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Loss of Testicular Orphan Receptor 4 Impairs Normal Myelination in Mouse Forebrain

George Whipple Laboratory for Cancer Research (Y.Z., Y.-T.C., S.X., L.W., Y.-F.L., C.C.), Departments of Pathology (Y.Z., Y.-T.C., S.X., L.W., C.C.), Urology (Y.-F.L., C.C.), Radiation Oncology (C.C.), and The Cancer Center (C.C.), University of Rochester Medical Center, Rochester, New York 14642; and Department of Neurology (S.-S.C.), China Medical University, Taichung 404, Taiwan

Address all correspondence and requests for reprints to: Chawnshang Chang, George Whipple Laboratory for Cancer Research, University of Rochester Medical Center, Rochester, New York 14642. E-mail: chang{at}urmc.rochester.edu.

Testicular orphan nuclear receptor 4 (TR4) has been suggested to play important roles in the development and functioning of the central nervous system (CNS). We find reduced myelination in TR4 knockout (TR4^–/–) mice, which is particularly obvious in forebrains and in early developmental stages. Further analysis reveals that CC-1-positive (CC-1+) oligodendrocytes are decreased in TR4^–/– forebrains. The O4+ signals are also reduced in TR4^–/– forebrains when examined at postnatal d 7. However, the number and proliferation rate of platelet-derived growth factor receptor -positive (PDGFR+) oligodendrocyte precursor cells (OPCs) remain unaffected in these regions, suggesting that loss of TR4 interrupts oligodendrocyte differentiation. This is further supported by the observation that CC-1+ oligodendrocytes derived from 5-bromo-2'-deoxyuridine incorporating OPCs are significantly reduced in TR4^–/– forebrains. We also find higher Jagged1 expression levels in axon fiber-enriched regions in TR4^–/– forebrains, suggesting a more activated Notch signaling in these regions that correlates with previous reports showing that Notch activation inhibits oligodendrocyte differentiation. Together, our results suggest that TR4 is required for proper myelination in the CNS and is particularly important for oligodendrocyte differentiation and maturation in the forebrain regions. The altered Jagged1-Notch signaling in TR4^–/– forebrain underlies a potential mechanism that contributes to the reduced myelination in the forebrain.

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Nuclear Receptors:   TR4