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使用BrdU掺入的流式细胞术分析作为一种测量小鼠成年神经发生的高通量方法。

Flow cytometric analysis of BrdU incorporation as a high-throughput method for measuring adult neurogenesis in the mouse.

作者信息

Balu Darrick T, Hodes Georgia E, Hill Tiffany E, Ho Nancy, Rahman Zia, Bender Corey N, Ring Robert H, Dwyer Jason M, Rosenzweig-Lipson Sharon, Hughes Zoe A, Schechter Lee E, Lucki Irwin

机构信息

Department of Pharmacology, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

J Pharmacol Toxicol Methods. 2009 Mar-Apr;59(2):100-7. doi: 10.1016/j.vascn.2008.12.002. Epub 2008 Dec 14.

Abstract

INTRODUCTION

The generation of new neurons occurs throughout adulthood in discrete brain regions, and may be regulated by neuropsychiatric diseases and therapeutic drug treatments. Most current methods that study this process measure the labeling of newborn cells by 5-bromo-2-deoxyuridine (BrdU) using immunohistochemical methods followed by the microscopic counting of BrdU positive cells. This method is time consuming and labor intensive, typically taking several weeks to analyze.

METHODS

Therefore, we characterized a method to measure BrdU incorporation in the adult mouse hippocampus in vivo by using flow cytometry, which normally allows analysis of data within a single day.

RESULTS

The present study compared multiple BrdU dosing and loading protocols to determine a dosing strategy that produced the best signal to noise ratio. BrdU incorporation was also compared across different brain regions. The method was sensitive to a number of experimental disease manipulations. Induction of type-1 diabetes and depletion of norepinephrine reduced hippocampal cell proliferation. In contrast, chronic administration of electroconvulsive shock, a somatic treatment for depression, as well as chronic treatment with the antidepressant fluoxetine elevated hippocampal cell proliferation. This increase in cell proliferation with fluoxetine was detected as early as 14 days into treatment. Moreover, comparing measures of cell proliferation obtained by immunohistochemical and flow cytometric methods within the same animals were convergent and significantly correlated to each other. Flow cytometry was also sufficiently sensitive to quantify the survival of newly born cells.

DISCUSSION

These experiments validate the utility of flow cytometry in analyzing hippocampal cell proliferation and survival in a reliable and high-throughput fashion. The speedy analysis afforded by flow cytometry lends itself to be utilized in novel drug discovery and physiology.

摘要

引言

成年期新神经元在离散的脑区中持续产生,可能受神经精神疾病和治疗性药物治疗的调节。目前大多数研究这一过程的方法是使用免疫组织化学方法,通过5-溴-2-脱氧尿苷(BrdU)标记新生细胞,然后在显微镜下对BrdU阳性细胞进行计数。这种方法既耗时又费力,通常需要几周时间来分析。

方法

因此,我们描述了一种通过流式细胞术在成年小鼠体内测量海马体中BrdU掺入的方法,该方法通常可以在一天内完成数据分析。

结果

本研究比较了多种BrdU给药和加载方案,以确定产生最佳信噪比的给药策略。还比较了不同脑区的BrdU掺入情况。该方法对多种实验性疾病操作敏感。1型糖尿病的诱导和去甲肾上腺素的消耗会降低海马体细胞增殖。相反,慢性给予电休克治疗(一种抑郁症的躯体治疗方法)以及慢性给予抗抑郁药氟西汀会提高海马体细胞增殖。氟西汀治疗14天后就检测到细胞增殖增加。此外,在同一动物体内通过免疫组织化学和流式细胞术方法获得的细胞增殖测量结果相互趋同且显著相关。流式细胞术也足够灵敏,能够量化新生细胞的存活率。

讨论

这些实验验证了流式细胞术在以可靠且高通量的方式分析海马体细胞增殖和存活方面的实用性。流式细胞术提供的快速分析适用于新药发现和生理学研究。

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