The motorized RhoGAP myosin IXb (Myo9b) in leukocytes regulates experimental autoimmune encephalomyelitis induction and recovery

Liu Z., Xu Y., Zhang X., Song J., Sorokin L., Bähler M.

Research article (journal) | Peer reviewed

Abstract

Myo9b regulates leukocyte migration by controlling RhoA signaling. Here we assessed its role in active experimental autoimmune encephalomyelitis (EAE). Myo9b-/- mice show a delay in the onset of EAE symptoms. The delay in disease onset was accompanied by reduced numbers of Th1 and Th17 cells in the CNS. Myo9b-/- mice showed no recovery from disease symptoms and exhibited elevated numbers of both Th17 cells and CD11b+ macrophages. Bone marrow chimeric mice demonstrated that the absence of a leukocyte source of Myo9b was responsible for the delayed leukocyte infiltration into the CNS, delayed EAE onset and lack of recovery.

Details about the publication

JournalJournal of Neuroimmunology (J Neuroimmunol)
Volume282
Issuenull
Page range25-32
StatusPublished
Release year2015
Language in which the publication is writtenEnglish
DOI10.1016/j.jneuroim.2015.03.014
Link to the full texthttp://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84928569951&origin=inward
KeywordsBone marrow chimeric mice; Clinical features; Experimental autoimmune encephalomyelitis; Myosin IXb; RhoGAP

Authors from the University of Münster

Bähler, Martin
Professorship of Molecular Cell Biology (Prof. Bähler)
Sorokin, Lydia
Institute of Physiological Chemistry and Pathobiochemistry