Suppr超能文献

原代神经元培养物中细胞活力的评估。

Assessment of cell viability in primary neuronal cultures.

作者信息

Ying H S, Gottron F J, Choi D W

机构信息

Washington University School Of Medicine, St. Louis, Missouri, USA.

出版信息

Curr Protoc Neurosci. 2001 May;Chapter 7:Unit7.18. doi: 10.1002/0471142301.ns0718s13.

Abstract

Four commonly used methods for the assessment of neuronal (or glial) cell viability are described in this unit. The MTT assay is sensitive to the function of labile mitochondrial enzymes, which typically lose activity early in the progression towards death. The lactate dehydrogenase (LDH) assay measures the appearance of this cytosolic enzyme in the bathing medium, providing a measure of plasma membrane integrity. Loss of plasma membrane integrity is also the basis of the trypan blue dye assay and the propidium iodide assay. Trypan blue staining is assessed by cell counts; propidium iodide labeling can be assessed either by cell counts, typically in conjunction with fluorescein diacetate counterstaining to identify intact cells containing adequate levels of functional esterases, or with a fluorescence plate reader.

摘要

本单元介绍了四种常用的评估神经元(或神经胶质)细胞活力的方法。MTT 法对不稳定的线粒体酶功能敏感,这些酶通常在细胞死亡进程早期就会失去活性。乳酸脱氢酶(LDH)测定法通过检测胞质酶在培养液中的出现情况,来衡量细胞膜的完整性。细胞膜完整性的丧失也是台盼蓝染色法和碘化丙啶测定法的基础。台盼蓝染色通过细胞计数进行评估;碘化丙啶标记可通过细胞计数进行评估,通常与荧光素二乙酸复染相结合,以识别含有足够水平功能酯酶的完整细胞,也可使用荧光酶标仪进行评估。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验