TIMP-3 IS EXPRESSED IN THE HUMAN RETINAL-PIGMENT EPITHELIUM

Authors
Citation
A. Ruiz et al., TIMP-3 IS EXPRESSED IN THE HUMAN RETINAL-PIGMENT EPITHELIUM, Biochemical and biophysical research communications, 226(2), 1996, pp. 467-474
Citations number
34
Categorie Soggetti
Biology,Biophysics
ISSN journal
0006291X
Volume
226
Issue
2
Year of publication
1996
Pages
467 - 474
Database
ISI
SICI code
0006-291X(1996)226:2<467:TIEITH>2.0.ZU;2-I
Abstract
TIMP-3 is the most recent member of the tissue inhibitor of metallopro teinases (TIMP) family. In the present study, we describe the expressi on of TIMP-3 messenger RNA (mRNA) by the retinal pigment epithelium of the normal human eye (hRPE). In addition to the three predominant tra nscripts of approximately 5.1, 2.8, and 2.4 Kbp found in several other human tissues at adult and fetal stages. The hRPE also expresses two RNA species of 1.2 and 1.0 Kbp. Based on the sequence analysis of cDNA clones isolated from a hRPE cDNA library, the use of alternate polyad enylation signals could account for the expression of these smaller tr anscripts. The possibility of an alternative mechanism of regulation o f the expression of TIMP-3 by the RPE is not discarded. The number of RNA transcripts specific for TIMP-3 per nanogram of poly A(+) RNA was quantified by RT-PCR. 9.6x10(5) transcripts per nanogram of polyA (+)R NA were found at the adult stage and 1.2X10(6) transcripts per nanogra m of polyA (+)RNA were detected at the fetal stage. These findings wer e supported by the predominant labeling in the RPE layer of retinal ti ssue sections in in situ hybridization experiments. All of these data support the hypothesis that the production of TIMP-3 by the RPE may be crucial for the maintenance of Bruch's membrane, the complex layer of extracellular matrix that provides a structural substrate for the RPE in the healthy retina and is perturbed during the ageing process and in Sorby's Fundus Dystrophy, a dominantly inherited disease. (C) 1996 Academic Press, Inc.