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2
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本文引用的文献

1
A sympathetic neuron autonomous role for Egr3-mediated gene regulation in dendrite morphogenesis and target tissue innervation.Egr3 介导的基因调控在树突形态发生和靶组织神经支配中的交感神经元自主作用。
J Neurosci. 2013 Mar 6;33(10):4570-83. doi: 10.1523/JNEUROSCI.5481-12.2013.
2
Abnormal sympathetic nervous system development and physiological dysautonomia in Egr3-deficient mice.Egr3基因缺陷小鼠的交感神经系统发育异常和生理性自主神经功能障碍。
Development. 2008 Sep;135(17):2949-57. doi: 10.1242/dev.023960. Epub 2008 Jul 24.
3
Multiple channel interactions explain the protection of sympathetic neurons from apoptosis induced by nerve growth factor deprivation.多通道相互作用解释了交感神经元免受神经生长因子剥夺诱导的细胞凋亡的保护机制。
J Neurosci. 2002 Jan 1;22(1):114-22. doi: 10.1523/JNEUROSCI.22-01-00114.2002.

源自小鼠颈上神经节的神经元培养

Neuron Culture from Mouse Superior Cervical Ganglion.

作者信息

Jackson Marisa, Tourtellotte Warren

机构信息

Department of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, USA.

出版信息

Bio Protoc. 2014 Jan 20;4(2). doi: 10.21769/bioprotoc.1035.

DOI:10.21769/bioprotoc.1035
PMID:27054145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4819978/
Abstract

The rodent superior cervical ganglion (SCG) is a useful and readily accessible source of neurons for studying the mechanisms of sympathetic nervous system (SNS) development and growth The sympathetic nervous system (SNS) of early postnatal animals undergoes a great deal of remodeling and development; thus, neurons taken from mice at this age are primed to re-grow and establish synaptic connections after removal. The stereotypic location and size of the SCG make it ideal for rapid isolation and dissociation. The protocol described here details the requirements for the dissection, culture and differentiation of SCG neurons. The protocol is suitable for culturing neurons from late embryonic gestation to approximately postnatal day 3. The culture technique discussed below utilizes glass coverslips for the microscopic examination of fixed cells.

摘要

啮齿动物的颈上神经节(SCG)是研究交感神经系统(SNS)发育和生长机制的有用且易于获取的神经元来源。出生后早期动物的交感神经系统(SNS)会经历大量重塑和发育;因此,取自这个年龄段小鼠的神经元在被移除后易于重新生长并建立突触连接。颈上神经节的固定位置和大小使其成为快速分离和解离的理想选择。此处描述的方案详细说明了颈上神经节神经元解剖、培养和分化的要求。该方案适用于培养从胚胎后期到出生后约第3天的神经元。下面讨论的培养技术利用玻璃盖玻片对固定细胞进行显微镜检查。