Drosophila TNF/TNFRs: At the crossroad between metabolism, immunity, and tissue homeostasis

被引:12
作者
Colombani, Julien [1 ,2 ]
Andersen, Ditte S. [1 ,2 ]
机构
[1] Univ Copenhagen, Dept Biol, Copenhagen, Denmark
[2] Univ Copenhagen, Dept Biol, Univ Pk 15,Bldg 3, DK-2100 Copenhagen, Denmark
基金
欧洲研究理事会; 欧盟地平线“2020”;
关键词
Drosophila; immunity; metabolism; TNF; tumor; TUMOR-NECROSIS-FACTOR; INSULIN-PRODUCING CELLS; ONCOGENIC RAS; FACTOR-ALPHA; GENETIC SCREEN; TNF-ALPHA; RECEPTOR; EIGER; JNK; ACTIVATION;
D O I
10.1002/1873-3468.14716
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
Tumor necrosis factor (TNF)-a is a highly conserved proinflammatory cytokine with important functions in immunity, tissue repair, and cellular homeostasis. Due to the simplicity of the Drosophila TNF-TNF receptor (TNFR) system and a broad genetic toolbox, the fly has played a pivotal role in deciphering the mechanisms underlying TNF-mediated physiological and pathological functions. In this review, we summarize the recent advances in our understanding of how local and systemic sources of Egr/TNF contribute to its antitumor and tumor-promoting properties, and its emerging functions in adaptive growth responses, sleep regulation, and adult tissue homeostasis. The recent annotation of TNF as an adipokine and its indisputable contribution to obesity- and cancer-associated metabolic diseases have provoked a new area of research focusing on its dual function in regulating immunity and energy homeostasis. Here, we discuss the role of TNFR signaling in coupling immune and metabolic processes and how this might be relevant in the adaption of host to environmental stresses, or, in the case of obesity, promote metabolic derangements and disease.
引用
收藏
页码:2416 / 2432
页数:17
相关论文
共 72 条
[51]   Transformed Epithelia Trigger Non-Tissue-Autonomous Tumor Suppressor Response by Adipocytes via Activation of Toll and Eiger/TNF Signaling [J].
Parisi, Federica ;
Stefanatos, Rhoda K. ;
Strathdee, Karen ;
Yu, Yachuan ;
Vidal, Marcos .
CELL REPORTS, 2014, 6 (05) :855-867
[52]   TNF-α and cancer cachexia: Molecular insights and clinical implications [J].
Patel, Hetal J. ;
Patel, Bhoomika M. .
LIFE SCIENCES, 2017, 170 :56-63
[53]   HUMAN-TUMOR NECROSIS FACTOR - PRECURSOR STRUCTURE, EXPRESSION AND HOMOLOGY TO LYMPHOTOXIN [J].
PENNICA, D ;
NEDWIN, GE ;
HAYFLICK, JS ;
SEEBURG, PH ;
DERYNCK, R ;
PALLADINO, MA ;
KOHR, WJ ;
AGGARWAL, BB ;
GOEDDEL, DV .
NATURE, 1984, 312 (5996) :724-729
[54]   Tumor-promoting function of apoptotic caspases by an amplification loop involving ROS, macrophages and JNK in Drosophila [J].
Perez, Ernesto ;
Lindblad, Jillian L. ;
Bergmann, Andreas .
ELIFE, 2017, 6
[55]   The function of TRADD in signaling through tumor necrosis factor receptor 1 and TRIF-dependent Toll-like receptors [J].
Pobezinskaya, Yelena L. ;
Kim, You-Sun ;
Choksi, Swati ;
Morgan, Michael J. ;
Li, Tao ;
Liu, Chengyu ;
Liu, Zhenggang .
NATURE IMMUNOLOGY, 2008, 9 (09) :1047-1054
[56]   The effects of reproduction on longevity and fertility in male Drosophila melanogaster [J].
Prowse, N ;
Partridge, L .
JOURNAL OF INSECT PHYSIOLOGY, 1997, 43 (06) :501-512
[57]   Eiger-induced cell death relies on Rac1-dependent endocytosis [J].
Ruan, W. ;
Srinivasan, A. ;
Lin, S. ;
Kara, K-I ;
Barker, P. A. .
CELL DEATH & DISEASE, 2016, 7 :e2181-e2181
[58]   Wengen, the Sole Tumour Necrosis Factor Receptor in Drosophila, Collaborates with Moesin to Control Photoreceptor Axon Targeting during Development [J].
Ruan, Wenjing ;
Unsain, Nicolas ;
Desbarats, Julie ;
Fon, Edward A. ;
Barker, Philip A. .
PLOS ONE, 2013, 8 (03)
[59]   Eiger/TNFα-mediated Dilp8 and ROS production coordinate intra-organ growth in Drosophila [J].
Sanchez, Juan A. ;
Mesquita, Duarte ;
Ingaramo, Maria C. ;
Ariel, Federico ;
Milan, Marco ;
Dekanty, Andres .
PLOS GENETICS, 2019, 15 (08)
[60]   Drosophila eiger mutants are sensitive to extracellular pathogens [J].
Schneider, David S. ;
Ayres, Janelle S. ;
Brandt, Stephanie M. ;
Costa, Alexandre ;
Dionne, Marc S. ;
Gordon, Michael D. ;
Mabery, Eric M. ;
Moule, Madeleine G. ;
Pham, Linh N. ;
Shirasu-Hiza, Mimi M. .
PLOS PATHOGENS, 2007, 3 (03)