Springer M L, Chen A S, Kraft P E, Bednarski M, Blau H M
Department of Molecular Pharmacology, Stanford University School of Medicine, CA 94305-5332, USA.
Mol Cell. 1998 Nov;2(5):549-58. doi: 10.1016/s1097-2765(00)80154-9.
Constitutive expression of VEGF after implantation of genetically engineered myoblasts into non-ischemic muscle led to an increase in vascular structures. Previously, effects of VEGF delivery to adult muscle have only been reported in ischemic tissues. The resulting vascular structures were reminiscent of those formed during embryonic vasculogenesis, rather than angiogenesis, sprouting from preexisting vessels. Initially, VEGF caused an accumulation of endothelial cells and macrophages, followed by networks of vascular channels and hemangiomas with locally high serum VEGF levels. No effects were evident in adjacent tissue or contralateral legs, where low serum VEGF was detected. These data suggest that the induction by VEGF of angiogenesis or vasculogenesis may be dose-dependent. Furthermore, VEGF expression must be carefully modulated, as overexpression is deleterious.
将基因工程化的成肌细胞植入非缺血性肌肉后,血管内皮生长因子(VEGF)的组成型表达导致血管结构增加。此前,VEGF递送至成年肌肉的作用仅在缺血组织中有报道。所形成的血管结构让人联想到胚胎血管生成过程中形成的结构,而非从现有血管中萌芽的血管生成。最初,VEGF导致内皮细胞和巨噬细胞积聚,随后是血管通道网络和血清VEGF水平局部升高的血管瘤。在检测到低血清VEGF的相邻组织或对侧腿部未观察到明显影响。这些数据表明,VEGF对血管生成或血管发生的诱导可能是剂量依赖性的。此外,由于VEGF过表达有害,其表达必须得到谨慎调控。