Jararhagin disruption of endothelial cell anchorage is enhanced in collagen enriched matrices. (15th December 2015)

• Record Type: Journal Article
• Authors: Baldo, C.; Lopes, D.S.; Faquim-Mauro, E.L.; Jacysyn, J.F.; Niland, S.; Eble, J.A.; Clissa, P.B.; Moura-da-Silva, A.M.
• Is Part Of: Toxicon. Volume 108(2015)
• Page Start: 240
• Page End: 248
• Publication Date: 2015-12-15
• Subjects: Snake venom -- Metalloproteinase -- Endothelial cell -- Extracellular matrix -- Hemorrhage -- Collagen; Toxins -- Periodicals; Venom -- Periodicals; 615.9
• DOI: 10.1016/j.toxicon.2015.10.016
• Languages: English
• ISSNs: 0041-0101

Abstract

Abstract: Hemorrhage is one of the most striking effects of bites by viper snakes resulting in fast bleeding and ischemia in affected tissues. Snake venom metalloproteinases (SVMPs) are responsible for hemorrhagic activity, but the mechanisms involved in SVMP-induced hemorrhage are not entirely understood and the study of such mechanisms greatly depends on in vivo experiments. In vivo, hemorrhagic SVMPs accumulate on basement membrane (BM) of venules and capillary vessels allowing the hydrolysis of collagen IV with consequent weakness and rupture of capillary walls. These effects are not reproducible in vitro with conventional endothelial cell cultures. In this study we used two-dimension (2D) or three-dimension (3D) cultures of HUVECs on matrigel and observed the same characteristics as in ex vivo experiments: only the hemorrhagic toxin was able to localize on surfaces or internalize endothelial cells in 2D cultures or in the surface of tubules formed on 3D cultures. The contribution of matrigel, fibronectin and collagen matrices in jararhagin-induced endothelial cell damage was then analyzed. Collagen and matrigel substrates enhanced the endothelial cell damage induced by jararhagin allowing toxin binding to focal adhesions, disruption of stress fibers, detachment and apoptosis. The higher affinity of jararhagin to collagen than to fibronectin explains the localization of the toxin within BM. Moreover, once located in BM, interactions of jararhagin with α2 β1 integrin would favor its localization on focal adhesions, as observed in our study. The accumulation of toxin in focal adhesions, observed only in cells grown in collagen matrices, would explain the enhancement of cell damage in these matrices and reflects the actual interaction among toxin, endothelial cells and BM components that occurs in vivo and results in the hemorrhagic lesions induced by viper venoms. Highlights: 2D/3D-cultures of HUVECs are good models to study the disruption of capillary vessels related to venom-induced hemorrhage. In collagen matrices, jararhagin co-localizes with focal adhesions of endothelial cells. Jararhagin accumulation in focal adhesions was associated to binding to collagen and α2β1 integrin. Collagen and matrigel substrates enhanced the endothelial cell detachment and apoptosis induced by jararhagin.