IGF BINDING PROTEIN-2 GENE-EXPRESSION AND THE LOCATION OF IGF-I AND IGF-II IN FETAL-RAT LUNG

被引:0
|
作者
KLEMPT, M [1 ]
HUTCHINS, AM [1 ]
GLUCKMAN, PD [1 ]
SKINNER, SJM [1 ]
机构
[1] UNIV AUCKLAND,SCH MED,DEPT PAEDIAT,MOLEC ENDOCRINOL LABS,AUCKLAND,NEW ZEALAND
来源
DEVELOPMENT | 1992年 / 115卷 / 03期
关键词
IGF; BINDING PROTEIN; LUNG; FETUS; GROWTH;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Binding proteins for the insulin-like growth factors (IGFBPs) are important modulators of the biological actions of IGF-I and IGF-II. The generation of IGFBPs within developing organs, and their spatial arrangement, may similarly determine IGF action at specific microanatomical sites. In situ hybridization studies with late gestation (days 16,18 and 20) fetal rat lung using a cDNA probe for IGFBP-2 showed strong gene expression in the fetal lung epithelial structures (alveoli and airways). The sites of IGFBP-2 gene expression were associated with immunoreactive IGF-II at the apical surface of the epithelium. By day 20, there was also some IGFBP-2 gene expression and immunoreactive IGF-II at discrete sites in the mesenchyme. In contrast, immunoreactive IGF-I was found predominantly distributed in a punctate pattern, consistent with its presence in the lumen or walls of small vessels or capillaries, and in a granular, intracellular form in both epithelial and mesenchymal cells. These studies suggest that endogenously generated IGFBP-2 may determine the distribution of IGF-II, principally at the apical surface of lung epithelia. IGF-I does not co-localise with IGF-II peptide or the sites of IGFBP-2 gene expression. We conclude that the spatial distributions of these two related growth factors are separately controlled, to some extent by endogenously generated binding proteins.
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页码:765 / 772
页数:8
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