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Merck
CN

Atg5 regulates late endosome and lysosome biogenesis.

Science China. Life sciences (2013-12-27)
Junya Peng, Ran Zhang, Yitong Cui, Haodong Liu, Xiaoxin Zhao, Lei Huang, Mingxu Hu, Xiaoxi Yuan, Benyu Ma, Xiaowei Ma, Ueno Takashi, Komatsu Masaaki, Xingjie Liang, Li Yu
ABSTRACT

Autophagy is an evolutionarily conserved lysosome-based degradation process. Atg5 plays a very important role in autophagosome formation. Here we show that Atg5 is required for biogenesis of late endosomes and lysosomes in an autophagy-independent manner. In Atg5 (-/-) cells, but not in other essential autophagy genes defecting cells, recycling and retrieval of late endosomal components from hybrid organelles are impaired, causing persistent hybrid organelles and defective formation of late endosomes and lysosomes. Defective retrieval of late endosomal components from hybrid organelles resulting from impaired recruitment of a component of V1-ATPase to acidic organelles blocks the pH-dependent retrieval of late endosomal components from hybrid organelles. Lowering the intracellular pH restores late endosome/lysosome biogenesis in Atg5 (-/-) cells. Our data demonstrate an unexpected role of Atg5 and shed new light on late endosome and lysosome biogenesis.

MATERIALS
Product Number
Brand
Product Description

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Fluorescein isothiocyanate–dextran, average mol wt 60,000-76,000
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Leupeptin, microbial, ≥90% (HPLC)
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Lysosome Isolation Kit, sufficient for 25 g (tissue), sufficient for 20 mL (packed cells), enrichment of lysosomes from tissues and packed cells