z-logo
Premium
Characterization of retinaldehyde dehydrogenase‐2 induction in NG2‐positive glia after spinal cord contusion injury
Author(s) -
Kern Johanna,
Schrage Kirsten,
Koopmans Guido C.,
Joosten Elbert A.,
McCaffery Peter,
Mey Jörg
Publication year - 2007
Publication title -
international journal of developmental neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.761
H-Index - 88
eISSN - 1873-474X
pISSN - 0736-5748
DOI - 10.1016/j.ijdevneu.2006.11.006
Subject(s) - spinal cord , biology , microbiology and biotechnology , regeneration (biology) , tretinoin , retinoic acid , paracrine signalling , receptor , neuroscience , biochemistry , gene
Abstract The transcriptional activator retinoic acid (RA) supports axonal regeneration of several neuronal cell populations in vitro , and it has been suggested that its receptor RARβ2 may be used to support axonal regeneration in the adult mammalian spinal cord. We have previously shown that spinal cord injury induces activity of the RA synthesizing enzyme retinaldehyde dehydrogenase (RALDH)2 in NG2‐positive cells. This report quantifies the increase of RALDH2 protein in the injured spinal cord and characterizes the RALDH2/NG2 expressing cells probably as a unique RA synthesizing subpopulation of activated oligodendrocyte precursors or “polydendrocytes”. In the uninjured spinal cord low levels of RALDH2 are present in oligodendrocytes as well as in the meninges and in blood vessels. Following injury there is a significant increase in RALDH2 in these latter two tissues and, given that the RALDH2/NG2 positive cells are clustered in the same area, this implies that these are specific foci of RA synthesis. It is presumed that these cells release RA in a paracrine fashion in the region of the wound; however, the RALDH2/NG2‐immunoreactive cells expressed the retinoid receptors RARα, RARβ, RXRα and RXRβ, suggesting that RA also serves an autocrine function.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here