DSCAMs: restoring balance to developmental forces

被引:23
作者
Garrett, Andrew M. [1 ]
Tadenev, Abigail L. D. [1 ]
Burgess, Robert W. [1 ]
机构
[1] Jackson Lab, Bar Harbor, ME 04609 USA
来源
FRONTIERS IN MOLECULAR NEUROSCIENCE | 2012年 / 5卷
关键词
DSCAM; Dscaml1; cell adhesion; chemoattraction; retina; self-avoidance; chemorepulsion; CELL-ADHESION MOLECULES; LEECH HAEMENTERIA-GHILIANII; DROSOPHILA SENSORY NEURONS; DENDRITIC SELF-AVOIDANCE; AXON GUIDANCE; NETRIN RECEPTOR; MORPHOGENESIS; ARBORIZATION; ATTRACTION; MORPHOLOGY;
D O I
10.3389/fnmol.2012.00086
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Many of the models of neurodevelopmental processes such as cell migration, axon outgrowth, and dendrite arborization involve cell adhesion and chemoattraction as critical physical or mechanical aspects of the mechanism. However, the prevention of adhesion or attraction is under-appreciated as a necessary, active process that balances these forces, insuring that the correct cells are present and adhering in the correct place at the correct time. The phenomenon of not adhering is often viewed as the passive alternative to adhesion, and in some cases this may be true. However, it is becoming increasingly clear that active signaling pathways are involved in preventing adhesion. These provide a balancing force during development that prevents overly exuberant adhesion, which would otherwise disrupt normal cellular and tissue morphogenesis. The strength of chemoattractive signals may be similarly modulated. Recent studies, described here, suggest that Down Syndrome Cell Adhesion Molecule (DSCAM), and closely related proteins such as DSCAML1, may play an important developmental role as such balancers in multiple systems.
引用
收藏
页数:7
相关论文
共 50 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]   Down syndrome cell adhesion molecule DSCAM mediates homophilic intercellular adhesion [J].
Agarwala, KL ;
Nakamura, S ;
Tsutsumi, Y ;
Yamakawa, K .
MOLECULAR BRAIN RESEARCH, 2000, 79 (1-2) :118-126
[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 Down Syndrome Critical Region Regulates Retinogeniculate Refinement [J].
Blank, Martina ;
Fuerst, Peter G. ;
Stevens, Beth ;
Nouri, Navid ;
Kirkby, Lowry ;
Warrier, Deepti ;
Barres, Ben A. ;
Feller, Marla B. ;
Huberman, Andrew D. ;
Burgess, Robert W. ;
Garner, Craig C. .
JOURNAL OF NEUROSCIENCE, 2011, 31 (15) :5764-5776
[5]   Adhesion molecule signalling: not always a sticky business [J].
Cavallaro, Ugo ;
Dejana, Elisabetta .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2011, 12 (03) :189-197
[6]   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
[7]   Cell autonomy of DSCAM function in retinal development [J].
Fuerst, Peter G. ;
Bruce, Freyja ;
Rounds, Ryan P. ;
Erskine, Lynda ;
Burgess, Robert W. .
DEVELOPMENTAL BIOLOGY, 2012, 361 (02) :326-337
[8]   A Novel Null Allele of Mouse Dscam Survives to Adulthood on an Inbred C3H Background With Reduced Phenotypic Variability [J].
Fuerst, Peter G. ;
Harris, Belinda S. ;
Johnson, Kenneth R. ;
Burgess, Robert W. .
GENESIS, 2010, 48 (10) :578-584
[9]   DSCAM and DSCAML1 Function in Self-Avoidance in Multiple Cell Types in the Developing Mouse Retina [J].
Fuerst, Peter G. ;
Bruce, Freyja ;
Tian, Miao ;
Wei, Wei ;
Elstrott, Justin ;
Feller, Maria B. ;
Erskine, Lynda ;
Singer, Joshua H. ;
Burgess, Robert W. .
NEURON, 2009, 64 (04) :484-497
[10]   Adhesion molecules in establishing retinal circuitry [J].
Fuerst, Peter G. ;
Burgess, Robert W. .
CURRENT OPINION IN NEUROBIOLOGY, 2009, 19 (04) :389-394