Receptor-mediated internalization promotes increased endosome size and number in a RAB4-and RAB5-dependent manner

被引:4
|
作者
Naslavsky, Naava [1 ,2 ]
Caplan, Steve [1 ,2 ]
机构
[1] Univ Nebraska Med Ctr, Dept Biochem & Mol Biol, Omaha, NE 68198 USA
[2] Univ Nebraska Med Ctr, Fred & Pamela Buffett Canc Ctr, Omaha, NE 68198 USA
基金
美国国家卫生研究院;
关键词
Internalization; Endosome size; Endosome number; RAB4; RAB5; RAB8A; RAB10; RAB11A; EPIDERMAL-GROWTH-FACTOR; BINDING PROTEIN RAB4; BASOLATERAL TRANSPORT; TRANSFERRIN RECEPTOR; COATED VESICLES; EEA1; COMPLEX; MICROVESICLES; LOCALIZATION; TRAFFICKING;
D O I
10.1016/j.ejcb.2023.151339
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Despite their significance in receptor-mediated internalization and continued signal transduction in cells, early/ sorting endosomes (EE/SE) remain incompletely characterized, with many outstanding questions that surround the dynamics of their size and number. While several studies have reported increases in EE/SE size and number resulting from endocytic events, few studies have addressed such dynamics in a methodological and quantitative manner. Herein we apply quantitative fluorescence microscopy to measure the size and number of EE/SE upon internalization of two different ligands: transferrin and epidermal growth factor. Additionally, we used siRNA knock-down to determine the involvement of 5 different endosomal RAB proteins (RAB4, RAB5, RAB8A, RAB10 and RAB11A) in EE/SE dynamics. Our study provides new information on the dynamics of endosomes during endocytosis, an important reference for researchers studying receptor-mediated internalization and endocytic events.
引用
收藏
页数:9
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