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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Angiogenic and astroglial responses to vascular endothelial growth factor administration in adult rat brain.
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Angiogenic and astroglial responses to vascular endothelial growth factor administration in adult rat brain.

机译:成年大鼠大脑对血管内皮生长因子给药的血管生成和星形胶质细胞反应。

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The effects of exogenous vascular endothelial growth factor (VEGF) on angiogenesis, blood-brain barrier permeability and astroglial proliferation in the adult rat CNS in situ were investigated. Recombinant human VEGF(165) (25 or 50 ng/ml) was delivered for up to 1 week using either intracerebral osmotic minipumps or less traumatic subdural gelatin sponge placement. By 3 days, VEGF delivery caused significantly increased cerebral angiogenesis (25 ng/ml was most effective) in both experimental models when compared to saline controls; VEGF infusion resulted in a 100% increase in an index of vascular proliferation, and gelatin sponge delivery produced a 65% increase. The blood-brain barrier hallmark endothelial glucose transporter-1 was not present in nascent vascular sprouts. Infusion of VEGF produced extensive protein leakage that persisted after saline-induced permeability was mostly resolved, while gelatin sponge administration caused milder barrier dysfunction. Administration of the angiogenic factor had unexpected proliferative effects on astroglia in both models, resulting in an 80-85% increase in mitotically active astroglia when compared to controls. Immunohistochemical results and semi-quantitative reverse transcriptase-polymerase chain reaction indicated that the VEGF receptors flk-1 and flt-1 were up-regulated in response to the infusion trauma; flt-1 was localized to reactive astroglia, while flk-1 was expressed in vascular endothelium but predominantly in neuronal somata and processes adjacent to the delivery site. mRNA for the VEGF(121), VEGF(165) and VEGF(188) isoforms was also increased after delivery of the recombinant protein.These data show that VEGF application has substantial proliferative effects on CNS endothelium and astroglia and causes up-regulation of its own message. Flt-1 and flk-1 receptor mRNAs and proteins are up-regulated in both vascular and non-vascular cell types following infusion trauma. From these results we suggest that administered VEGF has heretofore unanticipated pleiotrophic effects in the adult CNS.
机译:研究了外源性血管内皮生长因子(VEGF)对成年大鼠中枢神经系统原位血管生成,血脑屏障通透性和星形胶质细胞增殖的影响。重组人VEGF(165)(25或50 ng / ml)可以使用脑内渗透微型泵或创伤较小的硬膜下明胶海绵放置长达1周。到3天时,与盐水对照组相比,在两个实验模型中,VEGF递送均导致脑血管生成显着增加(25 ng / ml最有效)。 VEGF输注导致血管增殖指数增加了100%,明胶海绵的输送增加了65%。新生血管芽中不存在血脑屏障标志性内皮葡萄糖转运蛋白-1。输注VEGF会产生大量蛋白渗漏,并在盐水诱导的通透性基本消除后持续存在,而使用明胶海绵则引起较轻的屏障功能障碍。在两个模型中,血管生成因子的给药均对星形胶质细胞具有出乎意料的增殖作用,与对照组相比,有丝分裂活性星形胶质细胞增加80-85%。免疫组织化学结果和半定量逆转录聚合酶链反应表明,VEGF受体flk-1和flt-1响应输注创伤而被上调。 flt-1定位于反应性星形胶质细胞,而flk-1在血管内皮中表达,但主要在神经元的躯体和靠近递送部位的过程中表达。重组蛋白递送后,VEGF(121),VEGF(165)和VEGF(188)亚型的mRNA也增加了。这些数据表明VEGF的应用对CNS内皮和星形胶质细胞具有实质性增生作用,并导致其上调。自己的信息。输注创伤后,在血管和非血管细胞类型中,Flt-1和flk-1受体的mRNA和蛋白均上调。根据这些结果,我们提示,在成人中枢神经系统中,施用的VEGF迄今为止具有无法预料的多营养作用。

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