Characterization of thromboxane A2 receptor signaling in developing rat oligodendrocytes: Nuclear receptor localization and stimulation of myelin basic protein …

S Ramamurthy, F Mir, RM Gould… - Journal of …, 2006 - Wiley Online Library
S Ramamurthy, F Mir, RM Gould, GCL Breton
Journal of neuroscience research, 2006Wiley Online Library
The present work investigates the role of thromboxane A2 (TXA2) receptors in the
development of oligodendrocytes (OLGs). The results demonstrate that the proteins of the
TXA2 signaling pathway, ie, cyclooxygenase (COX‐1), TXA2 synthase (TS), and TXA2
receptor (TPR) are expressed in the developing rat brain during myelination. Furthermore,
culture of OLG progenitor cells (OPCs) revealed that the expression levels of these proteins
as well as TXA2 synthesis increase during OLG maturation. Separate studies established …
Abstract
The present work investigates the role of thromboxane A2 (TXA2) receptors in the development of oligodendrocytes (OLGs). The results demonstrate that the proteins of the TXA2 signaling pathway, i.e., cyclooxygenase (COX‐1), TXA2 synthase (TS), and TXA2 receptor (TPR) are expressed in the developing rat brain during myelination. Furthermore, culture of OLG progenitor cells (OPCs) revealed that the expression levels of these proteins as well as TXA2 synthesis increase during OLG maturation. Separate studies established that activation of TPRs by the agonist U46619 increases intracellular calcium in both OPCs and OLGs as visualized by digital fluorescence imaging. Immunocytochemical staining demonstrated that TPRs are localized in the plasma membrane and perinuclear compartments in OPCs. However, during OLG differentiation, TPRs shift their localization pattern and also become associated with the nuclear compartment. This shift to nuclear localization was confirmed by biochemical analysis in cultured cells and by immunocytochemical analysis in developing rat brain. Finally, it was found that U46619 activation of TPRs in maturing OLGs resulted in enhanced myelin basic protein (MBP) expression. Alternatively, inhibition of endogenous TPR signaling led to reduced MBP expression. Furthermore, TPR‐mediated MBP expression was found to be associated with increased transcription from the MBP promoter using a MBP‐luciferase reporter. Collectively, these findings suggest a novel TPR signaling pathway in OLGs and a potential role for this signaling during OLG maturation and myelin production. © 2006 Wiley‐Liss, Inc.
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