An important component of host defenses is the ability of inflammatory cells to detect and respond to minute concentrations of chemoattractant substances. Chemotactic peptides elaborated by both bacteria and leukocytes are the focus of this review. These peptides induce directed migration of inflammatory cells towards their targets, and stimulate biological functions including degranulation, release of oxygen radicals, phagocytosis, and eicosanoid production. Among the released eicosanoids, leukotriene B4 potentiates the leukocyte response. As with other chemotactic factors, these functions are regulated partially through differential coupling to high- and low-affinity receptors and via calcium as the second messenger. Some chemotactic peptides are elaborated by normal colonic luminal bacteria. Recent evidence demonstrates that these peptides can produce mucosal inflammation in vivo. A possible mechanism for this effect involves abnormal colonic permeability in susceptible individuals that allows bacterial chemotactic peptides access to the mucosa where they may induce inflammation. Remaining questions include the mechanism by which the mucosal barrier is breached and the role of leukotrienes in the potentiation of colonic inflammation.
宿主防御的一个重要组成部分是炎症细胞检测并对微量趋化物质作出反应的能力。细菌和白细胞产生的趋化肽是本综述的重点。这些肽诱导炎症细胞向其靶标进行定向迁移,并刺激包括脱颗粒、氧自由基释放、吞噬作用和类花生酸生成在内的生物学功能。在释放的类花生酸中,白三烯B4增强白细胞反应。与其他趋化因子一样,这些功能部分通过与高亲和力和低亲和力受体的差异偶联以及以钙作为第二信使来调节。一些趋化肽由正常结肠腔细菌产生。最近的证据表明,这些肽可在体内引起黏膜炎症。这种效应的一种可能机制涉及易感个体结肠通透性异常,使细菌趋化肽能够进入黏膜,在那里它们可能诱发炎症。尚待解决的问题包括黏膜屏障被破坏的机制以及白三烯在结肠炎症增强中的作用。