Specialized hepatocyte-like cells regulate Drosophila lipid metabolism

被引:306
作者
Gutierrez, Eugenio
Wiggins, David
Fielding, Barbara
Gould, Alex P.
机构
[1] Churchill Hosp, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LJ, England
[2] Natl Inst Med Res, MRC, London NW7 1AA, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1038/nature05382
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lipid metabolism is essential for growth and generates much of the energy needed during periods of starvation. In Drosophila, fasting larvae release large quantities of lipid from the fat body but it is unclear how and where this is processed. Here we identify the oenocyte as the principal cell type accumulating lipid droplets during starvation. Tissue-specific manipulations of the Slimfast amino-acid channel, the Lsd2 fat-storage regulator and the Brummer lipase indicate that oenocytes act downstream of the fat body. In turn, oenocytes are required for depleting stored lipid from the fat body during fasting. Hence, lipid-metabolic coupling between the fat body and oenocytes is bidirectional. When food is plentiful, oenocytes have critical roles in regulating growth, development and feeding behaviour. In addition, they specifically express many different lipid-metabolizing proteins, including Cyp4g1, an omega-hydroxylase regulating triacylglycerol composition. These findings provide evidence that some lipid-processing functions of the mammalian liver are performed in insects by oenocytes.
引用
收藏
页码:275 / 280
页数:6
相关论文
共 49 条
[1]   Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes [J].
Ashrafi, K ;
Chang, FY ;
Watts, JL ;
Fraser, AG ;
Kamath, RS ;
Ahringer, J ;
Ruvkun, G .
NATURE, 2003, 421 (6920) :268-272
[2]   Food level in relation to rate of development and eye pigmentation in Drosophila melanogaster [J].
Beadle, GW ;
Tatum, EL ;
Clancy, CW .
BIOLOGICAL BULLETIN, 1938, 75 (03) :447-462
[3]  
Britton JS, 1998, DEVELOPMENT, V125, P2149
[4]   Drosophila's insulin/P13-kinase pathway coordinates cellular metabolism with nutritional conditions [J].
Britton, JS ;
Lockwood, WK ;
Li, L ;
Cohen, SM ;
Edgar, BA .
DEVELOPMENTAL CELL, 2002, 2 (02) :239-249
[5]   EGF receptor signaling regulates pulses of cell delamination from the Drosophila ectoderm [J].
Brodu, V ;
Elstob, PR ;
Gould, AP .
DEVELOPMENTAL CELL, 2004, 7 (06) :885-895
[6]   Molecular mediators of hepatic steatosis and liver injury [J].
Browning, JD ;
Horton, JD .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (02) :147-152
[7]  
Burdge GC, 2000, BRIT J NUTR, V84, P781
[8]   ADIPOSE TISSUE OF DROSOPHILA MELANOGASTER .I. AN EXPERIMENTAL STUDY OF LARVAL FAT BODY [J].
BUTTERWORTH, FM ;
BODENSTEIN, D ;
KING, RC .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1965, 158 (02) :141-+
[9]   Fat metabolism in insects [J].
Canavoso, LE ;
Jouni, ZE ;
Karnas, KJ ;
Pennington, JE ;
Wells, MA .
ANNUAL REVIEW OF NUTRITION, 2001, 21 :23-46
[10]   EcR isoforms in Drosophila:: testing tissue-specific requirements by targeted blockade and rescue [J].
Cherbas, L ;
Hu, X ;
Zhimulev, I ;
Belyaeva, E ;
Cherbas, P .
DEVELOPMENT, 2003, 130 (02) :271-284