LRP2, an auxiliary receptor that controls sonic hedgehog signaling in development and disease

Dev Dyn. 2016 May;245(5):569-79. doi: 10.1002/dvdy.24394. Epub 2016 Mar 4.

Abstract

To fulfill their multiple roles in organ development and adult tissue homeostasis, hedgehog (HH) morphogens act through their receptor Patched (PTCH) on target cells. However, HH actions also require HH binding proteins, auxiliary cell surface receptors that agonize or antagonize morphogen signaling in a context-dependent manner. Here, we discuss recent findings on the LDL receptor-related protein 2 (LRP2), an exemplary HH binding protein that modulates sonic hedgehog activities in stem and progenitor cell niches in embryonic and adult tissues. LRP2 functions are crucial for developmental processes in a number of tissues, including the brain, the eye, and the heart, and defects in this receptor pathway are the cause of devastating congenital diseases in humans. Developmental Dynamics 245:569-579, 2016. © 2016 Wiley Periodicals, Inc.

Keywords: Donnai-Barrow syndrome; LDL receptor related proteins; LRP2; endocytosis; forebrain development; hedgehog binding proteins; holoprosencephaly; morphogen signaling; sonic hedgehog.

Publication types

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

MeSH terms

  • Animals
  • Congenital Abnormalities / embryology
  • Congenital Abnormalities / etiology
  • Embryonic Development
  • Hedgehog Proteins / metabolism*
  • Humans
  • Low Density Lipoprotein Receptor-Related Protein-2 / deficiency
  • Low Density Lipoprotein Receptor-Related Protein-2 / physiology*
  • Morphogenesis
  • Signal Transduction / physiology

Substances

  • Hedgehog Proteins
  • Low Density Lipoprotein Receptor-Related Protein-2