Inhibition of phosphodiesterase‐4 promotes oligodendrocyte precursor cell differentiation and enhances CNS remyelination. Issue 12 (21st October 2013)

• Record Type: Journal Article
• Authors: Syed, Yasir A.; Baer, Alexandra; Hofer, Matthias P.; González, Ginez A.; Rundle, Jon; Myrta, Szymon; Huang, Jeffrey K.; Zhao, Chao; Rossner, Moritz J.; Trotter, Matthew W. B.; Lubec, Gert; Franklin, Robin J. M.; Kotter, Mark R.
• Is Part Of: EMBO molecular medicine. Volume 5:Issue 12(2013:Dec.)
• Page Start: 1918
• Page End: 1934
• Publication Date: 2013-10-21
• Subjects: Molecular biology -- Periodicals; Medical genetics -- Periodicals; Pathology, Molecular -- Periodicals; 616.04205
• DOI: 10.1002/emmm.201303123
• Languages: English
• ISSNs: 1757-4676

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="emmm201303123-sec-0001" sec-type="section"> <p>The increasing effectiveness of new disease‐modifying drugs that suppress disease activity in multiple sclerosis has opened up opportunities for regenerative medicines that enhance remyelination and potentially slow disease progression. Although several new targets for therapeutic enhancement of remyelination have emerged, few lend themselves readily to conventional drug development. Here, we used transcription profiling to identify mitogen‐activated protein kinase (Mapk) signalling as an important regulator involved in the differentiation of oligodendrocyte progenitor cells (OPCs) into oligodendrocytes. We show in tissue culture that activation of Mapk signalling by elevation of intracellular levels of cyclic adenosine monophosphate (cAMP) using administration of either dibutyryl‐cAMP or inhibitors of the cAMP‐hydrolysing enzyme phosphodiesterase‐4 (Pde4) enhances OPC differentiation. Finally, we demonstrate that systemic delivery of a Pde4 inhibitor leads to enhanced differentiation of OPCs within focal areas of toxin‐induced demyelination and a consequent acceleration of remyelination. These data reveal a novel approach to therapeutic enhancement of remyelination amenable to pharmacological intervention and hence with significant potential for translation.</p> </sec> </abstract>