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胶质细胞对中枢神经系统神经元存活、突起生长和再生的支持作用。

Glial support of CNS neuronal survival, neurite growth and regeneration.

机构信息

Molecular Neurobiology Laboratory, Department of Neurology, University of Düsseldorf, Düsseldorf (F.R.G.).

出版信息

Restor Neurol Neurosci. 1991 Jan 1;2(4):229-32. doi: 10.3233/RNN-1991-245610.

Abstract

In an attempt to identify specific molecular and cellular requirements necessary to support long-term maintenance and differentiation of central neurons we have identified laminin-HSPG and free fibronectin as two major neurite promoting substrate adhesion factors released by immature cerebral astrocytes in serum-free culture. Astrocytes further secrete diffusible neurotrophic protein factor(s) which are permanently required for survival of cultured neurons from various brain regions. However, both the presence of substrate-bound neurite-promoting factors and diffusible neurotrophic activities were not sufficient to support long-term maintenance of central neurons in culture. Cell contact-mediated interactions which appear to be cell type-restricted (e.g. to neurons and astrocytes, but not to fibroblasts) are further required for neuronal stabilization. The implantation of immature astroglial cells into the injured adult CNS should provide a supportive environmental condition for damaged neurons to enhance their recovery and stimulate regenerative responses.

摘要

为了确定支持中枢神经元长期维持和分化所必需的特定分子和细胞要求,我们已经鉴定出层粘连蛋白-HSPG 和游离纤维连接蛋白,它们是无血清培养的未成熟大脑星形胶质细胞释放的两种主要促进神经突生长的基质粘附因子。星形胶质细胞进一步分泌扩散性神经营养蛋白因子,这些因子对于来自不同脑区的培养神经元的存活是永久性需要的。然而,基质结合的神经突促进因子和扩散性神经营养活性的存在不足以支持中枢神经元在培养中长期维持。细胞接触介导的相互作用似乎是细胞类型特异性的(例如,仅限于神经元和星形胶质细胞,但不限于成纤维细胞),对于神经元的稳定化是进一步需要的。将未成熟的星形胶质细胞植入受伤的成年中枢神经系统应该为受损神经元提供支持性环境条件,以增强它们的恢复并刺激再生反应。

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