Intersectin scaffold proteins and their role in cell signaling and endocytosis

Biochim Biophys Acta Mol Cell Res. 2017 Jan;1864(1):23-30. doi: 10.1016/j.bbamcr.2016.10.005. Epub 2016 Oct 12.

Abstract

Intersectins (ITSNs) are a family of multi-domain proteins involved in regulation of diverse cellular pathways. These scaffold proteins are well known for regulating endocytosis but also play important roles in cell signaling pathways including kinase regulation and Ras activation. ITSNs participate in several human cancers, such as neuroblastomas and glioblastomas, while their downregulation is associated with lung injury. Alterations in ITSN expression have been found in neurodegenerative diseases such as Down Syndrome and Alzheimer's disease. Binding proteins for ITSNs include endocytic regulatory factors, cytoskeleton related proteins (i.e. actin or dynamin), signaling proteins as well as herpes virus proteins. This review will summarize recent studies on ITSNs, highlighting the importance of these scaffold proteins in the aforementioned processes.

Keywords: Actin; Cancer; Endocytosis; Intersectin; Neurons; Scaffold.

Publication types

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

MeSH terms

  • Adaptor Proteins, Vesicular Transport / genetics*
  • Adaptor Proteins, Vesicular Transport / metabolism
  • Alzheimer Disease / genetics
  • Alzheimer Disease / metabolism
  • Alzheimer Disease / pathology
  • Animals
  • Brain Neoplasms / genetics
  • Brain Neoplasms / metabolism
  • Brain Neoplasms / pathology
  • Cytoskeletal Proteins / genetics*
  • Cytoskeletal Proteins / metabolism
  • Down Syndrome / genetics
  • Down Syndrome / metabolism
  • Down Syndrome / pathology
  • Endocytosis / genetics*
  • Gene Expression Regulation*
  • Glioblastoma / genetics
  • Glioblastoma / metabolism
  • Glioblastoma / pathology
  • Humans
  • Lung Injury / genetics
  • Lung Injury / metabolism
  • Lung Injury / pathology
  • Neuroblastoma / genetics
  • Neuroblastoma / metabolism
  • Neuroblastoma / pathology
  • Oncogene Protein p21(ras) / genetics
  • Oncogene Protein p21(ras) / metabolism
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protein Kinases / genetics
  • Protein Kinases / metabolism
  • Signal Transduction*

Substances

  • Adaptor Proteins, Vesicular Transport
  • Cytoskeletal Proteins
  • Protein Isoforms
  • intersectin 1
  • Protein Kinases
  • Oncogene Protein p21(ras)