Emerging roles for intersectin (ITSN) in regulating signaling and disease pathways

Int J Mol Sci. 2013 Apr 10;14(4):7829-52. doi: 10.3390/ijms14047829.

Abstract

Intersectins (ITSNs) represent a family of multi-domain adaptor proteins that regulate endocytosis and cell signaling. ITSN genes are highly conserved and present in all metazoan genomes examined thus far. Lower eukaryotes have only one ITSN gene, whereas higher eukaryotes have two ITSN genes. ITSN was first identified as an endocytic scaffold protein, and numerous studies reveal a conserved role for ITSN in endocytosis. Subsequently, ITSNs were found to regulate multiple signaling pathways including receptor tyrosine kinases (RTKs), GTPases, and phosphatidylinositol 3-kinase Class 2beta (PI3KC2β). ITSN has also been implicated in diseases such as Down Syndrome (DS), Alzheimer Disease (AD), and other neurodegenerative disorders. This review summarizes the evolutionary conservation of ITSN, the latest research on the role of ITSN in endocytosis, the emerging roles of ITSN in regulating cell signaling pathways, and the involvement of ITSN in human diseases such as DS, AD, and cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adaptor Proteins, Vesicular Transport / genetics
  • Adaptor Proteins, Vesicular Transport / metabolism*
  • Alzheimer Disease / genetics
  • Alzheimer Disease / metabolism*
  • Alzheimer Disease / pathology
  • Animals
  • Class II Phosphatidylinositol 3-Kinases / genetics
  • Class II Phosphatidylinositol 3-Kinases / metabolism
  • Down Syndrome / genetics
  • Down Syndrome / metabolism*
  • Down Syndrome / pathology
  • Endocytosis / genetics
  • GTP Phosphohydrolases / genetics
  • GTP Phosphohydrolases / metabolism
  • Humans
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Signal Transduction*

Substances

  • Adaptor Proteins, Vesicular Transport
  • intersectin 1
  • Class II Phosphatidylinositol 3-Kinases
  • PIK3C2B protein, human
  • Receptor Protein-Tyrosine Kinases
  • GTP Phosphohydrolases