Abnormalities of IGF-I signaling in the pathogenesis of diseases of the bone, brain, and fetoplacental unit in humans

Am J Physiol Endocrinol Metab. 2008 Nov;295(5):E991-9. doi: 10.1152/ajpendo.90452.2008. Epub 2008 Aug 19.

Abstract

IGF-I action is essential for the regulation of tissue formation and remodeling, bone growth, prenatal growth, brain development, and muscle metabolism. Cellular effects of IGF-I are mediated through the IGF-I receptor, a transmembrane tyrosine kinase that phosphorylates intracellular substrates, resulting in the activation of multiple intracellular signaling cascades. Dysregulation of IGF-I actions due to impairment in the postreceptor signaling machinery may contribute to multiple diseases in humans. This article will review current information on IGF-I signaling and illustrate recent results demonstrating how impaired IGF-I signaling and action may contribute to the pathogenesis of human diseases, including osteoporosis, neurodegenerative disorders, and reduced fetal growth in utero.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bone Diseases / etiology
  • Bone Diseases / metabolism
  • Bone Diseases / physiopathology*
  • Brain Diseases / etiology
  • Brain Diseases / metabolism
  • Brain Diseases / physiopathology*
  • Female
  • Fetal Diseases / etiology
  • Fetal Diseases / metabolism
  • Fetal Diseases / physiopathology
  • Humans
  • Insulin-Like Growth Factor I / physiology*
  • Placenta / metabolism
  • Placenta / pathology
  • Placenta / physiopathology
  • Placenta Diseases / etiology
  • Placenta Diseases / metabolism
  • Placenta Diseases / physiopathology
  • Pregnancy
  • Signal Transduction / physiology*

Substances

  • Insulin-Like Growth Factor I