TRANSFORMING GROWTH-FACTOR-BETA-2 IS THE PREDOMINANT ISOFORM IN THE NEURAL RETINA, RETINAL-PIGMENT EPITHELIUM-CHOROID AND VITREOUS OF THE MONKEY EYE

被引:127
作者
PFEFFER, BA
FLANDERS, KC
GUERIN, CJ
DANIELPOUR, D
ANDERSON, DH
机构
[1] NEI, RETINAL CELL & MOLEC BIOL LAB, BETHESDA, MD 20892 USA
[2] NCI, CHEMOPREVENT LAB, BETHESDA, MD 20892 USA
[3] UNIV CALIF SANTA BARBARA, INST NEUROSCI, SANTA BARBARA, CA 93106 USA
关键词
TRANSFORMING GROWTH FACTOR BETA; RETINAL PIGMENT EPITHELIUM; PHOTORECEPTOR; MONKEY; IMMUNOCYTOCHEMISTRY; EPITHELIAL CELL CULTURE;
D O I
10.1006/exer.1994.1114
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Several techniques were utilized to assess the levels, disposition and cellular sources of isoforms 1 and 2 of transforming growth factor beta (TGF-beta) in the posterior pole of the monkey eye. Freshly dissected tissues, as well as the saline vehicles in which dissections were performed, were analysed by sandwich enzyme-linked immunosorbent assay. In all tissues TGF-beta 2 was the predominant isoform, with beta 2:beta 1 ratios of 6:1 for neural retina (as ng g(-1)) and 425:1 for vitreous (as pmol l(-1)). Retinal pigment epithelium (RPE)-Bruch's membrane-choroid complex contained approximately 10 times the amount of both TGF-beta isoforms as neural retina. For first passage cultures of monkey RPE, TGF-beta 2, but not TGF-beta 1, accumulated over time in conditioned media samples. Immunoreactivity for TGF-beta 2 was detected both in tissue sections of posterior pole, specifically in rod outer segments and RPE, and also in the first passage cultures of RPE. Antibodies to specific peptide sequences of both isoforms localized TGF-beta to the outer segments of rod photoreceptors. The apparent sequestration of TGF-beta 2 in photoreceptor outer segments, as well as the in vitro evidence for possible synthesis and release by RPE, suggest that TGF-beta 2 is an important modulator of visual function acting at the retina-RPE interface.
引用
收藏
页码:323 / 333
页数:11
相关论文
共 51 条
[41]   IDENTIFICATION OF A STRUCTURAL DOMAIN THAT DISTINGUISHES THE ACTIONS OF THE TYPE-1 AND TYPE-2 ISOFORMS OF TRANSFORMING GROWTH-FACTOR-BETA ON ENDOTHELIAL-CELLS [J].
QIAN, SW ;
BURMESTER, JK ;
MERWIN, JR ;
MADRI, JA ;
SPORN, MB ;
ROBERTS, AB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6290-6294
[43]   TRANSFORMING GROWTH-FACTORS - ISOLATION OF POLYPEPTIDES FROM VIRALLY AND CHEMICALLY TRANSFORMED-CELLS BY ACID-ETHANOL EXTRACTION [J].
ROBERTS, AB ;
LAMB, LC ;
NEWTON, DL ;
SPORN, MB ;
DELARCO, JE ;
TODARO, GJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (06) :3494-3498
[44]   TRANSCRIPTIONAL CONTROL OF EXPRESSION OF THE TGF-BETA-S [J].
ROBERTS, AB ;
KIM, SJ ;
KONDAIAH, P ;
JAKOWLEW, SB ;
DENHEZ, F ;
GLICK, AB ;
GEISER, AG ;
WATANABE, S ;
NOMA, T ;
LECHLEIDER, R ;
SPORN, MB .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1990, 593 :43-50
[45]   CELL TYPE SPECIFICITY OF TGF-BETA BINDING [J].
SEGARINI, PR .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1990, 593 :73-90
[46]   REVERSIBLE INHIBITION OF MAMMARY-GLAND GROWTH BY TRANSFORMING GROWTH-FACTOR-BETA [J].
SILBERSTEIN, GB ;
DANIEL, CW .
SCIENCE, 1987, 237 (4812) :291-293
[47]  
TANIHARA H, 1993, INVEST OPHTH VIS SCI, V34, P413
[48]   GROWTH INHIBITOR FROM BSC-1 CELLS CLOSELY RELATED TO PLATELET TYPE-BETA TRANSFORMING GROWTH-FACTOR [J].
TUCKER, RF ;
SHIPLEY, GD ;
MOSES, HL ;
HOLLEY, RW .
SCIENCE, 1984, 226 (4675) :705-707
[49]  
WAKEFIELD LM, 1988, J BIOL CHEM, V263, P7646
[50]   MONKEY RETINAL-PIGMENT EPITHELIAL-CELLS INVITRO SYNTHESIZE, SECRETE, AND DEGRADE INSULIN-LIKE GROWTH-FACTOR BINDING-PROTEINS [J].
WALDBILLIG, RJ ;
SCHOEN, TJ ;
CHADER, GJ ;
PFEFFER, BA .
JOURNAL OF CELLULAR PHYSIOLOGY, 1992, 150 (01) :76-83