Pericytes modulate myelination in the central nervous system
Multiple sclerosis is a highly prevalent chronic demyelinating disease of the central nervous system. Remyelination is the major therapeutic goal for this disorder. The lack of detailed knowledge about the cellular and molecular mechanisms involved in myelination restricts the design of effective tr...
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Published in | Journal of cellular physiology Vol. 233; no. 8; pp. 5523 - 5529 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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01.08.2018
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Abstract | Multiple sclerosis is a highly prevalent chronic demyelinating disease of the central nervous system. Remyelination is the major therapeutic goal for this disorder. The lack of detailed knowledge about the cellular and molecular mechanisms involved in myelination restricts the design of effective treatments. A recent study by using [De La Fuente et al. (2017) Cell Reports, 20(8): 1755‐1764] by using state‐of‐the‐art techniques, including pericyte‐deficient mice in combination with induced demyelination, reveal that pericytes participate in central nervous system regeneration. Strikingly, pericytes presence is essential for oligodendrocyte progenitors differentiation and myelin formation during remyelination in the brain. The emerging knowledge from this research will be important for the treatment of multiple sclerosis.
Central nervous system pericytes react to demyelination, and stimulate oligodendrocyte progenitors differentiation. |
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AbstractList | Multiple sclerosis is a highly prevalent chronic demyelinating disease of the central nervous system. Remyelination is the major therapeutic goal for this disorder. The lack of detailed knowledge about the cellular and molecular mechanisms involved in myelination restricts the design of effective treatments. A recent study by using [De La Fuente et al. (2017) Cell Reports, 20(8): 1755‐1764] by using state‐of‐the‐art techniques, including pericyte‐deficient mice in combination with induced demyelination, reveal that pericytes participate in central nervous system regeneration. Strikingly, pericytes presence is essential for oligodendrocyte progenitors differentiation and myelin formation during remyelination in the brain. The emerging knowledge from this research will be important for the treatment of multiple sclerosis.
Central nervous system pericytes react to demyelination, and stimulate oligodendrocyte progenitors differentiation. Multiple sclerosis is a highly prevalent chronic demyelinating disease of the central nervous system. Remyelination is the major therapeutic goal for this disorder. The lack of detailed knowledge about the cellular and molecular mechanisms involved in myelination restricts the design of effective treatments. A recent study by using [De La Fuente et al. (2017) Cell Reports, 20(8): 1755-1764] by using state-of-the-art techniques, including pericyte-deficient mice in combination with induced demyelination, reveal that pericytes participate in central nervous system regeneration. Strikingly, pericytes presence is essential for oligodendrocyte progenitors differentiation and myelin formation during remyelination in the brain. The emerging knowledge from this research will be important for the treatment of multiple sclerosis. Multiple sclerosis is a highly prevalent chronic demyelinating disease of the central nervous system. Remyelination is the major therapeutic goal for this disorder. The lack of detailed knowledge about the cellular and molecular mechanisms involved in myelination restricts the design of effective treatments. De La Fuente et al. (2017) by using state-of-the-art techniques, including pericyte-deficient mice in combination with induced demyelination, reveal that pericytes participate in central nervous system regeneration. Strikingly, pericytes presence is essential for oligodendrocyte progenitors differentiation and myelin formation during remyelination in the brain. The emerging knowledge from this research will be important for the treatment of multiple sclerosis. |
Author | Sena, Isadora F.G. Carvalho‐Tavares, Juliana Mintz, Akiva Cunha, Fernando Q. Alves‐Filho, José C. Andreotti, Julia P. Azevedo, Patrick O. Birbrair, Alexander Cunha, Thiago M. |
AuthorAffiliation | 4 Department of Radiology, Columbia University Medical Center, New York, NY, USA 1 Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil 2 Department of Physiology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil 3 Department of Pharmacology, University of São Paulo, Ribeirão Preto, SP, Brazil |
AuthorAffiliation_xml | – name: 4 Department of Radiology, Columbia University Medical Center, New York, NY, USA – name: 3 Department of Pharmacology, University of São Paulo, Ribeirão Preto, SP, Brazil – name: 1 Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil – name: 2 Department of Physiology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil |
Author_xml | – sequence: 1 givenname: Patrick O. surname: Azevedo fullname: Azevedo, Patrick O. organization: Federal University of Minas Gerais – sequence: 2 givenname: Isadora F.G. surname: Sena fullname: Sena, Isadora F.G. organization: Federal University of Minas Gerais – sequence: 3 givenname: Julia P. surname: Andreotti fullname: Andreotti, Julia P. organization: Federal University of Minas Gerais – sequence: 4 givenname: Juliana surname: Carvalho‐Tavares fullname: Carvalho‐Tavares, Juliana organization: Federal University of Minas Gerais – sequence: 5 givenname: José C. surname: Alves‐Filho fullname: Alves‐Filho, José C. organization: University of São Paulo – sequence: 6 givenname: Thiago M. surname: Cunha fullname: Cunha, Thiago M. organization: University of São Paulo – sequence: 7 givenname: Fernando Q. surname: Cunha fullname: Cunha, Fernando Q. organization: University of São Paulo – sequence: 8 givenname: Akiva surname: Mintz fullname: Mintz, Akiva organization: Columbia University Medical Center – sequence: 9 givenname: Alexander orcidid: 0000-0003-1015-2561 surname: Birbrair fullname: Birbrair, Alexander email: birbrair@icb.ufmg.br organization: Columbia University Medical Center |
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Keywords | myelination multiple sclerosis pericytes central nervous system |
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Snippet | Multiple sclerosis is a highly prevalent chronic demyelinating disease of the central nervous system. Remyelination is the major therapeutic goal for this... |
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SubjectTerms | Autoimmune diseases Brain Central nervous system Demyelination Glial stem cells Molecular modelling Multiple sclerosis Myelin Myelination Nervous system Pericytes Regeneration Rodents |
Title | Pericytes modulate myelination in the central nervous system |
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