IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


(Investigative Ophthalmology and Visual Science. 2007;48:2304-2310.)
© 2007 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.06-0486

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
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 ISI Web of Science (6)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bernstein, S. L.
Right arrow Articles by Kelman, S. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bernstein, S. L.
Right arrow Articles by Kelman, S. E.

Neuron Stress and Loss Following Rodent Anterior Ischemic Optic Neuropathy in Double-Reporter Transgenic Mice

Steven L. Bernstein,1,2 Yan Guo,1 Bernard J. Slater,1 Adam Puche,2 and Shalom E. Kelman1

1From the Departments of Ophthalmology and 2Anatomy and Neurobiology, University of Maryland at Baltimore, School of Medicine, Baltimore, Maryland.

PURPOSE. Nonarteritic anterior ischemic optic neuropathy (NAION) is an optic nerve infarct involving axons of retinal ganglion cell (RGC) neurons. The rodent NAION model (rAION) can use transgenic mouse strains to reveal unique characteristics about the effects of sudden optic nerve ischemia on RGCs and their axons. The impact of rAION on RGC stress patterns, RGC loss, and their axons after axonal infarct were evaluated.

METHODS. A double-transgenic mouse strain was used, containing a construct with cyan fluorescent protein (CFP) under Thy-1 promoter control, and a construct with ß-galactosidase (lacZ) linked to the stress gene c-fos promoter. Thy-1 in the retina is expressed predominantly in RGCs, enabling stereologic analysis of CFP(+) RGC numbers and loss post-rAION-using confocal microscopy. RGC loss was correlated with axonal counts using transmission electron microscopy (TEM). LacZ immunohistochemistry was used to evaluate retinal cell stress after rAION.

RESULTS. The 45,000 CFP(+) cells in the RGC layer of control animals compared with previous RGC quantitative estimates. rAION produced RGC stress, defined as lacZ expression, in patterns corresponding with later RGC loss. rAION-associated RGC loss correlated with regional nerve fiber layer loss. Axonal loss correlates with stereologically determined RGC loss estimates in transgenic mice retinas.

CONCLUSIONS. Post-ON infarct RGC stress patterns correlate with regional RGC loss. Cellular lacZ levels in most RGCs are low, suggesting rAION-affected RGCs express c-fos only transiently. CFP(+) cell loss correlates closely with quantitative axonal loss, suggesting that the Thy-1 (CFP) transgenic mouse strain is appropriate for RGC stereologic analyses.





This article has been cited by other articles:


Home page
IOVSHome page
B. J. Slater, Z. Mehrabian, Y. Guo, A. Hunter, and S. L. Bernstein
Rodent Anterior Ischemic Optic Neuropathy (rAION) Induces Regional Retinal Ganglion Cell Apoptosis with a Unique Temporal Pattern
Invest. Ophthalmol. Vis. Sci., August 1, 2008; 49(8): 3671 - 3676.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the Association for Research in Vision and Ophthalmology