Kermani Pouneh, Hempstead Barbara
Department of Medicine, Weill Medical College of Cornell University, 1300 York Avenue, NY, NY 10021, USA.
Trends Cardiovasc Med. 2007 May;17(4):140-3. doi: 10.1016/j.tcm.2007.03.002.
Recent studies indicate that, in addition to its neuropoietic actions, brain derived neurotrophic factor (BDNF) promotes endothelial cell survival and induces neoangiogenesis in ischemic tissues. Unlike many vascular growth factors that act on many vascular beds, BDNF activity is relatively restricted to central arteries, vessels of cardiac and skeletal muscle, and skin. Studies of newly described biologic mediators that act on large-vessel and microvascular beds in these organs will help us to better understand organ-specific vascular development, as well as to develop novel therapeutic strategies to improve the condition of patients with cardiac and peripheral vascular disease. In this review, we summarize dual proangiogenic actions of BDNF, which, through local activation of TrkB receptor, expressed on a subpopulation of endothelial cells and, in addition, by recruitment of bone marrow-derived cells, contribute to neoangiogenesis.
最近的研究表明,脑源性神经营养因子(BDNF)除了具有神经生成作用外,还能促进内皮细胞存活,并在缺血组织中诱导新血管生成。与许多作用于多个血管床的血管生长因子不同,BDNF的活性相对局限于中枢动脉、心脏和骨骼肌的血管以及皮肤。对这些器官中作用于大血管和微血管床的新发现生物介质的研究,将有助于我们更好地理解器官特异性血管发育,并开发新的治疗策略以改善心脏和外周血管疾病患者的病情。在这篇综述中,我们总结了BDNF的双重促血管生成作用,即通过局部激活在内皮细胞亚群上表达的TrkB受体,以及此外通过募集骨髓来源的细胞,促进新血管生成。