The insulin-like growth factor binding protein superfamily: new perspectives.

Published

Journal Article

The insulin-like growth factor (IGF) binding proteins (IGFBPs) were initially identified as carrier proteins for IGF-I and IGF-II in a variety of biologic fluids. Their presumed function was to protect IGF peptides from degradation and clearance, increase the half-life of the IGFs, and deliver them to appropriate tissue receptors. The concept of IGFBPs as simple carrier proteins has been complicated, however, by a number of observations: 1) the six IGFBPs vary in their tissue expression and their regulation by other hormones and growth factors; 2) the IGFBPs are subjected to proteolytic degradation, thereby altering their affinities for the IGFs; 3) IGFBP-3 and IGFBP-5, in addition to binding IGFs, also can associate with an acid-labile subunit, thereby increasing further the half-life of the IGFs; 4) in addition to modifying the access of IGF peptides to IGF and insulin receptors, several of the IGFBPs may be capable of increasing IGF action; 5) some of the IGFBPs may be capable of IGF-independent regulation of cell growth; 6) some of the IGFBPs are associated with cell membranes or possibly with membrane receptors; and 7) some of the IGFBPs have nuclear recognition sites and may be found within the nucleus. Additionally, a number of cDNAs identified recently have been found to encode proteins that bind IGFs, but with substantially lower affinities than is the case with IGFBPs. The N-terminal regions of the predicted proteins are structurally homologous to the classic IGFBPs, with conservation of the cysteine-rich region. These observations suggest that these low-affinity binders are members of an IGFBP superfamily, capable of regulating cell growth by both IGF-dependent and IGF-independent mechanisms.insulin-like growth factor, insulin-like growth factor binding proteins.

Full Text

Duke Authors

Cited Authors

  • Rosenfeld, RG; Hwa, V; Wilson, L; Lopez-Bermejo, A; Buckway, C; Burren, C; Choi, WK; Devi, G; Ingermann, A; Graham, D; Minniti, G; Spagnoli, A; Oh, Y

Published Date

  • October 1999

Published In

Volume / Issue

  • 104 / 4 Pt 2

Start / End Page

  • 1018 - 1021

PubMed ID

  • 10506255

Pubmed Central ID

  • 10506255

International Standard Serial Number (ISSN)

  • 0031-4005

Language

  • eng

Conference Location

  • United States