spacer gif spacer gif spacer gif spacer gif ARCHIVE ANNOUNCEMENT! spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

doi: 10.1242/10.1242/dev.00467


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McLaughlin, T.
Right arrow Articles by O'Leary, D. D. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McLaughlin, T.
Right arrow Articles by O'Leary, D. D. M.
Development 130, 2407-2418 (2003)
Copyright © 2003 The Company of Biologists Limited

Bifunctional action of ephrin-B1 as a repellent and attractant to control bidirectional branch extension in dorsal-ventral retinotopic mapping

Todd McLaughlin, Robert Hindges, Paul A. Yates and Dennis D. M. O'Leary*

Molecular Neurobiology Laboratory, The Salk Institute, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA

* Author for correspondence (e-mail: doleary{at}salk.edu)

Accepted 3 March 2003

We report that the EphB receptor ligand, ephrin-B1, may act bifunctionally as both a branch repellent and attractant to control the unique mechanisms in mapping the dorsal-ventral (DV) retinal axis along the lateral-medial (LM) axis of the optic tectum. EphB receptors are expressed in a low to high DV gradient by retinal ganglion cells (RGCs), and ephrin-B1 is expressed in a low to high LM gradient in the tectum. RGC axons lack DV ordering along the LM tectal axis, but directionally extend interstitial branches that establish retinotopically ordered arbors. Recent studies show that ephrin-B1 acts as an attractant in DV mapping and in controlling directional branch extension. Modeling indicates that proper DV mapping requires that this attractant activity cooperates with a repellent activity in a gradient that mimics ephrin-B1. We show that ectopic domains of high, graded ephrin-B1 expression created by retroviral transfection repel interstitial branches of RGC axons and redirect their extension along the LM tectal axis, away from their proper termination zones (TZs). In contrast, the primary RGC axons are unaffected and extend through the ectopic domains of ephrin-B1 and arborize at the topographically correct site. However, when the location of a TZ is coincident with ectopic domains of ephrin-B1, the domains appear to inhibit arborization and shape the distribution of arbors. Our findings indicate that ephrin-B1 selectively controls, through either attraction or repulsion, the directional extension and arborization of interstitial branches extended by RGC axons arising from the same DV position: branches that arise from axons positioned lateral to the correct TZ are attracted up the gradient of ephrin-B1 and branches that arise from axons positioned medial to the same TZ are repelled down the ephrin-B1 gradient. Alternatively, EphB receptor signaling may act as a `ligand-density sensor' and titrate signaling pathways that promote branch extension toward an optimal ephrin-B1 concentration found at the TZ; branches located either medial or lateral to the TZ would encounter a gradient of increasingly favored attachment in the direction of the TZ.

Key words: Axon attraction, Axon branching, Axon guidance, Axon repellents, Chick visual system, Electroporation, Optic tectum, Eph receptors, Gradients, Recombinant retrovirus, Topographic maps




This article has been cited by other articles:


Home page
J. Neurosci.Home page
D. T. Plas, O. S. Dhande, J. E. Lopez, D. Murali, C. Thaller, M. Henkemeyer, Y. Furuta, P. Overbeek, and M. C. Crair
Bone Morphogenetic Proteins, Eye Patterning, and Retinocollicular Map Formation in the Mouse
J. Neurosci., July 9, 2008; 28(28): 7057 - 7067.
[Abstract] [Full Text] [PDF]


Home page
Sci SignalHome page
M. Lackmann and A. W. Boyd
Eph, a Protein Family Coming of Age: More Confusion, Insight, or Complexity?
Sci. Signal., April 15, 2008; 1(15): re2 - re2.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Buhusi, M. C. Schlatter, G. P. Demyanenko, R. Thresher, and P. F. Maness
L1 Interaction with Ankyrin Regulates Mediolateral Topography in the Retinocollicular Projection
J. Neurosci., January 2, 2008; 28(1): 177 - 188.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
T. A. Jones, P. A. Leake, R. L. Snyder, O. Stakhovskaya, and B. Bonham
Spontaneous Discharge Patterns in Cochlear Spiral Ganglion Cells Before the Onset of Hearing in Cats
J Neurophysiol, October 1, 2007; 98(4): 1898 - 1908.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
H. Sakuta, H. Takahashi, T. Shintani, K. Etani, A. Aoshima, and M. Noda
Role of bone morphogenic protein 2 in retinal patterning and retinotectal projection.
J. Neurosci., October 18, 2006; 26(42): 10868 - 10878.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
J. W. Kim and G. Lemke
Hedgehog-regulated localization of Vax2 controls eye development.
Genes & Dev., October 15, 2006; 20(20): 2833 - 2847.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
M. Boyle, A. Nighorn, and J. B. Thomas
Drosophila Eph receptor guides specific axon branches of mushroom body neurons
Development, May 1, 2006; 133(9): 1845 - 1854.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. Sen, S. Harpavat, M. A. Peters, and C. L. Cepko
Retinoic acid regulates the expression of dorsoventral topographic guidance molecules in the chick retina
Development, December 1, 2005; 132(23): 5147 - 5159.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
L. I. Brodsky, J. Jacob-Hirsch, A. Avivi, L. Trakhtenbrot, S. Zeligson, N. Amariglio, A. Paz, A. B. Korol, M. Band, G. Rechavi, et al.
Evolutionary regulation of the blind subterranean mole rat, Spalax, revealed by genome-wide gene expression
PNAS, November 22, 2005; 102(47): 17047 - 17052.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
H. Matsuoka, H. Obama, M. L. Kelly, T. Matsui, and M. Nakamoto
Biphasic Functions of the Kinase-defective Ephb6 Receptor in Cell Adhesion and Migration
J. Biol. Chem., August 12, 2005; 280(32): 29355 - 29363.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
N. Uesaka, S. Hirai, T. Maruyama, E. S. Ruthazer, and N. Yamamoto
Activity Dependence of Cortical Axon Branch Formation: A Morphological and Electrophysiological Study Using Organotypic Slice Cultures
J. Neurosci., January 5, 2005; 25(1): 1 - 9.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
T. Pratt, N. M. M.-L. Tian, T. I. Simpson, J. O. Mason, and D. J. Price
The winged helix transcription factor Foxg1 facilitates retinal ganglion cell axon crossing of the ventral midline in the mouse
Development, August 1, 2004; 131(15): 3773 - 3784.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. Eberhart, J. Barr, S. O'Connell, A. Flagg, M. E. Swartz, K. S. Cramer, K. W. Tosney, E. B. Pasquale, and C. E. Krull
Ephrin-A5 Exerts Positive or Inhibitory Effects on Distinct Subsets of EphA4-Positive Motor Neurons
J. Neurosci., February 4, 2004; 24(5): 1070 - 1078.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
Y. Liu, J. Berndt, F. Su, H. Tawarayama, W. Shoji, J. Y. Kuwada, and M. C. Halloran
Semaphorin3D Guides Retinal Axons along the Dorsoventral Axis of the Tectum
J. Neurosci., January 14, 2004; 24(2): 310 - 318.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
A. Palmer and R. Klein
Multiple roles of ephrins in morphogenesis, neuronal networking, and brain function
Genes & Dev., June 15, 2003; 17(12): 1429 - 1450.
[Full Text] [PDF]




© The Company of Biologists Ltd 2003