Adult Drosophila melanogaster as a model for the study of glucose homeostasis

被引:45
作者
Haselton, Aaron T. [2 ]
Fridell, Yih-Woei C. [1 ]
机构
[1] Univ Connecticut, Dept Allied Hlth Sci, Storrs, CT 06269 USA
[2] SUNY Albany, Dept Biol, New Paltz, NY 12561 USA
来源
AGING-US | 2010年 / 2卷 / 08期
关键词
Drosophila insulin-like peptides (DILPs); DILP-producing cells (IPCs); Insulin/Insulin-like growth factor signaling (IIS); hemolymph; adipokinetic hormone (AKH); INSULIN-PRODUCING NEURONS; LIFE-SPAN; CELLS; GROWTH; ABLATION; PEPTIDES;
D O I
10.18632/aging.100185
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Genetic ablation of Drosophila melanogaster insulin-like peptide (DILP) and adipokinetic hormone-producing cells accompanied by cell biological and metabolic measurements have revealed functional conservation in nutrient sensing and the underlying signaling mechanisms between mammal and fruit fly. Despite significant advances gained in understanding the neuroendocrine responses to nutrient changes during developmental larval stages, we discuss here the need for investigating glucose homeostasis in the post-mitotic adult stage as the result of ablation of DILP producing cells (IPCs). Our recent studies demonstrate that while both constitutive and adult-specific partial ablation of IPCs renders those flies hyperglycemic and glucose intolerant, flies with adult-specific IPC ablation remain insulin sensitive. Our results substantiate a role of adult IPCs in modulating aspects of glucose homeostasis and highlight the complexity in DILP action in the adult fly.
引用
收藏
页码:523 / 526
页数:4
相关论文
共 13 条
[1]   An evolutionarily conserved function of the Drosophila insulin receptor and insulin-like peptides in growth control [J].
Brogiolo, W ;
Stocker, H ;
Ikeya, T ;
Rintelen, F ;
Fernandez, R ;
Hafen, E .
CURRENT BIOLOGY, 2001, 11 (04) :213-221
[2]   Longer lifespan, altered metabolism, and stress resistance in Drosophila from ablation of cells making insulin-like ligands [J].
Broughton, SJ ;
Piper, MDW ;
Ikeya, T ;
Bass, TM ;
Jacobson, J ;
Driege, Y ;
Martinez, P ;
Hafen, E ;
Withers, DJ ;
Leevers, SJ ;
Partridge, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (08) :3105-3110
[3]   Making metabolic decisions in Drosophila [J].
Buch, Susanne ;
Pankratz, Michael J. .
FLY, 2009, 3 (01) :74-77
[4]   Increased uncoupling protein (UCP) activity in Drosophila insulin-producing neurons attenuates insulin signaling and extends lifespan [J].
Fridell, Yih-Woei C. ;
Hoh, Melissa ;
Kreneisz, Orsolya ;
Hosier, Suzanne ;
Chang, Chengyi ;
Scantling, Dane ;
Mulkey, Daniel K. ;
Helfand, Stephen L. .
AGING-US, 2009, 1 (08) :699-713
[5]   Remote Control of Insulin Secretion by Fat Cells in Drosophila [J].
Geminard, Charles ;
Rulifson, Eric J. ;
Leopold, Pierre .
CELL METABOLISM, 2009, 10 (03) :199-207
[6]   On the cusp of change or chimera? [J].
Hasegawa, Harukiyo .
ASIAN BUSINESS & MANAGEMENT, 2010, 9 (01) :1-3
[7]   Nutrient-dependent expression of insulin-like peptides from neuroendocrine cells in the CNS contributes to growth regulation in Drosophila [J].
Ikeya, T ;
Galic, M ;
Belawat, P ;
Nairz, K ;
Hafen, E .
CURRENT BIOLOGY, 2002, 12 (15) :1293-1300
[8]   Conserved mechanisms of glucose sensing and regulation by Drosophila corpora cardiaca cells [J].
Kim, SK ;
Rulifson, EJ .
NATURE, 2004, 431 (7006) :316-320
[9]   Hemolymph sugar homeostasis and starvation-induced hyperactivity affected by genetic manipulations of the adipokinetic hormone-encoding gene in Drosophila melanogaster [J].
Lee, GH ;
Park, JH .
GENETICS, 2004, 167 (01) :311-323
[10]   Mitochondrial dysfunction and type 2 diabetes [J].
Lowell, BB ;
Shulmanz, GI .
SCIENCE, 2005, 307 (5708) :384-387