TRP channels in disease

Subcell Biochem. 2007:45:253-71. doi: 10.1007/978-1-4020-6191-2_9.

Abstract

The transient receptor potential (TRP) channels are a large family of proteins with six main subfamilies termed the TRPC (canonical), TRPV (vanilloid), TRPM (melastatin), TRPP (polycystin), TRPML (mucolipin), and TRPA (ankyrin) groups. The sheer number of different TRPs with distinct functions supports the statement that these channels are involved in a wide range of processes ranging from sensing of thermal and chemical signals to reloading intracellular stores after responding to an extracellular stimulus. Mutations in TRPs are linked to pathophysiology and specific diseases. An understanding of the role of TRPs in normal physiology is just beginning; the progression from mutations in TRPs to pathophysiology and disease will follow. In this review, we focus on two distinct aspects of TRP channel physiology, the role of TRP channels in intracellular Ca2+ homeostasis, and their role in the transduction of painful stimuli in sensory neurons.

Publication types

  • Review

MeSH terms

  • Asthma / physiopathology
  • Calcium / physiology*
  • Calcium Channels / physiology
  • Calcium Signaling / physiology
  • Diabetes Mellitus, Type 1 / physiopathology
  • Homeostasis / physiology
  • Humans
  • Nerve Tissue Proteins / physiology
  • Pain / physiopathology*
  • Polycystic Kidney Diseases / physiopathology*
  • TRPA1 Cation Channel
  • TRPM Cation Channels / physiology
  • TRPP Cation Channels / metabolism
  • TRPV Cation Channels / physiology
  • Transient Receptor Potential Channels / genetics
  • Transient Receptor Potential Channels / physiology*

Substances

  • Calcium Channels
  • Nerve Tissue Proteins
  • TRPA1 Cation Channel
  • TRPA1 protein, human
  • TRPM Cation Channels
  • TRPM8 protein, human
  • TRPP Cation Channels
  • TRPV Cation Channels
  • TRPV1 protein, human
  • Transient Receptor Potential Channels
  • polycystic kidney disease 1 protein
  • polycystic kidney disease 2 protein
  • Calcium