Fsp27 promotes lipid droplet growth by lipid exchange and transfer at lipid droplet contact sites

被引:295
作者
Gong, Jingyi [1 ]
Sun, Zhiqi [1 ]
Wu, Lizhen [1 ]
Xu, Wenyi [1 ]
Schieber, Nicole [2 ,3 ]
Xu, Dijin [1 ]
Shui, Guanghou [4 ]
Yang, Hongyuan [5 ]
Parton, Robert G. [2 ,3 ]
Li, Peng [1 ]
机构
[1] Tsinghua Univ, Peking Tsinghua Ctr Life Sci, Beijing 100084, Peoples R China
[2] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[3] Univ Queensland, Ctr Microscopy & Microanal, Brisbane, Qld 4072, Australia
[4] Natl Univ Singapore, Inst Life Sci, Singapore 119077, Singapore
[5] Univ New S Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW 2052, Australia
基金
中国国家自然科学基金; 英国医学研究理事会;
关键词
FAT-SPECIFIC PROTEIN-27; INSULIN SENSITIVITY; DEFICIENT MICE; CIDEA; DEGRADATION; STEATOSIS; RESISTANT; STORAGE;
D O I
10.1083/jcb.201104142
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lipid droplets (LDs) are dynamic cellular organelles that control many biological processes. However, molecular components determining LD growth are poorly understood. Genetic analysis has indicated that Fsp27, an LD-associated protein, is important in controlling LD size and lipid storage in adipocytes. In this paper, we demonstrate that Fsp27 is focally enriched at the LD-LD contacting site (LDCS). Photobleaching revealed the occurrence of lipid exchange between contacted LDs in wild-type adipocytes and Fsp27-overexpressing cells but not Fsp27-deficient adipocytes. Furthermore, live-cell imaging revealed a unique Fsp27-mediated LD growth process involving a directional net lipid transfer from the smaller to larger LDs at LDCSs, which is in accordance with the biophysical analysis of the internal pressure difference between the contacting LD pair. Thus, we have uncovered a novel molecular mechanism of LD growth mediated by Fsp27.
引用
收藏
页码:953 / 963
页数:11
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