Semaphorin 6A improves functional recovery in conjunction with motor training after cerebral ischemia

PLoS One. 2010 May 20;5(5):e10737. doi: 10.1371/journal.pone.0010737.

Abstract

We have previously identified Semaphorin 6a (Sema6A) as an upregulated gene product in a gene expression screen in cortical ischemia [1]. Semaphorin 6a was regulated during the recovery phase following ischemia in the cortex. Semaphorin 6a is a member of the superfamily of semaphorins involved in axon guidance and other functions. We hypothesized that the upregulation indicates a crucial role of this molecule in post-stroke rewiring of the brain. Here we have tested this hypothesis by overexpressing semaphorin 6a in the cortex by microinjection of a modified AAV2-virus. A circumscribed cortical infarct was induced, and the recovery of rats monitored for up to 4 weeks using a well-established test battery (accelerated rotarod training paradigm, cylinder test, adhesive tape removal). We observed a significant improvement in post-ischemic recovery of animals injected with the semaphorin 6a virus versus animals treated with a control virus. We conclude that semaphorin 6a overexpressed in the cortex enhances recovery after cerebral ischemia. Semaphorin 6a may represent a novel therapeutic candidate for the treatment of chronic stroke.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Ischemia / metabolism
  • Brain Ischemia / physiopathology*
  • Cell Line
  • Dependovirus / genetics
  • Humans
  • Motor Activity / physiology*
  • Physical Conditioning, Animal*
  • Psychomotor Performance
  • Rats
  • Recovery of Function / physiology*
  • Semaphorins / metabolism*
  • Stroke / metabolism
  • Stroke / physiopathology

Substances

  • Sema6A protein, rat
  • Semaphorins