Gianni-Barrera Roberto, Bartolomeo Mariateresa, Vollmar Brigitte, Djonov Valentin, Banfi Andrea
*Cell and Gene Therapy, Department of Biomedicine, University of Basel, and Department of Surgery, Basel University Hospital, Hebelstrasse 20, CH-4031 Basel, Switzerland.
†Institute for Experimental Surgery, Rostock University Medical Center, Schillingallee, D-18057 Rostock, Germany.
Biochem Soc Trans. 2014 Dec;42(6):1637-42. doi: 10.1042/BST20140234.
Therapeutic angiogenesis is an attractive strategy to treat patients suffering from ischaemic conditions and vascular endothelial growth factor-A (VEGF) is the master regulator of blood vessel growth. However, VEGF can induce either normal or aberrant angiogenesis depending on its dose localized in the microenvironment around each producing cell in vivo and on the balanced stimulation of platelet-derived growth factor-BB (PDGF-BB) signalling, responsible for pericyte recruitment. At the doses required to induce therapeutic benefit, VEGF causes new vascular growth essentially without sprouting, but rather through the alternative process of intussusception, or vascular splitting. In the present article, we briefly review the therapeutic implications of controlling VEGF dose on one hand and pericyte recruitment on the other, as well as the key features of intussusceptive angiogenesis and its regulation.
治疗性血管生成是治疗缺血性疾病患者的一种有吸引力的策略,血管内皮生长因子-A(VEGF)是血管生长的主要调节因子。然而,VEGF可诱导正常或异常血管生成,这取决于其在体内每个产生细胞周围微环境中的剂量,以及对负责周细胞募集的血小板衍生生长因子-BB(PDGF-BB)信号的平衡刺激。在诱导治疗益处所需的剂量下,VEGF主要通过套叠或血管分裂这一替代过程而非发芽来引起新血管生长。在本文中,我们一方面简要回顾控制VEGF剂量和另一方面周细胞募集的治疗意义,以及套叠式血管生成的关键特征及其调节。