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唾液肽组蛋白-1可促进内皮细胞黏附、迁移和血管生成。

The salivary peptide histatin-1 promotes endothelial cell adhesion, migration, and angiogenesis.

作者信息

Torres Pedro, Díaz Jorge, Arce Maximiliano, Silva Patricio, Mendoza Pablo, Lois Pablo, Molina-Berríos Alfredo, Owen Gareth I, Palma Verónica, Torres Vicente A

机构信息

Institute for Research in Dental Sciences, Faculty of Dentistry, Universidad de Chile, Santiago, Chile.

Advanced Center for Chronic Diseases (ACCDiS), Universidad de Chile, Santiago, Chile.

出版信息

FASEB J. 2017 Nov;31(11):4946-4958. doi: 10.1096/fj.201700085R. Epub 2017 Jul 27.

Abstract

Saliva is a key factor that contributes to the high efficiency of wound healing in the oral mucosa. This is not only attributed to physical cues but also to the presence of specific peptides in the saliva, such as histatins. Histatin-1 is a 38 aa antimicrobial peptide, highly enriched in human saliva, which has been previously reported to promote the migration of oral keratinocytes and fibroblasts However, the participation of histatin-1 in other crucial events required for wound healing, such as angiogenesis, is unknown. Here we demonstrate that histatin-1 promotes angiogenesis, as shown , using the chick chorioallantoic membrane model, and by an tube formation assay, using both human primary cultured endothelial cells (HUVECs) and the EA.hy926 cell line. Specifically, histatin-1 promoted endothelial cell adhesion and spreading onto fibronectin, as well as endothelial cell migration in the wound closure and Boyden chamber assays. These actions required the activation of the Ras and Rab interactor 2 (RIN2)/Rab5/Rac1 signaling axis, as histatin-1 increased the recruitment of RIN2, a Rab5-guanine nucleotide exchange factor (GEF) to early endosomes, leading to sequential Rab5/Rac1 activation. Accordingly, interfering with either Rab5 or Rac1 activities prevented histatin-1-dependent endothelial cell migration. Finally, by immunodepletion assays, we showed that salivary histatin-1 is required for the promigratory effects of saliva on endothelial cells. In conclusion, we report that salivary histatin-1 is a novel proangiogenic factor that may contribute to oral wound healing.-Torres, P., Díaz, J., Arce, M., Silva, P., Mendoza, P., Lois, P., Molina-Berríos, A., Owen, G. I., Palma, V., Torres, V. A. The salivary peptide histatin-1 promotes endothelial cell adhesion, migration, and angiogenesis.

摘要

唾液是有助于口腔黏膜高效伤口愈合的关键因素。这不仅归因于物理线索,还归因于唾液中特定肽的存在,如组蛋白。组蛋白-1是一种38个氨基酸的抗菌肽,在人类唾液中高度富集,此前有报道称其可促进口腔角质形成细胞和成纤维细胞的迁移。然而,组蛋白-1在伤口愈合所需的其他关键事件(如血管生成)中的参与情况尚不清楚。在这里,我们证明组蛋白-1可促进血管生成,如使用鸡胚绒毛尿囊膜模型所示,以及通过使用人原代培养内皮细胞(HUVECs)和EA.hy926细胞系的管形成试验所示。具体而言,组蛋白-1促进内皮细胞在纤连蛋白上的黏附与铺展,以及在伤口闭合试验和博伊登室试验中的内皮细胞迁移。这些作用需要激活Ras和Rab相互作用蛋白2(RIN2)/Rab5/Rac1信号轴,因为组蛋白-1增加了RIN2(一种Rab5鸟嘌呤核苷酸交换因子(GEF))向早期内体的募集,导致Rab5/Rac1的顺序激活。因此,干扰Rab5或Rac1的活性可阻止组蛋白-1依赖的内皮细胞迁移。最后,通过免疫去除试验,我们表明唾液中的组蛋白-1是唾液对内皮细胞促迁移作用所必需的。总之,我们报告唾液组蛋白-1是一种新型促血管生成因子,可能有助于口腔伤口愈合。-托雷斯,P.,迪亚斯,J.,阿尔塞,M.,席尔瓦,P.,门多萨,P.,洛伊斯,P.,莫利纳-贝里奥斯,A.,欧文,G.I.,帕尔马,V.,托雷斯,V.A.唾液肽组蛋白-1促进内皮细胞黏附、迁移和血管生成。

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