How our bodies fight amyloidosis: effects of physiological factors on pathogenic aggregation of amyloidogenic proteins

Arch Biochem Biophys. 2015 Feb 15:568:46-55. doi: 10.1016/j.abb.2015.01.007. Epub 2015 Jan 20.

Abstract

The process of protein aggregation from soluble amyloidogenic proteins to insoluble amyloid fibrils plays significant roles in the onset of over 30 human amyloidogenic diseases, such as Prion disease, Alzheimer's disease and type 2 diabetes mellitus. Amyloid deposits are commonly found in patients suffered from amyloidosis; however, such deposits are rarely seen in healthy individuals, which may be largely attributed to the self-regulation in vivo. A vast number of physiological factors have been demonstrated to directly affect the process of amyloid formation in vivo. In this review, physiological factors that influence amyloidosis, including biological factors (chaperones, natural antibodies, enzymes, lipids and saccharides) and physicochemical factors (metal ions, pH environment, crowding and pressure, etc.), together with the mechanisms underlying these proteostasis effects, are summarized.

Keywords: Amyloidogenic aggregation; Amyloidosis; Biological factors; Physicochemical factors.

Publication types

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

MeSH terms

  • Alzheimer Disease / metabolism
  • Amyloid / analysis
  • Amyloid / metabolism*
  • Amyloidogenic Proteins / analysis
  • Amyloidogenic Proteins / metabolism*
  • Amyloidosis / metabolism*
  • Animals
  • Diabetes Mellitus, Type 2 / metabolism
  • Humans
  • Metals / analysis
  • Metals / metabolism
  • Models, Molecular
  • Molecular Chaperones / analysis
  • Molecular Chaperones / metabolism*
  • Prion Diseases / metabolism
  • Protein Aggregation, Pathological / metabolism*

Substances

  • Amyloid
  • Amyloidogenic Proteins
  • Metals
  • Molecular Chaperones