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Differential expression and localization of IGF-I and IGF binding proteins in inflamed rat colon
被引:22
作者:
Zeeh, JM
Mohapatra, N
Lund, PK
Eysselein, VE
McRoberts, JA
[1
]
机构:
[1] Univ Calif Los Angeles, Los Angeles Cty Harbor Med Ctr, Div Gastroenterol, Torrance, CA 90509 USA
[2] Univ Essen Gesamthsch, Dept Gastroenterol, Essen, Germany
[3] Univ N Carolina, Dept Physiol, Chapel Hill, NC USA
来源:
JOURNAL OF RECEPTOR AND SIGNAL TRANSDUCTION RESEARCH
|
1998年
/
18卷
/
4-6期
关键词:
D O I:
10.3109/10799899809047747
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Recent studies indicate increased insulin-like growth factor I (IGF-I) expression and altered expression of IGF binding proteins (IGFBP) in the bowel during experimental colitis. This study analyzes the cellular sites of altered IGF-I and IGFBP-expression in large bowel of rats with experimental colitis. Colitis was induced by colonic instillation of 2, 4, 6-trinitrobenzenesulfonic (TNB) acid in ethanol. Animals were sacrificed at 7 days after induction of colitis. Cryostat sections of colon from TNB-treated and control rats were hybridized with S-35-labeled antisense probes for IGF-I, IGFBP-3, IGFBP-4 and IGFBP-5. IGF-I mRNA was up-regulated in lamina propria cells, submucosa and smooth muscle of inflamed colon. IGFBP3 mRNA was localized to lamina propria and was down-regulated in inflamed colon. IGFBP-4 and IGFBP-5 mRNAs were both upregulated in inflamed colon. IGFBP-4 mRNA was increased in lamina propria, submucosa and smooth muscle, whereas IGFBP-5 mRNA was increased in smooth muscle. Increased IGF-I expression in mesenchymal layers of colon during experimental colitis supports the hypothesis that IGF-X contributes to hyperplasia and fibrosis in response to inflammation. Altered expression of IGFBP-3, IGFBP-4 and IGFBP-5 in specific bowel layers during colitis suggests that they play a role in modulating IGF-I action.
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页码:265 / 280
页数:16
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