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一种用于小鼠背根神经节体外形态功能分析的改进方法。

An improved method for in vitro morphofunctional analysis of mouse dorsal root ganglia.

作者信息

Ciglieri E, Ferrini F, Boggio E, Salio C

机构信息

Department of Veterinary Sciences, University of Turin, Largo Braccini 2, 10095 Grugliasco, TO, Italy.

Department of Veterinary Sciences, University of Turin, Largo Braccini 2, 10095 Grugliasco, TO, Italy.

出版信息

Ann Anat. 2016 Sep;207:62-7. doi: 10.1016/j.aanat.2016.04.032. Epub 2016 May 17.

Abstract

Sensory neurons in dorsal root ganglia (DRGs) are the first-order neurons along the pathway conveying sensory information from the periphery to the central nervous system. The analysis of the morphological and physiological features of these neurons and their alterations in pathology is the necessary prerequisite to understand pain encoding mechanisms. Here, we describe an in vitro procedure for combined morphofunctional analysis of mouse DRGs. Freshly excised DRGs obtained from adult mice were incubated in collagenase to dissolve the ensheathing connective capsule. The degradation of the connective tissue facilitates both access to the neurons by classical recording glass pipettes and the penetration of primary antibodies for immunohistochemical procedures. The entire DRGs were then imaged using a confocal microscope obtaining a fine 3D representation of their cytoarchitecture without requiring tissue sectioning. Thus, our proposed whole-mount preparation represents a flexible in vitro approach for both functional and phenotypic analysis of DRG neurons by at the same time preserving their neuroanatomical relationships.

摘要

背根神经节(DRG)中的感觉神经元是沿从外周向中枢神经系统传递感觉信息的通路的一级神经元。分析这些神经元的形态和生理特征及其在病理状态下的改变是理解疼痛编码机制的必要前提。在此,我们描述了一种用于小鼠背根神经节形态功能联合分析的体外方法。从成年小鼠新鲜切除的背根神经节在胶原酶中孵育以溶解包裹性结缔组织囊。结缔组织的降解既便于经典记录玻璃微吸管接近神经元,也便于一抗穿透用于免疫组织化学程序。然后使用共聚焦显微镜对整个背根神经节进行成像,无需组织切片即可获得其细胞结构的精细三维图像。因此,我们提出的整装标本制备方法是一种灵活的体外方法,可同时对背根神经节神经元进行功能和表型分析,同时保留它们的神经解剖关系。

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