Entorhinal deafferentation induces upregulation of SPARC in the mouse hippocampus

Brain Res Mol Brain Res. 2005 Nov 18;141(1):58-65. doi: 10.1016/j.molbrainres.2005.08.003. Epub 2005 Aug 31.

Abstract

SPARC is a matricellular protein that modulates cell-cell and cell-matrix interactions by virtue of its antiproliferative and counteradhesive properties. Here, we report the denervation-induced upregulation of SPARC mRNA and protein in the mouse hippocampus following transections of the entorhinal afferents. Northern blot analysis showed that SPARC mRNA was upregulated in a transient manner in the deafferented mouse hippocampus. In situ hybridization and immunohistochemistry confirmed the temporal upregulation of both SPARC mRNA and protein specifically in the denervated areas, which initiated at 7 days postlesion, reached the maximum at 15 as well as 30 days postlesion, and subsided towards normal levels by 60 days postlesion. Double labeling by either a combination of in situ hybridization for SPARC mRNA with immunohistochemistry for glial fibrillary acidic protein or double immunofluorescence staining for both proteins in the hippocampus revealed that SPARC-expressing cells are reactive astrocytes. In respect to the spatiotemporal alterations of SPARC expression in the denervated hippocampus, we suggest that SPARC may be involved in modulation of the denervation-induced plasticity processes such as glial cell proliferation, axonal sprouting and subsequent synaptogenesis in the hippocampus following entorhinal deafferentation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Afferent Pathways / metabolism
  • Afferent Pathways / pathology
  • Animals
  • Astrocytes / cytology
  • Astrocytes / metabolism
  • Denervation*
  • Entorhinal Cortex* / cytology
  • Entorhinal Cortex* / physiology
  • Female
  • Hippocampus / cytology
  • Hippocampus / metabolism*
  • Hippocampus / pathology
  • In Situ Hybridization
  • Mice
  • Osteonectin / genetics
  • Osteonectin / metabolism*
  • RNA, Messenger / metabolism
  • Up-Regulation*

Substances

  • Osteonectin
  • RNA, Messenger