DSCAM and DSCAML1 Function in Self-Avoidance in Multiple Cell Types in the Developing Mouse Retina

被引:188
作者
Fuerst, Peter G. [1 ]
Bruce, Freyja [2 ]
Tian, Miao [3 ]
Wei, Wei [5 ]
Elstrott, Justin [5 ]
Feller, Maria B. [5 ]
Erskine, Lynda [2 ]
Singer, Joshua H. [3 ,4 ]
Burgess, Robert W. [1 ]
机构
[1] Jackson Lab, Bar Harbor, ME 04609 USA
[2] Univ Aberdeen, Sch Med Sci, Aberdeen AB25 2ZD, Scotland
[3] Northwestern Univ, Feinberg Sch Med, Dept Ophthalmol, Chicago, IL 60611 USA
[4] Northwestern Univ, Feinberg Sch Med, Dept Physiol, Chicago, IL 60611 USA
[5] Univ Calif Berkeley, Dept Mol Cell Biol, Berkeley, CA 94720 USA
基金
英国生物技术与生命科学研究理事会; 美国国家卫生研究院;
关键词
AXON GUIDANCE; DROSOPHILA DSCAM; ADHESION MOLECULE; NETRIN RECEPTOR; DIVERSITY; RECOGNITION; EXPRESSION; NEURONS; SYNAPSE; GENES;
D O I
10.1016/j.neuron.2009.09.027
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
DSCAM and DSCAM-LIKE1 (DSCAML1) serve diverse neurodevelopmental functions, including axon guidance, synaptic adhesion, and self-avoidance, depending on the species, cell type, and gene family member studied. We examined the function of DSCAM and DSCAML1 in the developing mouse retina. In addition to a subset of amacrine cells, Dscaml1 was expressed in most retinal ganglion cells (RGCs). RGCs had fasciculated dendrites and clumped cell bodies in Dscam(-/-) mice, suggesting a role in self-avoidance. Dscaml1 was expressed in the rod circuit, and mice lacking Dscaml1 had fasciculated rod bipolar cell dendrites and clumped All amacrine cell bodies, also indicating a role in self-avoidance. Neurons in Dscam or Dscaml1 mutant retinas stratified their processes appropriately in synaptic laminae in the inner plexiform layer, and functional synapses formed in the rod circuit in mice lacking Dscaml1. Therefore, DSCAM and DSCAML1 function similarly in self-avoidance, and are not essential for synaptic specificity in the mouse retina.
引用
收藏
页码:484 / 497
页数:14
相关论文
共 47 条
[1]   Cloning and functional characterization of DSCAML1, a novel DSCAM-like cell adhesion molecule that mediates homophilic intercellular adhesion [J].
Agarwala, KL ;
Ganesh, S ;
Tsutsumi, Y ;
Suzuki, T ;
Amano, K ;
Yamakawa, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 285 (03) :760-772
[2]   DSCAM Deficiency Causes Loss of Pre-Inspiratory Neuron Synchroneity and Perinatal Death [J].
Amano, Kenji ;
Fujii, Morimitsu ;
Arata, Satoru ;
Tojima, Takuro ;
Ogawa, Masaharu ;
Morita, Noriyuki ;
Shimohata, Atsushi ;
Furuichi, Teiichi ;
Itohara, Shigeyoshi ;
Kamiguchi, Hiroyuki ;
Korenberg, Julie R. ;
Arata, Akiko ;
Yamakawa, Kazuhiro .
JOURNAL OF NEUROSCIENCE, 2009, 29 (09) :2984-2996
[3]   Dscam guides embryonic axons by Netrin-dependent and -independent functions [J].
Andrews, Gracie L. ;
Tanglao, Shawna ;
Farmer, W. Todd ;
Morin, Steves ;
Brotman, Steven ;
Berberoglu, Michael A. ;
Price, Hilary ;
Fernandez, George C. ;
Mastick, Grant S. ;
Charron, Frederic ;
Kidd, Thomas .
DEVELOPMENT, 2008, 135 (23) :3839-3848
[4]   The molecular diversity of Dscam is functionally required for neuronal wiring specificity in Drosophila [J].
Chen, Brian E. ;
Kondo, Masahiro ;
Garnier, Amélie ;
Watson, Fiona L. ;
Puettmann-Holgado, Roland ;
Lamar, David R. ;
Schmucker, Dietmar .
CELL, 2006, 125 (03) :607-620
[5]   Morphological properties of mouse retinal ganglion cells [J].
Coombs, J. ;
van der List, D. ;
Wang, G. -Y. ;
Chalupa, L. M. .
NEUROSCIENCE, 2006, 140 (01) :123-136
[6]  
Erskine L, 2000, J NEUROSCI, V20, P4975
[7]   Neurite arborization and mosaic spacing in the mouse retina require DSCAM [J].
Fuerst, Peter G. ;
Koizumi, Amane ;
Masland, Richard H. ;
Burgess, Robert W. .
NATURE, 2008, 451 (7177) :470-U8
[8]   Defects in eye development in transgenic mice overexpressing the heparan sulfate proteoglycan agrin [J].
Fuerst, Peter G. ;
Rauch, Steven M. ;
Burgess, Robert W. .
DEVELOPMENTAL BIOLOGY, 2007, 303 (01) :165-180
[9]   The genesis of retinal architecture: An emerging role for mechanical interactions? [J].
Galli-Resta, Lucia ;
Leone, Paola ;
Bottari, David ;
Ensini, Monica ;
Rigosi, Elisa ;
Novelli, Elena .
PROGRESS IN RETINAL AND EYE RESEARCH, 2008, 27 (03) :260-283
[10]   Mapping of genetic modifiers of Nr2e3rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity [J].
Haider, Neena B. ;
Zhang, Weidong ;
Hurd, Ron ;
Ikeda, Akihiro ;
Nystuen, Arne M. ;
Naggert, Ju R. Rgen K. ;
Nishina, Patsy M. .
MAMMALIAN GENOME, 2008, 19 (03) :145-154