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环磷酸腺苷(cAMP)水平升高足以在体外促进脊髓运动神经元的存活。

Cyclic AMP elevation is sufficient to promote the survival of spinal motor neurons in vitro.

作者信息

Hanson M G, Shen S, Wiemelt A P, McMorris F A, Barres B A

机构信息

Stanford University School of Medicine, Department of Neurobiology, Stanford, California 94305-5125, USA.

出版信息

J Neurosci. 1998 Sep 15;18(18):7361-71. doi: 10.1523/JNEUROSCI.18-18-07361.1998.

Abstract

The short-term survival of highly purified embryonic spinal motor neurons (SMNs) in culture can be promoted by many peptide trophic factors, including brain-derived neurotrophic factor (BDNF), ciliary neurotrophic factor (CNTF), fibroblast growth factor (FGF), glial-derived neurotrophic factor (GDNF), and hepatocyte growth factor (HGF). We have asked whether these peptides are sufficient to promote the long-term survival of purified E15 SMNs. Contrary to previous reports, we find that when SMNs are cultured in serum-free medium containing a single peptide trophic factor only approximately one-third of the cells survive for 3 d in culture. When multiple factors are combined, additive effects on survival are observed transiently, but by 7 d of culture the majority of SMNs has died. Surprisingly, when cAMP levels are elevated, the majority of SMNs extend processes and survive for 1 week in culture in the absence of peptide trophic factors, even in low-density cultures. A combination of five peptide trophic factors, together with cAMP elevation, promotes the long-term survival of most of the SMNs in serum-free culture for 3 weeks. These findings provide useful culture conditions for studying the properties of SMNs and have implications for the treatment of motor neuron diseases.

摘要

许多肽类营养因子可促进高度纯化的胚胎脊髓运动神经元(SMNs)在培养中的短期存活,这些因子包括脑源性神经营养因子(BDNF)、睫状神经营养因子(CNTF)、成纤维细胞生长因子(FGF)、胶质细胞源性神经营养因子(GDNF)和肝细胞生长因子(HGF)。我们探究了这些肽类是否足以促进纯化的E15 SMNs的长期存活。与之前的报道相反,我们发现当SMNs在仅含有单一肽类营养因子的无血清培养基中培养时,只有约三分之一的细胞在培养3天后存活。当多种因子联合使用时,对存活有短暂的相加效应,但培养7天后,大多数SMNs已死亡。令人惊讶的是,当cAMP水平升高时,即使在低密度培养条件下,大多数SMNs在没有肽类营养因子的情况下也能伸出突起并在培养中存活1周。五种肽类营养因子与cAMP升高相结合,可促进大多数SMNs在无血清培养中长达3周的长期存活。这些发现为研究SMNs的特性提供了有用的培养条件,并对运动神经元疾病的治疗具有启示意义。

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