Probing Peroxisome Dynamics and Biogenesis by Fluorescence Imaging

过氧化物酶体 生物发生 细胞器 细胞生物学 生物 细胞器生物发生 活体细胞成像 计算生物学 生物化学 细胞 基因
作者
Miluska Jauregui,Peter K. Kim
出处
期刊:Current protocols in cell biology [Wiley]
卷期号:62 (1): 21.9.1-21.9.20 被引量:3
标识
DOI:10.1002/0471143030.cb2109s62
摘要

Abstract Peroxisomes are the most recently discovered classical organelles, and only lately have their diverse functions been truly recognized. Peroxisomes are highly dynamic structures, changing both morphologically and in number in response to both extracellular and intracellular signals. This metabolic organelle came to prominence due to the many genetic disorders caused by defects in its biogenesis or enzymatic functions. There is now growing evidence that suggests peroxisomes are involved in lipid biosynthesis, innate immunity, redox homeostasis, and metabolite scavenging, among other functions. Therefore, it is important to have available suitable methods and techniques to visualize and quantify peroxisomes in response to various cellular signals. This unit includes a number of protocols that will enable researchers to image, qualify, and quantify peroxisome numbers and morphology—with both steady‐state and time‐lapse imaging using mammalian cells. The use of photoactivatable fluorescent proteins to detect and measure peroxisome biogenesis is also described. Altogether, the protocols described here will facilitate understanding of the dynamic changes that peroxisomes undergo in response to various cellular signals. Curr. Protoc. Cell Biol . 62:21.9.1‐21.9.20. © 2014 by John Wiley & Sons, Inc.
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