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首页> 外文期刊>Glia >Astrocytic endogenous glial cell derived neurotrophic factor production is enhanced by bone marrow stromal cell transplantation in the ischemic boundary zone after stroke in adult rats
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Astrocytic endogenous glial cell derived neurotrophic factor production is enhanced by bone marrow stromal cell transplantation in the ischemic boundary zone after stroke in adult rats

机译:成年大鼠中风后缺血边界区域的骨髓基质细胞移植可增强星形胶质细胞内源性神经胶质细胞源性神经营养因子的产生

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Bone marrow stromal cells (BMSCs) facilitate functional recovery in rats after focal ischemic attack. Growing evidence suggests that the secretion of various bioactive factors underlies BMSCs' beneficial effects. This study investigates the expression of glial cell derived neurotrophic factor (GDNF) in the ischemic hemisphere with or without BMSC administration. Adult male Wistar rats were subjected to 2 h of middle cerebral artery occlusion followed by an injection of 3 × 10~6 BMSCs (n = 11) or phosphate-buffered saline (n = 10) into the tail vein 24 h later. Animals were sacrificed seven days later. Single and double immunohistochemical staining was performed to measure GDNF, Ki67, doublecortin, and glial fibrillary acidic protein expression as well as the number of apoptotic cells along the ischemic boundary zone (IBZ) and/or in the subventricular zone (SVZ). BMSC treatment significantly increased GDNF expression and decreased the number of apoptotic cells in the IBZ (P < 0.05). GDNF expression was colocalized with GFAP. Meanwhile, BMSCs increased the number of Ki-67 positive cells and the density of DCX positive migrating neuroblasts (P < 0.05). GDNF expression was significantly increased in single astrocytes collected from animals treated with BMSCs, and in astrocytes cocultured with BMSCs after OGD (P < 0.05). Our data suggest that BMSCs increase GDNF levels in the ischemic hemisphere; the major source of GDNF protein is reactive astrocytes. We propose that the increase of GDNF in response to BMSC administration creates a hospitable environment for local cellular repair as well as for migrating neuroblasts from the SVZ, and thus contributes to the functional improvement.
机译:局灶性脑缺血发作后,骨髓基质细胞(BMSC)促进大鼠功能恢复。越来越多的证据表明,各种生物活性因子的分泌是BMSC有益作用的基础。这项研究调查了神经胶质细胞源性神经营养因子(GDNF)在缺血半球中是否使用BMSC的表达。成年雄性Wistar大鼠在大脑中部动脉闭塞2小时后,在24小时后向尾静脉注射3×10〜6 BMSC(n = 11)或磷酸盐缓冲盐水(n = 10)。 7天后处死动物。进行了单次和两次免疫组化染色以测量GDNF,Ki67,双皮质素和神经胶质原纤维酸性蛋白的表达,以及沿缺血边界区(IBZ)和/或脑室下区(SVZ)的凋亡细胞数。 BMSC处理可显着增加GDNF的表达,并减少IBZ中凋亡细胞的数量(P <0.05)。 GDNF表达与GFAP共定位。同时,BMSCs增加了Ki-67阳性细胞的数量和DCX阳性迁移成神经细胞的密度(P <0.05)。 OGD后,从用BMSCs处理的动物收集的单个星形胶质细胞和与BMSCs共培养的星形胶质细胞中GDNF表达显着增加(P <0.05)。我们的数据表明,骨髓间充质干细胞会增加缺血性半球的GDNF水平。 GDNF蛋白的主要来源是反应性星形胶质细胞。我们建议响应BMSC管理GDNF的增加为本地细胞修复以及从SVZ迁移成神经细胞创造了一个好客的环境,因此有助于功能改善。

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