Messias de Lima Cícero Fagner, Dos Santos Reis Maria Danielma, da Silva Ramos Fernando Wagner, Ayres-Martins Silvana, Smaniotto Salete
Laboratory of Cell Biology, Institute of Biology and Health Science, Federal University of Alagoas, Maceió, Alagoas, Brazil.
Cell Biol Int. 2017 May;41(5):577-584. doi: 10.1002/cbin.10747. Epub 2017 Mar 27.
The generation of new blood vessels is a complex process mediated by a variety of growth factors, and the growth hormone (GH) has been shown to act as a proangiogenic factor. In fact, human GH deficiency or excess are associated with endothelial dysfunction. Moreover, mouse models have revealed the action of GH in both tissue repair and in the microvascular circulation of normal tissues. In this study, we investigated the in vitro effects of GH on endothelial cells. Using a murine endothelioma cell line (tEnd.1), we demonstrated that GH has a mitogenic effect. The hormone also affected the endothelial cellular morphology and augmented the deposition of the extracellular matrix molecules, laminin, and fibronectin, on tEnd.1 surface. GH could stimulate tEnd.1 cell fugetaxis, in transwell chambers migration assay, and increased the formation of capillary-like structures in Matrigel®-coated plates. Given the important role of angiogenesis during tissue injury, for example, at ischemic lesions, these findings shed light on therapeutic angiogenesis, particularly in pathologies where the cardiovascular system has been compromised.
新血管的生成是一个由多种生长因子介导的复杂过程,生长激素(GH)已被证明是一种促血管生成因子。事实上,人类生长激素缺乏或过量与内皮功能障碍有关。此外,小鼠模型揭示了生长激素在组织修复和正常组织微血管循环中的作用。在本研究中,我们研究了生长激素对内皮细胞的体外影响。使用小鼠内皮瘤细胞系(tEnd.1),我们证明生长激素具有促有丝分裂作用。该激素还影响内皮细胞形态,并增加细胞外基质分子层粘连蛋白和纤连蛋白在tEnd.1表面的沉积。在Transwell小室迁移试验中,生长激素可刺激tEnd.1细胞趋化运动,并增加基质胶包被平板中毛细血管样结构的形成。鉴于血管生成在组织损伤(如缺血性病变)过程中的重要作用,这些发现为治疗性血管生成提供了思路,特别是在心血管系统受损的疾病中。