Inflammation in ALS and SMA: sorting out the good from the evil

Neurobiol Dis. 2010 Mar;37(3):493-502. doi: 10.1016/j.nbd.2009.10.005. Epub 2009 Oct 13.

Abstract

Indices of neuroinflammation are found in a variety of diseases of the CNS including amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA). Over the years, neuroinflammation, in degenerative disorders of the CNS, has evolved from being regarded as an innocent bystander accomplishing its housekeeping function secondary to neurodegeneration to being considered as a bona fide contributor to the disease process and, in some situations, as a putative initiator of the disease. Herein, we will review neuroinflammation in both ALS and SMA not only from the angle of neuropathology but also from the angle of its potential role in the pathogenesis and treatment of these two dreadful paralytic disorders.

Publication types

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

MeSH terms

  • Amyotrophic Lateral Sclerosis / genetics
  • Amyotrophic Lateral Sclerosis / immunology*
  • Amyotrophic Lateral Sclerosis / physiopathology
  • Astrocytes / immunology
  • Cytoprotection / physiology
  • Gliosis / genetics
  • Gliosis / immunology*
  • Gliosis / physiopathology
  • Humans
  • Microglia / immunology
  • Muscular Atrophy, Spinal / genetics
  • Muscular Atrophy, Spinal / immunology*
  • Muscular Atrophy, Spinal / physiopathology
  • Myelitis / genetics
  • Myelitis / immunology*
  • Myelitis / physiopathology
  • Nerve Degeneration / immunology
  • Nerve Degeneration / physiopathology
  • Neuroglia / immunology*
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Superoxide Dismutase-1

Substances

  • SOD1 protein, human
  • Superoxide Dismutase
  • Superoxide Dismutase-1