Literature DB >> 11276120

Protein kinase C and mitogen-activated protein kinase signalling in oligodendrocytes.

R L Stariha1, S U Kim.   

Abstract

Oligodendrocytes (OL) play a significant physiological role in the central nervous system by creating the myelin sheath that allows for the efficient conduction of nerve impulses. Therefore, it is important to understand which signalling cascades define the proliferation, differentiation, survival, and myelin formation potential of these cells. Currently, much of the knowledge in this field has focused on two sets of protein kinase signalling molecules: Protein kinase C (PKC) and the mitogen-activated protein kinases (MAPKs). The roles of these kinases in OL are complex, and appear to be highly dependent on the developmental stage of the OL. Even so, some broad conclusions can be drawn from the multitude of experiments conducted on the roles of PKC and MAPKs in OL. For instance, PKC appears to have a proliferative effect on immature OL, while at the same time having an inhibitory effect on OL differentiation. In mature OL, the effects of PKC include increased process extension and myelin formation. The extracellular signal-regulated (ERK) members of the MAPK family also appear to increase process extensions in mature OL. On the other hand, the c-Jun N-terminal kinase (JNK) and p38 kinase members of the MAPK family appear to regulate apoptotic events in OL. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11276120     DOI: 10.1002/jemt.1052

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  12 in total

1.  Mechanisms of regulation of oligodendrocyte development by p38 mitogen-activated protein kinase.

Authors:  Li-Jin Chew; William Coley; Ying Cheng; Vittorio Gallo
Journal:  J Neurosci       Date:  2010-08-18       Impact factor: 6.167

Review 2.  Oligodendroglial cells and neurotrophins: a polyphonic cantata in major and minor.

Authors:  Hans H Althaus; Sabine Klöppner; Steve Klopfleisch; Matthias Schmitz
Journal:  J Mol Neurosci       Date:  2008-03-08       Impact factor: 3.444

3.  Combination of growth factors enhances remyelination in a cuprizone-induced demyelination mouse model.

Authors:  Shalini Kumar; Juan Carlos Biancotti; Masahiro Yamaguchi; Jean de Vellis
Journal:  Neurochem Res       Date:  2006-12-21       Impact factor: 3.996

4.  Dystroglycan modulates the ability of insulin-like growth factor-1 to promote oligodendrocyte differentiation.

Authors:  Jason Galvin; Christopher Eyermann; Holly Colognato
Journal:  J Neurosci Res       Date:  2010-11-15       Impact factor: 4.164

5.  Tyrosine phosphatases Shp1 and Shp2 have unique and opposing roles in oligodendrocyte development.

Authors:  Emory Kuo; Daniel K Park; Iva D Tzvetanova; Cindy V Leiton; Brian S Cho; Holly Colognato
Journal:  J Neurochem       Date:  2010-02-02       Impact factor: 5.372

6.  Tumor-induced STAT3 signaling in myeloid cells impairs dendritic cell generation by decreasing PKCβII abundance.

Authors:  Matthew R Farren; Louise M Carlson; Colleen S Netherby; Inna Lindner; Pui-Kai Li; Dmitry I Gabrilovich; Scott I Abrams; Kelvin P Lee
Journal:  Sci Signal       Date:  2014-02-18       Impact factor: 8.192

7.  Astrocytes protect oligodendrocyte precursor cells via MEK/ERK and PI3K/Akt signaling.

Authors:  Ken Arai; Eng H Lo
Journal:  J Neurosci Res       Date:  2010-03       Impact factor: 4.164

8.  Very large G protein-coupled receptor 1 regulates myelin-associated glycoprotein via Gαs/Gαq-mediated protein kinases A/C.

Authors:  Daesung Shin; Shu-Ting Lin; Ying-Hui Fu; Louis J Ptácek
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-04       Impact factor: 11.205

Review 9.  Myelin management by the 18.5-kDa and 21.5-kDa classic myelin basic protein isoforms.

Authors:  George Harauz; Joan M Boggs
Journal:  J Neurochem       Date:  2013-03-06       Impact factor: 5.372

10.  Nucleus-localized 21.5-kDa myelin basic protein promotes oligodendrocyte proliferation and enhances neurite outgrowth in coculture, unlike the plasma membrane-associated 18.5-kDa isoform.

Authors:  Graham S T Smith; Bożena Samborska; Steven P Hawley; Jordan M Klaiman; Todd E Gillis; Nina Jones; Joan M Boggs; George Harauz
Journal:  J Neurosci Res       Date:  2012-11-27       Impact factor: 4.164

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