Castillo-Briceño Patricia, Sepulcre María P, Chaves-Pozo Elena, Meseguer José, García-Ayala Alfonsa, Mulero Victoriano
Department of Cell Biology and Histology, Faculty of Biology, University of Murcia, 30100 Murcia, Spain.
Mol Immunol. 2009 Apr;46(7):1409-15. doi: 10.1016/j.molimm.2008.12.005. Epub 2009 Jan 29.
The innate immune system mediates the initial inflammatory response that follows infection or injury. Although the innate immune response of fish to infection has been relatively well characterized during recent years at both cellular and molecular levels, no studies have examined the role of extracellular matrix (ECM) in the regulation of innate immunity and inflammation. We report here that collagen and gelatin in vitro were able to prime the respiratory burst of phagocytes from the bony fish gilthead seabream. In addition, collagen and gelatin induced a specific set of immune-related and ECM remodelling enzymes that substantially differed from that induced by pathogen-associated molecular patterns. Notably, both collagen and gelatin induced the expression of interleukin-1beta, chemokine (C-C motif) ligand 4 and matrix metalopeptidases (MMP) 9 and 13 in acidophilic granulocytes and macrophages but were unable to significantly increase the expression of other pro-inflammatory genes. Furthermore, it was found that the MMP2/MMP9 inhibitor V had a dose-dependent inhibitory effect on seabream phagocyte activation by either collagen or gelatin. In contrast, pre-treatment of collagen and gelatin by collagenase resulted in a higher stimulatory capacity compared to non-digested proteins. Collectively, these results indicate that collagen fragments produced by the action of different host proteases, and probably released by infectious agents, are sensed by fish phagocytes. Therefore, we propose that, besides to the well-established response to infection, the innate immune system of fish is able to respond to tissue injury.
先天性免疫系统介导感染或损伤后的初始炎症反应。尽管近年来鱼类对感染的先天性免疫反应在细胞和分子水平上已得到相对充分的表征,但尚无研究探讨细胞外基质(ECM)在先天性免疫和炎症调节中的作用。我们在此报告,体外的胶原蛋白和明胶能够引发硬骨鱼金头鲷吞噬细胞的呼吸爆发。此外,胶原蛋白和明胶诱导了一组特定的免疫相关和ECM重塑酶,这与病原体相关分子模式诱导的酶有很大不同。值得注意的是,胶原蛋白和明胶均诱导嗜酸性粒细胞和巨噬细胞中白细胞介素-1β、趋化因子(C-C基序)配体4以及基质金属肽酶(MMP)9和13的表达,但无法显著增加其他促炎基因的表达。此外,发现MMP2/MMP9抑制剂V对胶原蛋白或明胶激活的金头鲷吞噬细胞具有剂量依赖性抑制作用。相反,与未消化的蛋白质相比,用胶原酶预处理胶原蛋白和明胶会产生更高的刺激能力。总体而言,这些结果表明,由不同宿主蛋白酶作用产生且可能由感染因子释放的胶原蛋白片段可被鱼类吞噬细胞感知。因此,我们提出,除了对感染的既定反应外,鱼类的先天性免疫系统还能够对组织损伤做出反应。