Seipin is required for converting nascent to mature lipid droplets

Huajin Wang(Boston University), Michel Becuwe(Boston University), Benjamin E. Housden(Harvard University), Chandramohan Chitraju(Boston University), Ashley J Porras(Boston University), Morven Graham(Yale University), Xinran N Liu(Yale University), Abdou Rachid Thiam(Centre National de la Recherche Scientifique), David B. Savage(University of Cambridge), Anil K. Agarwal(Southwestern Medical Center), Abhimanyu Garg(Southwestern Medical Center), Maria-Jesus Olarte(Boston University), Qingqing Lin(Boston University), Florian Fröhlich(Boston University), Hans Kristian Hannibal‐Bach(University of Southern Denmark), Srigokul Upadhyayula(Boston University), Norbert Perrimon(Howard Hughes Medical Institute), Tomas Kirchhausen(Boston University), Christer S. Ejsing(University of Southern Denmark), Tobias C. Walther(Broad Institute), Robert V. Farese(Broad Institute)
eLife
August 26, 2016
Cited by 398Open Access
Full Text

Abstract

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.


Related Papers

No related papers found

Powered by citation graph analysis