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


     


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 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 Hitchcock, P. F.
Right arrow Articles by Cirenza, P. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hitchcock, P. F.
Right arrow Articles by Cirenza, P. F.
(Investigative Ophthalmology and Visual Science. 2001;42:2125-2129.)
© 2001 by The Association for Research in Vision and Ophthalmology, Inc.

Expression of the Insulin Receptor in the Retina of the Goldfish

Peter F. Hitchcock1, Deborah C. Otteson2 and Paul F. Cirenza1

1 From the Departments of Ophthalmology and Visual Sciences and Cell and Developmental Biology, The University of Michigan, Ann Arbor, Michigan; and 2 Wilmer Eye Institute, Baltimore, Maryland.

PURPOSE. Insulin is a peptide growth factor that is active in most tissues, both during development and in adulthood. The action of insulin is through its specific membrane receptor. Previously retinal progenitors in the adult goldfish were shown to proliferate vigorously when exposed to insulin in vitro.1 The present study was undertaken to clone and characterize partial cDNAs that encode the goldfish’s insulin receptor (IR) and to establish the cellular pattern of expression of this gene in the retina.

METHODS. Standard methods were used for RNA isolation, reverse transcription–polymerase chain reaction, Northern blot analysis, and in situ hybridization.

RESULTS. Multiple clones were isolated that, based on sequence analysis, segregated into two groups, presumed to represent two genes that encode the IR. These clones were designated goldfish IR-1 (gfIR-1) and goldfish IR-2 (gfIR-2). Northern blot analysis showed that both genes are expressed in multiple tissues, including the retina. Both gfIR-1 and -2 give rise to a single, major transcript, but the sizes of the two transcripts are different. In situ hybridizations using digoxygenin-labeled riboprobes showed that gfIR-1 and -2 are expressed by all differentiated retinal neurons as well as neuronal progenitors in the circumferential germinal zone.

CONCLUSIONS. These data demonstrate that the IR is expressed in the retina of the goldfish, and, on the basis of the cellular pattern of expression, suggest that insulin may act both to regulate neurogenesis and influence the function of differentiated neurons. The cellular coexpression of the receptors for both insulin-like growth factor (IGF) 1 and insulin suggests that neurons and/or neuronal progenitors in the retina of the goldfish may contain hybrid IGF-1/insulin receptors.




This article has been cited by other articles:


Home page
IOVSHome page
M. N. A. Mandal, V. Vasireddy, G. B. Reddy, X. Wang, S. E. Moroi, B. R. Pattnaik, B. A. Hughes, J. R. Heckenlively, P. F. Hitchcock, M. M. Jablonski, et al.
CTRP5 Is a Membrane-Associated and Secretory Protein in the RPE and Ciliary Body and the S163R Mutation of CTRP5 Impairs Its Secretion
Invest. Ophthalmol. Vis. Sci., December 1, 2006; 47(12): 5505 - 5513.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
R. Ayyagari, M. N. A. Mandal, A. J. Karoukis, L. Chen, N. C. McLaren, M. Lichter, D. T. Wong, P. F. Hitchcock, R. C. Caruso, S. E. Moroi, et al.
Late-Onset Macular Degeneration and Long Anterior Lens Zonules Result from a CTRP5 Gene Mutation
Invest. Ophthalmol. Vis. Sci., September 1, 2005; 46(9): 3363 - 3371.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2001 by the Association for Research in Vision and Ophthalmology