Development of normal and injury-induced gene expression of aFGF, bFGF, CNTF, BDNF, GFAP and IGF-I in the rat retina

被引:104
作者
Cao, W
Li, F
Steinberg, RH
Lavail, MM
机构
[1] Univ Oklahoma, Dept Ophthalmol, Dean A McGee Eye Inst, Oklahoma City, OK 73104 USA
[2] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
关键词
basic fibroblast growth factor; acidic fibroblast growth factor; fibroblast growth factor receptor-1; ciliary neurotrophic factor; brain-derived neurotrophic factor; insulin-like growth factor-I; glial fibrillary acidic protein; injury; rat; retina; development;
D O I
10.1006/exer.2001.0990
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Focal mechanical injury to the retina substantially increases basic fibroblast growth factor (bFGF) and ciliary neurotrophic factor (CNTF) mRNA expression, accompanied by a transient increase in FGFR-1 mRNA, and this response is thought to protect photoreceptors near the injury site from inherited and light-induced retinal degenerations. We have now examined retinal gene expression of the principal survival factors involved in the response to injury in normal rats as a function of postnatal age both in normal and injured retinas. Sprague-Dawley rats were injured in one eye by needle incision through the retina at postnatal day (P) 10, 23, 35, 60, 90, 120 and 180. The other eye was uninjured and served as the control. Retinas were taken 1 day post-injury. Northern blot analysis was performed to determine the mRNA expression of the following factors and receptors: bFGF and acidic fibroblast growth factors (aFGF) and FGF receptor-1 (FGFR-1); CNTF and CNTF receptor alpha (CNTFR-alpha); brain-derived neurotrophic factor (BDNF) and its receptor trkB; and insulin-like growth factor-I (IGF-I) and IGF-I receptor (IGF-IR); glial fibrillary acidic protein (GFAP) and opsin, In the uninjured control eyes, mRNA expression of most of the factors increased with, postnatal age, with little expression at P10 and maximal expression levels reached at P21 (opsin), P35 (aFGF), P60 (BDNF) or P90 (bFGF, FGFR-1, CNTF and GFAP). In contrast, IGF-1 mRNA rapidly decreased from a high level of expression at P10 to about 55 % of that level by P22, reaching a stable 45-50 % of the P10 level at P35 and thereafter. The response to injury of bFGF, FGFR-1, CNTF and GFAP mRNAs increased with postnatal age. Unexpectedly, only minimal increases in bFGF, FGFR-1, CNTF and GFAP over those seen in the control eyes were observed before P35. Thereafter. the increase of bFGF mRNA after injury reached a maximum of three-fold at P60, maintained this level to P120, and slightly decreased to 2.5-fold by P180. Expression of FGFR-1 mRNA showed a maximum increase of 2.6-fold at P90. Expression of CNTF and GFAP mRNAs followed a time course similar to that of bFGF. Mechanical injury did not alter the mRNA levels of aFGF, BDNF, IGF-I, and receptors, CNTFR-alpha, trkB and IGF-IR. These data show that the response to injury is minimal at early postnatal ages but increases with age and peaks at P60-90 for most potential survival factors. (C) 2001 Academic Press.
引用
收藏
页码:591 / 604
页数:14
相关论文
共 53 条
[31]   DISTRIBUTION AND REGULATION OF RAT INSULIN-LIKE GROWTH FACTOR-I MESSENGER RIBONUCLEIC-ACIDS ENCODING ALTERNATIVE CARBOXYTERMINAL E-PEPTIDES - EVIDENCE FOR DIFFERENTIAL PROCESSING AND REGULATION IN LIVER [J].
LOWE, WL ;
LASKY, SR ;
LEROITH, D ;
ROBERTS, CT .
MOLECULAR ENDOCRINOLOGY, 1988, 2 (06) :528-535
[32]  
LUO L, 1993, HEARING RES, V69, P182
[33]   REGULATION OF CELL-DIVISION AND ROD DIFFERENTIATION IN THE TELEOST RETINA [J].
MACK, AF ;
FERNALD, RD .
DEVELOPMENTAL BRAIN RESEARCH, 1993, 76 (02) :183-187
[34]   NT-3, BDNF, AND NGF IN THE DEVELOPING RAT NERVOUS-SYSTEM - PARALLEL AS WELL AS RECIPROCAL PATTERNS OF EXPRESSION [J].
MAISONPIERRE, PC ;
BELLUSCIO, L ;
FRIEDMAN, B ;
ALDERSON, RF ;
WIEGAND, SJ ;
FURTH, ME ;
LINDSAY, RM ;
YANCOPOULOS, GD .
NEURON, 1990, 5 (04) :501-509
[35]   EXPRESSION PATTERN OF ACIDIC AND BASIC FIBROBLAST GROWTH-FACTOR GENES IN ADULT-RAT EYES [J].
NOJI, S ;
MATSUO, T ;
KOYAMA, E ;
YAMAAI, T ;
NOHNO, T ;
MATSUO, N ;
TANIGUCHI, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 168 (01) :343-349
[36]  
OHTA M, 1996, BIOCHEM MOL BIOL INT, V35, P283
[37]   GROWTH FACTOR-INDUCED RETINAL REGENERATION IN-VIVO [J].
PARK, CM ;
HOLLENBERG, MJ .
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL 146, 1993, 146 :49-74
[38]  
Pittack C, 1997, DEVELOPMENT, V124, P805
[39]   IMMUNOLOCALIZATION OF BASIC FIBROBLAST GROWTH-FACTOR AND ITS RECEPTOR IN ADULT GOLDFISH RETINA [J].
RAYMOND, PA ;
BARTHEL, LK ;
ROUNSIFER, ME .
EXPERIMENTAL NEUROLOGY, 1992, 115 (01) :73-78
[40]  
Reh TA, 1998, J NEUROBIOL, V36, P206, DOI 10.1002/(SICI)1097-4695(199808)36:2<206::AID-NEU8>3.0.CO