老化相关的自发荧光可作为细胞衰老的标志物

张静 杨璐萌 陈晓春*

doi:10.3969/j.issn.0529-1356.2014.01.001

解剖学报 >

2014 , Vol. 45 >Issue 1: 1 - 6

DOI: https://doi.org/10.3969/j.issn.0529-1356.2014.01.001

神经生物学

老化相关的自发荧光可作为细胞衰老的标志物

张静杨璐萌陈晓春*

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1.福建省高校脑老化与神经变性疾病重点实验室，福建省老年医学研究所，福州 350001;2.福建省分子神经病学重点实验室，福建医科大学附属协和医院神经内科，福州 350001

收稿日期: 2013-04-26

修回日期: 2013-07-08

网络出版日期: 2014-02-06

基金资助

国家重点基础研究发展计划973课题;福建省教育厅科技项目

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Aging related autofluorescence can be used as a marker of cell senescence

ZHANG Jing YANG Lu-meng CHEN Xiao-chun*

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1.Key Laboratory of Brain Aging and Neurodegenerative Disease, Fujian Institute of Geriatrics, Fuzhou 350001, China;2.Fujian Key Laboratory of Molecular Neurology, Department of Neurology, the Affiated Union Hospital of Fujian Medical University, Fuzhou 350001, China

Received date: 2013-04-26

Revised date: 2013-07-08

Online published: 2014-02-06

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摘要

目的观察衰老的脑组织内自发荧光的波长特点，探讨如何合理地利用和消减老化相关的自发荧光。方法选取3月龄和24月龄自然老化的C57BL/6J雌、雄性小鼠。以衰老相关β-半乳糖苷酶染色（SA-β-Gal）和脂褐素的沉积评估老年鼠脑组织衰老的程度。以激光共焦显微镜分析老化相关自发荧光的波长特点，免疫组织化学和免疫荧光的方法标记星形胶质细胞。结果老年鼠海马和下丘脑第三脑室室周旁出现强SA-β-Gal染色、脂褐素的聚集及自发荧光。老化相关的自发荧光发射波长介于500～565nm，下丘脑第三脑室室周旁的星形胶质细胞不仅高表达SA-β-Gal，而且出现很强的自发荧光。采用针对脂褐素的自发荧光消除剂处理脑组织后，老化相关的自发荧光几乎完全消失。结论老化相关的自发荧光可以作为特定表型细胞衰老的标志物；恰当的处理老化相关的自发荧光，可极大的提高衰老脑组织免疫荧光检测的特异性。

关键词： 衰老; 脑; 脂褐素; 自发荧光; 免疫荧光; 小鼠

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张静杨璐萌陈晓春* . 老化相关的自发荧光可作为细胞衰老的标志物[J]. 解剖学报, 2014 , 45(1) : 1 -6 . DOI: 10.3969/j.issn.0529-1356.2014.01.001

Abstract

Objective To describe the emission spectra of autofluorescence derived from lipofuscin in aged brain sections and to investigate how aging related autofluorescence is used reasonably and abolished properly. Methods Three months old and 24 months old C57BL/6J male and female mice were used in this study. Staining of senescenceassociated beta galatosidase and accumulation of lipofuscin were used to evaluate the degree of brain aging. Laser confocal microscopy was used to analyze the emission spectra of autofluorescence. Immunohistochemistry and immunofluorescence was used to identify astrocyte. Results Strong SA-β-Gal staining and autofluorescence and accumulation of lipofuscin appeared in the CA3 of hippocampus and the periventricular area of the third ventricle in 24 months old mice. The emission wavelength of aging related autofluorescence was between 500-565 nm. Astrocytes in periventricular area of the third ventricle were of not only strong SA-β-Gal staining, but also strong autofluorescence. Abolition of background autofluorescence from lipofuscin following immersion in autofluorescence eliminator reagent was observed in aged brain tissue. Conclusion Aging related autofluorescence can be used as a marker of cell senescence with a specific phenotype. Reduction of background autofluorescence from lipofuscin can improve the specificity of immunofluorescence detection in aged brain tissue samples.

Key words： Senescence; Brain; Lipofuscin; Autofluorescence; Immunofluorescence; Mouse

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