Basic Fibroblast Growth Factor (FGF) in the Central Nervous System: Identification of Specific Loci of Basic FGF Expression in the Rat Brain

被引:224
作者
Emoto, Naoya [1 ]
Gonzalez, Ana-Maria [1 ]
Walicke, Patricia A. [2 ]
Wada, Etsuko [3 ]
Simmons, Donna M. [3 ]
Shimasaki, Shunichi [1 ]
Baird, Andrew
机构
[1] Whittier Inst Diabet & Endocrinol, Dept Mol & Cellular Growth Biol, 9894 Genesee, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Dept Neurosci, M-008, La Jolla, CA 92033 USA
[3] Salk Inst Biol Studies, Neural Syst Lab, La Jolla, CA 92037 USA
关键词
angiogenesis; hippocampus; in situ hybridization; neurotrophic factor;
D O I
10.3109/08977198909069078
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The expression of basic FGF mRNA, while virtually absent in peripheral tissues, appears to be constitutively expressed in the central nervous system. As such, while it is difficult to detect any mRNA encoding basic FGF in the heart, lung, kidneys, ovaries, liver, or pituitary of rats, the levels are easily detected in brain. A regional analysis of the expression of basic FGF mRNA in brain reveals that it is widely distributed in the cortex (frontal, parietal, and occipital), the hippocampus, hypothalamus, and pons. Only a few loci of basic FGF synthesis are detected by in situ hybridization and include layers 2 and 6 of the medial (cingulate) cortex, the indusium griseum, fasciola cinereum, and field CA2 of the hippocampus. The identification of specific cell populations in the brain, and particularly in the hippocampus, that synthesize basic FGF supports the notion that this potent neurotrophic factor is involved in normal CNS function and that the presence (or absence) of its expression may be linked to the pathogenesis of the neurogenerative diseases characterizing these various loci. The significance of these findings with respect to the regulation of basic FGF expression in peripheral tissue and the central nervous system is discussed.
引用
收藏
页码:21 / 29
页数:9
相关论文
共 30 条
[1]   NUCLEOTIDE-SEQUENCE OF A BOVINE CLONE ENCODING THE ANGIOGENIC PROTEIN, BASIC FIBROBLAST GROWTH-FACTOR [J].
ABRAHAM, JA ;
MERGIA, A ;
WHANG, JL ;
TUMOLO, A ;
FRIEDMAN, J ;
HJERRILD, KA ;
GOSPODAROWICZ, D ;
FIDDES, JC .
SCIENCE, 1986, 233 (4763) :545-548
[2]   HUMAN BASIC FIBROBLAST GROWTH-FACTOR - NUCLEOTIDE-SEQUENCE AND GENOMIC ORGANIZATION [J].
ABRAHAM, JA ;
WHANG, JL ;
TUMOLO, A ;
MERGIA, A ;
FRIEDMAN, J ;
GOSPODAROWICZ, D ;
FIDDES, JC .
EMBO JOURNAL, 1986, 5 (10) :2523-2528
[3]   BASIC FIBROBLAST GROWTH-FACTOR PREVENTS DEATH OF LESIONED CHOLINERGIC NEURONS INVIVO [J].
ANDERSON, KJ ;
DAM, D ;
LEE, S ;
COTMAN, CW .
NATURE, 1988, 332 (6162) :360-361
[4]   FIBROBLAST GROWTH-FACTORS [J].
BAIRD, A ;
WALICKE, PA .
BRITISH MEDICAL BULLETIN, 1989, 45 (02) :438-452
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]   SULFATED GLYCOSAMINOGLYCANS MODIFY GROWTH FACTOR-INDUCED NEURITE OUTGROWTH IN PC12 CELLS [J].
DAMON, DH ;
DAMORE, PA ;
WAGNER, JA .
JOURNAL OF CELLULAR PHYSIOLOGY, 1988, 135 (02) :293-300
[7]   ACCELERATED WOUND REPAIR, CELL-PROLIFERATION, AND COLLAGEN ACCUMULATION ARE PRODUCED BY A CARTILAGE-DERIVED GROWTH-FACTOR [J].
DAVIDSON, JM ;
KLAGSBRUN, M ;
HILL, KE ;
BUCKLEY, A ;
SULLIVAN, R ;
BREWER, PS ;
WOODWARD, SC .
JOURNAL OF CELL BIOLOGY, 1985, 100 (04) :1219-1227
[8]   FIBROBLAST GROWTH-FACTOR IS A MITOGEN FOR OLIGODENDROCYTES INVITRO [J].
ECCLESTON, PA ;
SILBERBERG, DH .
DEVELOPMENTAL BRAIN RESEARCH, 1985, 21 (02) :315-318
[9]   BOVINE BRAIN ASTROCYTES EXPRESS BASIC FIBROBLAST GROWTH-FACTOR, A NEUROTROPIC AND ANGIOGENIC MITOGEN [J].
FERRARA, N ;
OUSLEY, F ;
GOSPODAROWICZ, D .
BRAIN RESEARCH, 1988, 462 (02) :223-232
[10]   INVITRO NEURITE EXTENSION BY GRANULE NEURONS IS DEPENDENT UPON ASTROGLIAL-DERIVED FIBROBLAST GROWTH-FACTOR [J].
HATTEN, ME ;
LYNCH, M ;
RYDEL, RE ;
SANCHEZ, J ;
JOSEPHSILVERSTEIN, J ;
MOSCATELLI, D ;
RIFKIN, DB .
DEVELOPMENTAL BIOLOGY, 1988, 125 (02) :280-289