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PMID: 7541558 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Disruption of retinal axon ingrowth by ablation of embryonic mouse optic chiasm neurons.

Science (New York, N.Y.) ·Vol. 269 ·No. 5220 ·1995-07-07 ·Pages 98-101

Sretavan DW, Puré E, Siegel MW, Reichardt LF

Abstract

Mouse retinal ganglion cell axons growing from the eye encounter embryonic neurons at the future site of the optic chiasm. After in vivo ablation of these chiasm neurons with a monoclonal antibody and complement, retinal axons did not cross the midline and stalled at approximately the entry site into the chiasm region. Thus, in the mouse, the presence of early-generated neurons that reside at the site of the future chiasm is required for formation of the optic chiasm by retinal ganglion cell axons.

MeSH Terms
Animals Antibodies, Monoclonal Axons/physiology,ultrastructure Carrier Proteins/immunology Hyaluronan Receptors Hypothalamus/cytology,embryology Mice Mice, Inbred C57BL Neurons/physiology,ultrastructure Optic Chiasm/cytology,embryology Optic Nerve/embryology Receptors, Cell Surface/immunology Receptors, Lymphocyte Homing/immunology Retina/embryology Retinal Ganglion Cells/physiology Visual Pathways/embryology
Chemicals
Antibodies, Monoclonal Carrier Proteins Hyaluronan Receptors Receptors, Cell Surface Receptors, Lymphocyte Homing
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sretavan D W
Department of Ophthalmology, University of California, San Francisco 94143, USA.
Puré E
Siegel M W
Reichardt L F
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1995-07-07
Pages
98-101
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NEI NIH HHS · EY10688 · United States
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