Premium
PPAR δ agonists stimulate oligodendrocyte differentiation in tissue culture
Author(s) -
Saluja Inderjeet,
Granneman James G.,
Skoff Robert P.
Publication year - 2001
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/1098-1136(200103)33:3<191::aid-glia1018>3.0.co;2-m
Subject(s) - agonist , biology , medicine , oligodendrocyte , peroxisome proliferator activated receptor , endocrinology , receptor , ppar agonist , microbiology and biotechnology , myelin , biochemistry , central nervous system
Peroxisome proliferator–activated receptors (PPARs) are ligand‐activated transcription factors of the nuclear hormone receptor superfamily that have been described as master genes that switch cells from an undifferentiated phenotype to a differentiated phenotype. In the present investigation, we examined the possibility that ligands for PPARs are potent activators of oligodendrocyte (OL) differentiation and/or proliferation. Primary glial cultures and enriched OL cultures of neonatal mouse cerebra were treated with three different PPAR agonists: a PPAR γ–selective agonist, a PPAR δ–selective agonist, and a pan agonist selective for both PPAR γ and δ. Treatment with PPAR γ agonist does not have an effect on the differentiation of OLs; however, PPAR δ agonist and the pan agonist treatment accelerates the differentiation of OLs within 24 h of application in mixed glial cultures. The number of OLs with processes and huge membrane sheets increases two‐ to threefold in both groups. The increase in the size of the sheets is also mirrored by changes in the intensity and distribution of myelin basic protein (MBP) and proteolipid protein (PLP) mRNAs. As compared to controls, the PPAR δ agonist–treated groups contain more OLs that have MBP and PLP mRNA extending into distal processes. These results indicate that PPAR δ plays a significant role in the maturation of OLs and regulates the size of OL sheets. BrdU immunostaining reveals that these agonists do not significantly stimulate proliferation of OLs expressing glycolipids. The studies in enriched OL cultures reproduce the effects of the PPAR agonists seen in the mixed glial cultures, indicating that the effect of the PPAR agonists is directly on the OLs and not via astrocytes. In the enriched cultures, the total number of OLs increases significantly in the PPAR δ agonist–treated groups, but BrdU immunostaining does not show an increased proliferation of cells. These findings suggest that PPAR δ increases the survival of cells and/or prevents cell death in enriched cultures. Although PPAR δ is expressed in various cell types, its role as a factor in the transcriptional regulation of OL differentiation has not been explored. We show for the first time that a ligand that serves as an agonist for PPAR δ activates the program of OL differentiation in primary and enriched OL cultures. GLIA 33:191–204, 2001. © 2001 Wiley‐Liss, Inc.