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Soluble defense collagens: Sweeping up immune threats.
Casals, Cristina; García-Fojeda, Belén; Minutti, Carlos M.
Afiliación
  • Casals C; Department of Biochemistry and Molecular Biology, Complutense University of Madrid, 28040, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, 28029, Madrid, Spain. Electronic address: ccasalsc@ucm.es.
  • García-Fojeda B; Department of Biochemistry and Molecular Biology, Complutense University of Madrid, 28040, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, 28029, Madrid, Spain.
  • Minutti CM; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, 28029, Madrid, Spain; Immuno-Biology Laboratory, The Francis Crick Institute, NW1 1AT, London, UK.
Mol Immunol ; 112: 291-304, 2019 08.
Article en En | MEDLINE | ID: mdl-31228661
Soluble defense collagens form a group of secreted proteins that are primarily involved in host defense. All defense collagens contain a globular recognition domain contiguous to a collagen-like triple helical domain. They are oligomeric proteins, assembled in multiples of three subunits due to their collagen domains. Members of this group include collectins such as surfactant protein A and D (SP-A, SP-D), and mannan-binding lectin; C1q, the first component of the complement system; adiponectin; and ficolins. All are secreted to tissue cavities or serum. Soluble defense collagens are specialized to respond to infection, triggering the initiation of the complement cascade and/or enhancing phagocytosis of pathogens by macrophages. However, once inflammation is established, C1q, collectins, ficolins, or adiponectin can influence macrophage responses, thereby contributing to resolve the inflammation. In addition, some members of this group of proteins (SP-A, C1q, and adiponectin) modulate tissue-repair functions of macrophages. This review will focus on the molecular mechanisms by which these proteins efficiently defend against immune threats and contribute to tissue repair.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Colágeno / Inmunidad Límite: Animals / Humans Idioma: En Revista: Mol Immunol Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Colágeno / Inmunidad Límite: Animals / Humans Idioma: En Revista: Mol Immunol Año: 2019 Tipo del documento: Article