TY - JOUR
T1 - Rab5 activation on macropinosomes requires ALS2, and subsequent Rab5 inactivation through ALS2 detachment requires active Rab7
AU - Morishita, So
AU - Wada, Naoyuki
AU - Fukuda, Mitsunori
AU - Nakamura, Takeshi
N1 - Funding Information:
We thank Dr M. Matsuda (Kyoto University) and Dr T. Yoshimori (Osaka University) for plasmids. We also thank Dr N. Mochizuki (NCVC Research Institute) for anti-GFP polyclonal antibodies. We thank K. Nakamura for technical assistance and members of the Nakamura laboratory for their input. This work was supported by grants from JSPS KAKENHI (15K06782).
Publisher Copyright:
© 2018 Federation of European Biochemical Societies
PY - 2019/1
Y1 - 2019/1
N2 - Macropinocytosis is a nonspecific bulk uptake of extracellular fluid. During endosome maturation, the Rab5-to-Rab7 switch machinery executes the conversion from early to late endosomes. However, how the Rab switch works during macropinosome maturation remains unclear. Here, we elucidate the Rab switch machinery in macropinosome maturation using Förster resonance energy transfer imaging. Rab5 is activated and concurrently recruited to macropinosomes during ruffle closure. ALS2 depletion abolishes transient Rab5 activation on macropinosomes, while ALS2 is recruited to macropinosomes simultaneously with Rab5 activation. Thus, we conclude ALS2 activates Rab5 on macropinosomes. The absence of active Rab7 prolongs ALS2 presence and Rab5 activation on macropinosomes, indicating that active Rab7 is necessary for Rab5 inactivation through ALS2 dissociation and plays key roles in the Rab switch on macropinosomes.
AB - Macropinocytosis is a nonspecific bulk uptake of extracellular fluid. During endosome maturation, the Rab5-to-Rab7 switch machinery executes the conversion from early to late endosomes. However, how the Rab switch works during macropinosome maturation remains unclear. Here, we elucidate the Rab switch machinery in macropinosome maturation using Förster resonance energy transfer imaging. Rab5 is activated and concurrently recruited to macropinosomes during ruffle closure. ALS2 depletion abolishes transient Rab5 activation on macropinosomes, while ALS2 is recruited to macropinosomes simultaneously with Rab5 activation. Thus, we conclude ALS2 activates Rab5 on macropinosomes. The absence of active Rab7 prolongs ALS2 presence and Rab5 activation on macropinosomes, indicating that active Rab7 is necessary for Rab5 inactivation through ALS2 dissociation and plays key roles in the Rab switch on macropinosomes.
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U2 - 10.1002/1873-3468.13306
DO - 10.1002/1873-3468.13306
M3 - Article
C2 - 30485418
AN - SCOPUS:85058147459
SN - 0014-5793
VL - 593
SP - 230
EP - 241
JO - FEBS Letters
JF - FEBS Letters
IS - 2
ER -