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PI3KC2α-dependent and VPS34-independent generation of PI3P controls primary cilium-mediated autophagy in response to shear stress
被引:58
作者:

Boukhalfa, Asma
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Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France

Nascimbeni, Anna Chiara
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Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France

Ramel, Damien
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Paul Sabatier Univ, Inst Metab & Cardiovasc Dis, INSERM, UMR 1048, Toulouse, France Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France

Dupont, Nicolas
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Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France

Hirsch, Emilio
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Univ Torino, Mol Biotechnol Ctr, Dept Mol Biotechnol & Hlth Sci, Turin, Italy Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France

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Laffargue, Muriel
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Paul Sabatier Univ, Inst Metab & Cardiovasc Dis, INSERM, UMR 1048, Toulouse, France Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France

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Morel, Etienne
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Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France
机构:
[1] Univ Paris 05, INEM, Sorbonne Paris Cite, INSERM U1151,CNRS,UMR 8253, Paris, France
[2] Paul Sabatier Univ, Inst Metab & Cardiovasc Dis, INSERM, UMR 1048, Toulouse, France
[3] Univ Torino, Mol Biotechnol Ctr, Dept Mol Biotechnol & Hlth Sci, Turin, Italy
关键词:
MEMBRANE;
ENDOCYTOSIS;
PHOSPHOINOSITIDES;
ACTIVATION;
PTDINS3P;
D O I:
10.1038/s41467-019-14086-1
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Cells subjected to stress situations mobilize specific membranes and proteins to initiate autophagy. Phosphatidylinositol-3-phosphate (PI3P), a crucial lipid in membrane dynamics, is known to be essential in this context. In addition to nutriments deprivation, autophagy is also triggered by fluid-flow induced shear stress in epithelial cells, and this specific autophagic response depends on primary cilium (PC) signaling and leads to cell size regulation. Here we report that PI3KC2 alpha, required for ciliogenesis and PC functions, promotes the synthesis of a local pool of PI3P upon shear stress. We show that PI3KC2 alpha depletion in cells subjected to shear stress abolishes ciliogenesis as well as the autophagy and related cell size regulation. We finally show that PI3KC2 alpha and VPS34, the two main enzymes responsible for PI3P synthesis, have different roles during autophagy, depending on the type of cellular stress: while VPS34 is clearly required for starvation-induced autophagy, PI3KC2 alpha participates only in shear stress-dependent autophagy.
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Curtin Univ, CHIRI Biosci, Sch Biomed Sci, Metab Signalling Grp, Perth, WA 6845, Australia Curtin Univ, CHIRI Biosci, Sch Biomed Sci, Metab Signalling Grp, Perth, WA 6845, Australia

Thompson, Philip E.
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机构:
Monash Univ, Monash Inst Pharmaceut Sci, Med Chem, Parkville Campus,381 Royal Parade, Parkville, Vic 3052, Australia Curtin Univ, CHIRI Biosci, Sch Biomed Sci, Metab Signalling Grp, Perth, WA 6845, Australia