Vps10 family proteins and the retromer complex in aging-related neurodegeneration and diabetes. Review uri icon

Overview

abstract

  • Members of the vacuolar protein sorting 10 (Vps10) family of receptors (including sortilin, SorL1, SorCS1, SorCS2, and SorCS3) play pleiotropic functions in protein trafficking and intracellular and intercellular signaling in neuronal and non-neuronal cells. Interactions have been documented between Vps10 family members and the retromer coat complex, a key component of the intracellular trafficking apparatus that sorts cargo from the early endosome to the trans-Golgi network. In recent years, genes encoding several members of the Vps10 family of proteins, as well as components of the retromer coat complex, have been implicated as genetic risk factors for sporadic and autosomal dominant forms of neurodegenerative diseases, including Alzheimer's disease, frontotemporal lobar degeneration, and Parkinson's disease, with risk for type 2 diabetes mellitus and atherosclerosis. In addition to their functions in protein trafficking, the Vps10 family proteins modulate neurotrophic signaling pathways. Sortilin can impact the intracellular response to brain-derived neurotrophic factor (BDNF) by regulating anterograde trafficking of Trk receptors to the synapse and direct control of BDNF levels, while both sortilin and SorCS2 function as cell surface receptors to mediate acute responses to proneurotrophins. This mini-review and symposium will highlight the emerging data from this rapidly growing area of research implicating the Vps10 family of receptors and the retromer in physiological intracellular trafficking signaling by neurotrophins and in the pathogenesis of neurodegeneration.

publication date

  • October 10, 2012

Research

keywords

  • Aging
  • Diabetes Mellitus, Type 2
  • Nerve Growth Factors
  • Neurodegenerative Diseases
  • Receptors, Cell Surface

Identity

PubMed Central ID

  • PMC3576841

Scopus Document Identifier

  • 84867270258

Digital Object Identifier (DOI)

  • 10.1523/JNEUROSCI.3359-12.2012

PubMed ID

  • 23055476

Additional Document Info

volume

  • 32

issue

  • 41