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细胞钙成像作为研究神经元-胶质细胞回路的可靠方法。

Cell Calcium Imaging as a Reliable Method to Study Neuron-Glial Circuits.

作者信息

de Melo Reis Ricardo Augusto, Freitas Hércules Rezende, de Mello Fernando Garcia

机构信息

Laboratório de Neuroquímica, Instituto de Biofísica Carlos Chagas Filho, CCS, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

Department of Pathology and Laboratory Medicine, MIND Institute, University of California, Davis, Sacramento, CA, United States.

出版信息

Front Neurosci. 2020 Oct 2;14:569361. doi: 10.3389/fnins.2020.569361. eCollection 2020.

Abstract

Complex dynamic cellular networks have been studied in physiological and pathological processes under the light of single-cell calcium imaging (SCCI), a method that correlates functional data based on calcium shifts operated by different intracellular and extracellular mechanisms integrated with their cell phenotypes. From the classic synaptic structure to tripartite astrocytic model or the recent quadripartite microglia added ensemble, as well as other physiological tissues, it is possible to follow how cells signal spatiotemporally to cellular patterns. This methodology has been used broadly due to the universal properties of calcium as a second messenger. In general, at least two types of receptor operate through calcium permeation: a fast-acting ionotropic receptor channel and a slow-activating metabotropic receptor, added to exchangers/transporters/pumps and intracellular Ca release activated by messengers. These prototypes have gained an enormous amount of information in dynamic signaling circuits. SCCI has also been used as a method to associate phenotypic markers during development and stage transitions in progenitors, stem, vascular cells, neuro- and glioblasts, neurons, astrocytes, oligodendrocytes, and microglia that operate through ion channels, transporters, and receptors. Also, cancer cells or inducible cell lines from human organoids characterized by transition stages are currently being used to model diseases or reconfigure healthy cells in terms of the expression of calcium-binding/permeable molecules and shed light on therapy.

摘要

在单细胞钙成像(SCCI)的视角下,人们对生理和病理过程中的复杂动态细胞网络进行了研究。单细胞钙成像这种方法能将基于不同细胞内和细胞外机制所引发的钙变化的功能数据,与细胞表型关联起来。从经典的突触结构到三方星形胶质细胞模型,再到最近新增的四方小胶质细胞组合,以及其他生理组织,都能够追踪细胞如何在时空上向细胞模式发出信号。由于钙作为第二信使具有普遍特性,这种方法已被广泛应用。一般来说,至少有两种类型的受体通过钙渗透发挥作用:一种是快速作用的离子otropic受体通道,另一种是缓慢激活的代谢otropic受体,此外还有交换器/转运体/泵以及由信使激活的细胞内钙释放。这些原型在动态信号回路中已获取了大量信息。单细胞钙成像还被用作一种方法,用于在祖细胞、干细胞、血管细胞、神经母细胞和胶质母细胞、神经元、星形胶质细胞、少突胶质细胞和小胶质细胞的发育及阶段转变过程中关联表型标记,这些细胞通过离子通道、转运体和受体发挥作用。此外,目前正在使用癌细胞或来自具有转变阶段特征的人类类器官的可诱导细胞系,来模拟疾病或根据钙结合/可渗透分子的表达对健康细胞进行重新配置,并为治疗提供线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b6/7566175/61d99bf8d21d/fnins-14-569361-g001.jpg

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