Seipin is required for converting nascent to mature lipid droplets

Author:

Wang Huajin123,Becuwe Michel23,Housden Benjamin E4,Chitraju Chandramohan23,Porras Ashley J23,Graham Morven M5,Liu Xinran N5,Thiam Abdou Rachid6,Savage David B7,Agarwal Anil K8,Garg Abhimanyu8,Olarte Maria-Jesus23,Lin Qingqing23,Fröhlich Florian239,Hannibal-Bach Hans Kristian10,Upadhyayula Srigokul31112,Perrimon Norbert413,Kirchhausen Tomas31112,Ejsing Christer S10,Walther Tobias C231314,Farese Robert V2314ORCID

Affiliation:

1. Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, United States

2. Department of Genetics and Complex Diseases, Harvard T H Chan School of Public Health, Boston, United States

3. Department of Cell Biology, Harvard Medical School, Boston, United States

4. Department of Genetics, Harvard Medical School, Boston, United States

5. Center for Cellular and Molecular Imaging, Department of Cell Biology, Yale School of Medicine, New Haven, United States

6. Laboratoire de Physique Statistique, École Normale Supérieure, PSL Research University, Université Paris Diderot Sorbonne Paris-Cité, Sorbonne Universités UPMC Univ Paris 06, CNRS UMR 8550, Paris, France

7. The University of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Cambridge, United Kingdom

8. Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, United States

9. Molecular Membrane Biology Section, Department of Biology/Chemistry, University of Osnabrück, Osnabrück, Germany

10. VILLUM Center for Bioanalytical Sciences, Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark

11. Department of Pediatrics, Harvard Medical School, Boston, United States

12. Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, United States

13. Howard Hughes Medical Institute, Boston, United States

14. Broad Institute of Harvard and MIT, Cambridge, United States

Abstract

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.

Funder

Canadian Institutes of Health Research

European Molecular Biology Organization

Wellcome Trust

NIHR Cambridge Biomedical Research Centre

Howard Hughes Medical Institute

Biogen

National Institutes of Health

Villum Fonden

Strategiske Forskningsråd

G Harold and Leila Y. Mathers Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference45 articles.

1. Seipin: a mysterious protein;Agarwal;Trends in Molecular Medicine,2004

2. Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy;Agarwal;The Journal of Clinical Endocrinology & Metabolism,2003

3. Comprehensive lipidome analysis by shotgun lipidomics on a hybrid quadrupole-orbitrap-linear ion trap mass spectrometer;Almeida;Journal of the American Society for Mass Spectrometry,2015

4. Seipin promotes adipose tissue fat storage through the ER Ca²⁺-ATPase SERCA;Bi;Cell Metabolism,2014

5. Seipin is a discrete homooligomer;Binns;Biochemistry,2010

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