Ho Hoai-Ky V, Jang James J, Kaji Shuichiro, Spektor Gary, Fong Annie, Yang Phillip, Hu Bob S, Schatzman Randy, Quertermous Thomas, Cooke John P
Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, Calif, USA.
Circulation. 2004 Mar 16;109(10):1314-9. doi: 10.1161/01.CIR.0000118465.36018.2D. Epub 2004 Feb 23.
Developmentally regulated endothelial locus-1 (Del-1) is an extracellular matrix protein that is expressed by endothelial cells during embryological vascular development. We speculated that Del-1 may be reexpressed in ischemia and may be involved in endogenous angiogenesis.
Del-1 protein was detected by immunohistochemistry in murine ischemic hindlimb after femoral artery excision. To determine whether exogenous Del-1 would augment angiogenesis in vivo, Del-1 or vehicle was administered for 3 weeks by intramuscular injection of murine ischemic hindlimbs. Angiogenesis was quantified by gadolinium-MRI perfusion and capillary densitometry. We used a disc angiogenesis system (DAS) to characterize the angiogenic response to vehicle (PBS), Del-1, Del-1 mutant (altered RGD domain), Del-1 minor (truncated discoidin-I-like domain), or basic fibroblast growth factor. After 14 days, the discs were extracted and sectioned to quantify vascular growth by morphometry. Endogenous Del-1 protein expression was increased in ischemic hindlimbs. Administration of Del-1 increased hindlimb vascular flow index and capillary density. In the DAS, Del-1 doubled fibrovascular growth, as did basic fibroblast growth factor. However, angiogenesis was not enhanced by the Del-1 mutant or Del-1 minor proteins.
Del-1 is expressed in ischemic tissue. Del-1 stimulates angiogenesis, an effect that is dependent on the RGD motif and a second signaling sequence in the discoidin-I-like domain. Exogenous intramuscular administration of Del-1 significantly enhances angiogenesis in the murine ischemic hindlimb. Del-1 may prove to be a novel therapeutic agent for patients with ischemia.
发育调控性内皮位点-1(Del-1)是一种细胞外基质蛋白,在胚胎血管发育过程中由内皮细胞表达。我们推测Del-1可能在缺血时重新表达,并可能参与内源性血管生成。
通过免疫组织化学检测股动脉切除术后小鼠缺血后肢中的Del-1蛋白。为了确定外源性Del-1是否会增强体内血管生成,通过肌肉注射对小鼠缺血后肢给予Del-1或赋形剂,持续3周。通过钆增强磁共振成像灌注和毛细血管密度测定法对血管生成进行定量。我们使用圆盘血管生成系统(DAS)来表征对赋形剂(PBS)、Del-1、Del-1突变体(RGD结构域改变)、Del-1小片段(截短的盘状结构域I样结构域)或碱性成纤维细胞生长因子的血管生成反应。14天后,取出圆盘并切片,通过形态计量学对血管生长进行定量。缺血后肢中内源性Del-1蛋白表达增加。给予Del-1可增加后肢血管流量指数和毛细血管密度。在DAS中,Del-1使纤维血管生长增加一倍,碱性成纤维细胞生长因子也有同样效果。然而,Del-1突变体或Del-1小片段蛋白并未增强血管生成。
Del-1在缺血组织中表达。Del-1刺激血管生成,这种作用依赖于RGD基序和盘状结构域I样结构域中的第二个信号序列。外源性肌肉注射Del-1可显著增强小鼠缺血后肢的血管生成。Del-1可能被证明是缺血患者的一种新型治疗药物。