Pejler Gunnar, Knight Stefan D, Henningsson Frida, Wernersson Sara
Swedish University of Agricultural Sciences, Dept of Anatomy, Physiology and Biochemistry, Uppsala 75123, Sweden.
Trends Immunol. 2009 Aug;30(8):401-8. doi: 10.1016/j.it.2009.04.008. Epub 2009 Jul 28.
When mast cells are activated they can respond by releasing their secretory granule compounds, including mast cell-specific proteases of chymase, tryptase and carboxypeptidase A (MC-CPA) type. MC-CPA is a dominant protein component of the mast cell granule and the MC-CPA gene is extremely highly expressed. Despite this, relatively little has been known of its biological function. However, the recent generation of mouse strains lacking MC-CPA has opened up new possibilities for investigations related to this protease. This recent development has revealed a role for MC-CPA in regulating innate immunity responses, including the degradation of harmful substances such as the vasoconstrictive factor endothelin 1 and snake venom toxins. Here, we summarize the current knowledge of MC-CPA.
肥大细胞被激活后,可通过释放其分泌颗粒化合物做出反应,这些化合物包括肥大细胞特异性蛋白酶,如糜蛋白酶、组织蛋白酶G和羧肽酶A(MC-CPA)类型。MC-CPA是肥大细胞颗粒的主要蛋白质成分,且MC-CPA基因表达极高。尽管如此,人们对其生物学功能的了解相对较少。然而,最近培育出的缺乏MC-CPA的小鼠品系为与这种蛋白酶相关的研究开辟了新的可能性。这一最新进展揭示了MC-CPA在调节固有免疫反应中的作用,包括降解诸如血管收缩因子内皮素1和蛇毒毒素等有害物质。在此,我们总结了目前关于MC-CPA的知识。