Inhibitory insulin-like growth factor-binding protein: cloning, complete sequence, and physiological regulation

D LaTour, S Mohan, TA Linkhart… - Molecular …, 1990 - academic.oup.com
D LaTour, S Mohan, TA Linkhart, DJ Baylinkt, DD Strong
Molecular Endocrinology, 1990academic.oup.com
In this study we report the preparation of a human osteosarcoma cell cDNA library and
describe the isolation and sequence determination of a clone encoding the complete
sequence of a novel human insulin-like growth factor (IGF)-binding protein (hlGFBP-4).
Previous work indicated that hlGFBP-4 is the predominant IGFBP expressed by human
osteoblast-like cells, and that IGFBP-4 binds and inhibits the mitogenic activities of IGF-I and
IGF-II. Sequence determination revealed that hlGFBP-4 is a unique gene product with …
Abstract
In this study we report the preparation of a human osteosarcoma cell cDNA library and describe the isolation and sequence determination of a clone encoding the complete sequence of a novel human insulin-like growth factor (IGF)-binding protein (hlGFBP-4). Previous work indicated that hlGFBP-4 is the predominant IGFBP expressed by human osteoblast- like cells, and that IGFBP-4 binds and inhibits the mitogenic activities of IGF-I and IGF-II. Sequence determination revealed that hlGFBP-4 is a unique gene product with significant amino- and carboxy-terminal sequence similarity to three other known IGFBPs. Identical alignment of 18 cysteines in IGFBP-4 and the three other IGFBPs is a key structural feature of this protein family. In vitro studies of human osteoblast-like cells suggest that PTH regulates the expression of hlGFBP-4 and that the PTH effect is mediated through a cAMP mechanism. hlGFBP-4 mRNA was also expressed in skin fibroblasts, and thus, this inhibitory IGFBP could be an important physiological regulator of IGF actions in bone cells and other cell types as well.
Oxford University Press