Fan Yongfeng, Zhu Wei, Yang Michael, Zhu Yiqian, Shen Fanxia, Hao Qi, Young William L, Yang Guo-Yuan, Chen Yongmei
Center for Cerebrovascular Research, Department of Anesthesia and Perioperative Care, University of California San Francisco, 1001 Potrero Avenue, Room 3C-38, San Francisco, CA 94110, USA.
Brain Res. 2008 Jul 11;1219:1-7. doi: 10.1016/j.brainres.2008.05.003. Epub 2008 May 10.
Developmental endothelial locus-1 (Del-1) is a novel angiomatrix protein that has been shown to stimulate a potent angiogenic response and promote functional recovery in hind-limb and cardiac ischemia in animal models; however, its impact on cerebral angiogenesis is unknown. In this study, we investigated whether Del-1 overexpression via gene transfer induces cerebral angiogenesis in a murine model, and examined Del-1 expression after ischemic stroke. Cerebral Del-1 overexpression was achieved with AAV (adeno-associated virus) transduction system via stereotactic injection. Control mice were injected with AAV-lacZ. Del-1 gene transduction led to a significant induction of cerebral angiogenesis compared to AAV-lacZ treatment at 4 weeks after gene transfer (Del-1: 97+/-7 vs lacZ: 64+/-28, vessels/field, p<0.05). Mice transduced with AAV-Del-1 showed significantly elevated vascular densities for up to 6 weeks after gene delivery. In addition, double immunofluorescent staining showed co-localization of endothelial cell marker CD31 with BrdU (specific marker for proliferating cells), indicating that Del-1 promoted endogenous endothelial cell proliferation and angiogenesis. Our immunohistochemical staining also showed that Del-1 expression was markedly up-regulated in the peri-infarct area at 3 days after permanent focal cerebral ischemia compared to the sham-operated non-ischemic control. Our data suggest that Del-1 may participate in modulating cerebral angiogenesis, and that gene transfer of Del-1 may provide a novel and potent means for stimulating cerebral angiogenesis.
发育性内皮位点-1(Del-1)是一种新型血管基质蛋白,已被证明能在动物模型中刺激强烈的血管生成反应,并促进后肢和心脏缺血后的功能恢复;然而,其对脑内血管生成的影响尚不清楚。在本研究中,我们调查了通过基因转移过表达Del-1是否能在小鼠模型中诱导脑内血管生成,并检测了缺血性中风后Del-1的表达情况。通过立体定向注射利用腺相关病毒(AAV)转导系统实现脑内Del-1的过表达。对照小鼠注射AAV-lacZ。与基因转移后4周的AAV-lacZ处理相比,Del-1基因转导导致脑内血管生成显著增加(Del-1组:97±7,而lacZ组:64±28,血管数/视野,p<0.05)。用AAV-Del-1转导的小鼠在基因递送后长达6周显示血管密度显著升高。此外,双重免疫荧光染色显示内皮细胞标志物CD31与BrdU(增殖细胞特异性标志物)共定位,表明Del-1促进内源性内皮细胞增殖和血管生成。我们的免疫组织化学染色还显示,与假手术非缺血对照相比,永久性局灶性脑缺血后3天梗死周边区域的Del-1表达明显上调。我们的数据表明,Del-1可能参与调节脑内血管生成,并且Del-1的基因转移可能为刺激脑内血管生成提供一种新的有效手段。