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胶质细胞系源性神经营养因子(GDNF)在大鼠心脏发育早期可促进交感神经轴突生长。

Glial cell line-derived neurotrophic factor (GDNF) enhances sympathetic neurite growth in rat hearts at early developmental stages.

作者信息

Miwa Keiko, Lee Jong-Kook, Takagishi Yoshiko, Opthof Tobias, Fu Xianming, Kodama Itsuo

机构信息

Department of Cardiovascular Research, Research Institute of Environmental Medicine, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Japan.

出版信息

Biomed Res. 2010 Dec;31(6):353-61. doi: 10.2220/biomedres.31.353.

Abstract

Molecular signaling of sympathetic innervation of myocardium is an unresolved issue. The purpose of this study was to investigate the effect of neurotrophic factors on sympathetic neurite growth towards cardiomyocytes. Cardiomyocytes (CMs) and sympathetic neurons (SNs) were isolated from neonatal rat hearts and superior cervical ganglia, and were co-cultured, either in a random or localized way. Neurite growth from SNs toward CMs was assessed by immunohistochemistry for neurofilament M and α-actinin in response to neurotrophic factors-nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotrophic factor (GDNF), ciliary neurotrophic factor (CNTF) and a chemical repellent, semaphorin 3A. As a result, GDNF as well as NGF and BDNF stimulated neurite growth. GDNF enhanced neurite outgrowth even under the NGF-depleted culture condition, excluding an indirect effect of GDNF via NGF. Quantification of mRNA and protein by real-time PCR and immunohistochemistry at different developmental stages revealed that GDNF is abundantly expressed in the hearts of embryos and neonates, but not in adult hearts. GDNF plays an important role in inducing cardiac sympathetic innervation at the early developmental stages. A possible role in (re)innervation of injured or transplanted or cultured and transplanted myocardium may deserve investigation.

摘要

心肌交感神经支配的分子信号传导是一个尚未解决的问题。本研究的目的是探讨神经营养因子对交感神经突向心肌细胞生长的影响。从新生大鼠心脏和颈上神经节分离出心肌细胞(CMs)和交感神经元(SNs),并以随机或局部方式进行共培养。通过免疫组织化学检测神经丝M和α-辅肌动蛋白,评估SNs向CMs的神经突生长,以响应神经营养因子——神经生长因子(NGF)、脑源性神经营养因子(BDNF)、胶质细胞系源性神经营养因子(GDNF)、睫状神经营养因子(CNTF)和一种化学排斥剂——信号素3A。结果,GDNF以及NGF和BDNF刺激了神经突生长。即使在缺乏NGF的培养条件下,GDNF也能增强神经突的生长,排除了GDNF通过NGF产生的间接作用。通过实时PCR和免疫组织化学对不同发育阶段的mRNA和蛋白质进行定量分析,结果显示GDNF在胚胎和新生大鼠心脏中大量表达,但在成年心脏中不表达。GDNF在早期发育阶段诱导心脏交感神经支配中起重要作用。GDNF在损伤、移植或培养及移植心肌的(再)神经支配中可能发挥的作用值得研究。

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