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Complement cascade functions during brain development and neurodegeneration.
Fatoba, Oluwaseun; Itokazu, Takahide; Yamashita, Toshihide.
Afiliação
  • Fatoba O; Department of Molecular Neuroscience, Graduate School of Medicine, Osaka University, Suita, Japan.
  • Itokazu T; WPI-Immunology Frontier Research Center, Osaka University, Suita, Japan.
  • Yamashita T; Department of Molecular Neuroscience, Graduate School of Medicine, Osaka University, Suita, Japan.
FEBS J ; 289(8): 2085-2109, 2022 04.
Article em En | MEDLINE | ID: mdl-33599083
The complement system, an essential tightly regulated innate immune system, is a key regulator of normal central nervous system (CNS) development and function. However, aberrant complement component expression and activation in the brain may culminate into marked neuroinflammatory response, neurodegenerative processes and cognitive impairment. Over the years, complement-mediated neuroinflammatory responses and complement-driven neurodegeneration have been increasingly implicated in the pathogenesis of a wide spectrum of CNS disorders. This review describes how complement system contributes to normal brain development and function. We also discuss how pathologic insults such as misfolded proteins, lipid droplet/lipid droplet-associated protein or glycosaminoglycan accumulation could trigger complement-mediated neuroinflammatory responses and neurodegenerative process in neurodegenerative proteinopathies, age-related macular degeneration and neurodegenerative lysosomal storage disorders.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas Limite: Humans Idioma: En Revista: FEBS J Assunto da revista: BIOQUIMICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Japão País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas Limite: Humans Idioma: En Revista: FEBS J Assunto da revista: BIOQUIMICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Japão País de publicação: Reino Unido