Lipid droplet-organelle interactions; sharing the fats

被引:208
作者
Murphy, Samantha
Martin, Sally [1 ]
Parton, Robert G.
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2009年 / 1791卷 / 06期
基金
英国医学研究理事会;
关键词
Motility; Lipid droplet; Microtubule; Organelle interaction; Caveolae; Rab GTPase; PROTEIN-KINASE-A; HORMONE-SENSITIVE LIPASE; DOMINANT-NEGATIVE MUTANT; WHITE ADIPOSE-TISSUE; ENDOPLASMIC-RETICULUM; MEMBRANE-FUSION; RAB GTPASES; INTRACELLULAR TRAFFICKING; TYROSINE PHOSPHORYLATION; PRIMARY CULTURE;
D O I
10.1016/j.bbalip.2008.07.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipid droplets (LDs) are key cellular organelles involved in lipid storage and mobilisation. While the major signalling cascades and many of the regulators of lipolysis have been identified, the cellular interactions involved in lipid mobilisation and release remain largely undefined. In non-adipocytes, LDs are small, mobile and interact with other cellular compartments. In contrast, adipocytes primarily contain very large, immotile LDs. The striking morphological differences between LDs in adipocytes and non-adipocytes suggest that key differences must exist in the manner in which LDs in different cell types interact with other organelles. Recent studies have highlighted the complexity of LD interactions, which can be both homotypic, with each other, and heterotypic, with other organelles. The molecules involved in these interactions are also now emerging. including Rab proteins, key regulators of membrane traffic, and caveolin, an integral membrane protein providing a functional link between the cell surface and LDs. Here we summarise recent insights into the cell biology of the LD particularly focussing on the homotypic and heterotypic interactions in both adipocytes and non-adipocytes. We speculate that these interactions may involve inter-organelle membrane contact sites or a hemi-fusion type mechanism to facilitate lipid transfer. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:441 / 447
页数:7
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