Seipin is required for converting nascent to mature lipid droplets

Autor(en): Wang, Huajin
Becuwe, Michel
Housden, Benjamin E.
Chitraju, Chandramohan
Porras, Ashley J.
Graham, Morven M.
Liu, Xinran N.
Thiam, Abdou Rachid
Savage, David B.
Agarwal, Anil K.
Garg, Abhimanyu
Olarte, Maria-Jesus
Lin, Qingqing
Froehlich, Florian 
Hannibal-Bach, Hans Kristian
Upadhyayula, Srigokul
Perrimon, Norbert
Kirchhausen, Tomas
Ejsing, Christer S.
Walther, Tobias C.
Farese, Jr., Robert V.
Stichwörter: BIOGENESIS; Biology; CONGENITAL LIPODYSTROPHY; ENDOPLASMIC-RETICULUM; ER; FAT STORAGE; IDENTIFICATION; Life Sciences & Biomedicine - Other Topics; LIPODYSTROPHY PROTEIN SEIPIN; METABOLISM; TRIACYLGLYCEROL SYNTHESIS; YEAST
Erscheinungsdatum: 2016
Herausgeber: ELIFE SCIENCES PUBLICATIONS LTD
Journal: ELIFE
Volumen: 5
Zusammenfassung: 
How proteins control the biogenesis of cellular lipid droplets (LDs) is poorly understood. Using Drosophila and human cells, we show here that seipin, an ER protein implicated in LD biology, mediates a discrete step in LD formation-the conversion of small, nascent LDs to larger, mature LDs. Seipin forms discrete and dynamic foci in the ER that interact with nascent LDs to enable their growth. In the absence of seipin, numerous small, nascent LDs accumulate near the ER and most often fail to grow. Those that do grow prematurely acquire lipid synthesis enzymes and undergo expansion, eventually leading to the giant LDs characteristic of seipin deficiency. Our studies identify a discrete step of LD formation, namely the conversion of nascent LDs to mature LDs, and define a molecular role for seipin in this process, most likely by acting at ER-LD contact sites to enable lipid transfer to nascent LDs.
ISSN: 2050084X
DOI: 10.7554/eLife.16582

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