Abstract
Integrin avβ3 is most likely the foremost modulator of angiogenesis among all known integrins. Recombinant disintegrin DisBa-01, originally obtained from snake venom glands, binds to avβ3, thereby significantly inhibiting adhesion and generating in vivo anti-metastatic ability. However, its function in mediator production is not clear. Here, we observed that the mediators VEGF-A, IL-8, and TGF-β are not produced by human umbilical vein endothelial cells (HUVEC cell line) or monocyte/macrophage cells (SC cell line) when cells adhered to vitronectin. However, when exposed to DisBa-01, HUVECs produced higher levels of TGF-β, and SC cells produced higher levels of VEGF-A. Nonetheless, HUVECs also showed an enhancement of apoptosis after losing adherence when exposed to disintegrin, which is a characteristic of anoikis. We propose that disintegrin DisBa-01 could be used to modulate integrin avβ3 functions. © 2014 Landes Bioscience.
Author supplied keywords
Cite
CITATION STYLE
Ribeiro, L. C. A., Massimino, L. C., Durante, A. C., Tansini, A., Urbaczek, A. C., Selistre-de-Araújo, H. S., & Carlos, I. Z. (2014). Recombinant disintegrin targets a(v) β(3) integrin and leads to mediator production. Cell Adhesion and Migration, 8(1), 60–65. https://doi.org/10.4161/cam.27698
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.