首页> 美国卫生研究院文献>The Journal of Neuroscience >Astrocytes from Cerebral Cortex or Striatum Attract Adult Host Serotoninergic Axons into Intrastriatal Ventral Mesencephalic Co-Grafts
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Astrocytes from Cerebral Cortex or Striatum Attract Adult Host Serotoninergic Axons into Intrastriatal Ventral Mesencephalic Co-Grafts

机译:来自大脑皮层或纹状体的星形胶质细胞吸引成年宿主5-羟色胺能轴突进入纹状体腹侧中脑联合移植物中

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摘要

The identification of axon growth inhibitory molecules offers new hopes for repair of the injured CNS. However, the navigational ability of adult CNS axons and the guidance cues they can recognize are still essentially unknown. Astrocytes may express guidance molecules and are known to have different regional phenotypes. To evaluate their influence on the affinity of adult serotoninergic (5-HT) axons for a projection target, we co-implanted astrocytes from the neonatal striatum, cortex, or ventral mesencephalon together with fetal ventral mesencephalic tissue into the striatum of adult rats. Two months after surgery, quantification after in vitro5-[1,2-3H]serotonin ([3H]5-HT) uptake and autoradiography showed that ventral mesencephalic grafts with co-grafted cortical or striatal astrocytes were four times and three times, respectively, more densely innervated by host 5-HT axons than control ventral mesencephalic grafts with or without co-grafted ventral mesencephalic astrocytes. Immunohistochemistry for glial fibrillary acidic protein, vimentin, or chondroitin-sulfate proteoglycans revealed no qualitative or quantitative differences in host astroglial scar or production of inhibitory molecules that could explain these differences in 5-HT innervation. These results demonstrate that astrocytes grown in culture from different brain regions have the potential to influence the growth and maintenance of adult 5-HT axons in a graft of neural tissue from another brain region. It should now be feasible to identify the molecules expressed by cultured cortical or striatal, but not by ventral mesencephalic, astrocytes that have these tropic actions on 5-HT axons of the neostriatum.
机译:轴突生长抑制分子的鉴定为修复受损的中枢神经系统提供了新的希望。但是,成人中枢神经系统轴突的航行能力和他们可以识别的引导线索仍然是未知的。星形胶质细胞可以表达指导分子,并且已知具有不同的区域表型。为了评估它们对成年5-羟色胺能神经轴突(5-HT)轴突亲和力的影响,我们将来自新生儿纹状体,皮质或腹侧中脑的星形胶质细胞与胎儿腹侧中脑组织一起植入成年大鼠的纹状体中。手术后两个月,体外5- [1,2- 3 H] 5-羟色胺([ 3 H] 5-HT)摄取和放射自显影后的定量显示,腹侧中脑移植物与具有或不具有共移植的腹侧中脑星形胶质细胞的对照腹侧中脑移植相比,用共移植的皮质或纹状体星形胶质细胞分别较宿主腹侧中脑移植物更密集地受宿主5-HT轴突支配的四倍和三倍。胶质纤维酸性蛋白,波形蛋白或硫酸软骨素蛋白多糖的免疫组织化学显示,宿主星形胶质瘢痕中没有定性或定量的差异,也没有抑制分子产生的现象可以解释5-HT神经支配的这些差异。这些结果表明,来自不同大脑区域的培养物中生长的星形胶质细胞有可能影响来自另一个大脑区域的神经组织移植物中成年5-HT轴突的生长和维持。现在应该可以确定由培养的皮质或纹状体表达的分子,而不是由腹侧中脑星形胶质细胞表达的分子,这些分子对新纹状体的5-HT轴突具有这些嗜性作用。

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