Astrocytes Play a Key Role in Drosophila Mushroom Body Axon Pruning

被引:61
作者
Hakim, Yaniv [1 ]
Yaniv, Shiri P. [1 ]
Schuldiner, Oren [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
基金
以色列科学基金会;
关键词
METAMORPHOSIS; RECEPTOR; DEGENERATION; EXPRESSION; DISEASE; PROTEIN; DRAPER; SYSTEM; BRAIN;
D O I
10.1371/journal.pone.0086178
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
Axon pruning is an evolutionarily conserved strategy used to remodel neuronal connections during development. The Drosophila mushroom body (MB) undergoes neuronal remodeling in a highly stereotypical and tightly regulated manner, however many open questions remain. Although it has been previously shown that glia instruct pruning by secreting a TGF-beta ligand, myoglianin, which primes MB neurons for fragmentation and also later engulf the axonal debris once fragmentation has been completed, which glia subtypes participate in these processes as well as the molecular details are unknown. Here we show that, unexpectedly, astrocytes are the major glial subtype that is responsible for the clearance of MB axon debris following fragmentation, even though they represent only a minority of glia in the MB area during remodeling. Furthermore, we show that astrocytes both promote fragmentation of MB axons as well as clear axonal debris and that this process is mediated by ecdysone signaling in the astrocytes themselves. In addition, we found that blocking the expression of the cell engulfment receptor Draper in astrocytes only affects axonal debris clearance. Thereby we uncoupled the function of astrocytes in promoting axon fragmentation to that of clearing axonal debris after fragmentation has been completed. Our study finds a novel role for astrocytes in the MB and suggests two separate pathways in which they affect developmental axon pruning.
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页数:12
相关论文
共 29 条
[1]   Essential role of the apoptotic cell engulfment genes draper and ced-6 in programmed axon pruning during Drosophila metamorphosis [J].
Awasaki, T ;
Tatsumi, R ;
Takahashi, K ;
Arai, K ;
Nakanishi, Y ;
Ueda, R ;
Ito, K .
NEURON, 2006, 50 (06) :855-867
[2]   Engulfing action of glial cells is required for programmed axon pruning during Drosophila metamorphosis [J].
Awasaki, T ;
Ito, K .
CURRENT BIOLOGY, 2004, 14 (08) :668-677
[3]   Glia instruct developmental neuronal remodeling through TGF-β signaling [J].
Awasaki, Takeshi ;
Huang, Yaling ;
O'Connor, Michael B. ;
Lee, Tzumin .
NATURE NEUROSCIENCE, 2011, 14 (07) :821-823
[4]  
Boulanger A, 2010, NAT NEUROSCI
[5]   RETRACTED: Alteration of astrocytes and Wnt/β-catenin signaling in the frontal cortex of autistic subjects (Retracted article. See vol. 13, 106, 2016) [J].
Cao, Fujiang ;
Yin, Ailan ;
Wen, Guang ;
Sheikh, Ashfaq M. ;
Tauqeer, Zujaja ;
Malik, Mazhar ;
Nagori, Amenah ;
Schirripa, Michael ;
Schirripa, Frank ;
Merz, George ;
Brown, W. Ted ;
Li, Xiaohong .
JOURNAL OF NEUROINFLAMMATION, 2012, 9
[6]   Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways [J].
Chung, Won-Suk ;
Clarke, Laura E. ;
Wang, Gordon X. ;
Stafford, Benjamin K. ;
Sher, Alexander ;
Chakraborty, Chandrani ;
Joung, Julia ;
Foo, Lynette C. ;
Thompson, Andrew ;
Chen, Chinfei ;
Smith, Stephen J. ;
Barres, Ben A. .
NATURE, 2013, 504 (7480) :394-+
[7]   Architects in neural circuit design: Glia control neuron numbers and connectivity [J].
Cody, Megan M. ;
Freeman, Marc R. .
JOURNAL OF CELL BIOLOGY, 2013, 203 (03) :395-405
[8]   Ensheathing Glia Function as Phagocytes in the Adult Drosophila Brain [J].
Doherty, Johnna ;
Logan, Mary A. ;
Tasdemir, Oezge E. ;
Freeman, Marc R. .
JOURNAL OF NEUROSCIENCE, 2009, 29 (15) :4768-4781
[9]   Glia and Muscle Sculpt Neuromuscular Arbors by Engulfing Destabilized Synaptic Boutons and Shed Presynaptic Debris [J].
Fuentes-Medel, Yuly ;
Logan, Mary A. ;
Ashley, James ;
Ataman, Bulent ;
Budnik, Vivian ;
Freeman, Marc R. .
PLOS BIOLOGY, 2009, 7 (08)
[10]   Retinal axon target selection in Drosophila is regulated by a receptor protein tyrosine phosphatase [J].
Garrity, PA ;
Lee, CH ;
Salecker, I ;
Robertson, HC ;
Desai, CJ ;
Zinn, K ;
Zipursky, SL .
NEURON, 1999, 22 (04) :707-717