Cytosolic lipid droplets increase in size by microtubule-dependent complex formation

被引:145
作者
Boström, P
Rutberg, M
Ericsson, J
Holmdahl, P
Andersson, L
Frohman, MA
Borén, J
Olofsson, SO [1 ]
机构
[1] Univ Gothenburg, Sahlgrenska Univ Hosp, Wallenberg Lab Cardiovasc Res, SE-41345 Gothenburg, Sweden
[2] Holmdahl Biotech, Gothenburg, Sweden
[3] SUNY Stony Brook, Ctr Dev Genet, Stony Brook, NY 11794 USA
[4] SUNY Stony Brook, Dept Pharmacol Sci, Stony Brook, NY 11794 USA
关键词
lipid droplets; lipid droplet fusion; adipocyte differentiation protein; microtubules;
D O I
10.1161/01.ATV.0000179676.41064.d4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives - Adipocyte differentiation- related protein ( ADRP)- containing lipid droplets have an essential role in the development of insulin resistance and atherosclerosis. Such droplets form in a cell-free system with a diameter of 0.1 to 0.4 mu m, while the droplets present in cells vary in size, from small to very large, suggesting that the droplets can increase in size after being assembled. We have addressed this possibility. Methods and Results - Experiments in NIH 3T3 cells demonstrated that the lipid droplets could increase in size independently of triglyceride biosynthesis. NIH 3T3 cells were either microinjected with ADRP - GFP ( green fluorescent protein) or stained with Nile Red and followed by confocal microscopy and time-lapse recordings. The results showed that lipid droplets formed complexes with each other, with a volume equal to the sum of the merging particles. The formation of complexes could be inhibited by the nocodazole-induced depolymerization of the microtubules; thus, the process is dependent on microtubules. The presence of dynein on ADRP-containing droplets supports a role for this motor protein. Conclusions - Lipid droplets can grow after they have been assembled. This increase in size is independent of triglyceride biosynthesis and involves formation of complexes, which requires intact microtubules.
引用
收藏
页码:1945 / 1951
页数:7
相关论文
共 22 条
[1]   The cellular biology of eosinophil eicosanoid formation and function [J].
Bandeira-Melo, C ;
Bozza, PT ;
Weller, PF .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 109 (03) :393-400
[2]   Extranuclear lipid bodies, elicited by CCR3-mediated signaling pathways, are the sites of chemokine-enhanced leukotriene C4 production in eosinophils and basophils [J].
Bandeira-Melo, C ;
Phoofolo, M ;
Weller, PF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (25) :22779-22787
[3]   Arachidonyl trifluoromethyl ketone induces lipid body formation in leukocytes [J].
Bozza, PT ;
Weller, PF .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2001, 64 (4-5) :227-230
[4]   Proteomic analysis of proteins associated with lipid droplets of basal and lipolytically stimulated 3T3-L1 adipocytes [J].
Brasaemle, DL ;
Dolios, G ;
Shapiro, L ;
Wang, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (45) :46835-46842
[5]  
Brasaemle DL, 1997, J LIPID RES, V38, P2249
[6]   Molecular mediators of hepatic steatosis and liver injury [J].
Browning, JD ;
Horton, JD .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (02) :147-152
[7]   Possible involvement of protein kinase C in the induction of adipose differentiation-related protein by sterol ester in RAW 264.7 macrophages [J].
Chen, JS ;
Greenberg, AS ;
Tseng, YZ ;
Wang, SM .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2001, 83 (02) :187-199
[8]   Hepatic steatosis: A mediator of the metabolic syndrome. Lessons from animal models [J].
den Boer, M ;
Voshol, PJ ;
Kuipers, F ;
Havekes, LM ;
Romijn, JA .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (04) :644-649
[9]   Phospholipase A2 [J].
Diaz, BL ;
Arm, JP .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2003, 69 (2-3) :87-97
[10]   Mechanisms of disease - Inflammation, atherosclerosis, and coronary artery disease [J].
Hansson, GK .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (16) :1685-1695