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Divalent cations regulate the organization of integrins alpha v beta 3 and alpha v beta 5 on the cell surface.
Stuiver, I; Ruggeri, Z; Smith, J W.
Afiliación
  • Stuiver I; Department of Molecular and Experimental Medicine and Vascular Biology, Scripps Research Institute, La Jolla, California, USA.
J Cell Physiol ; 168(3): 521-31, 1996 Sep.
Article en En | MEDLINE | ID: mdl-8816906
Extracellular divalent cations are important regulators of integrin ligand binding activity. In this study we evaluated how divalent cations affect the organization of integrins into focal adhesion sites. Integrins alpha v beta 3 and alpha v beta 5 were compared because they share a high degree of structural homology and because both integrins mediate cell adhesion to vitronectin. On MG-63 osteosarcoma cells, we found that both the extent and pattern of integrin organization was regulated by the type of extracellular divalent ion. Integrin alpha v beta 3 organized in focal contacts when Mn2+ or Mg2+ was present, but not in Ca2+. In contrast, alpha v beta 5 organized in focal contacts only when Ca2+ or Mg2+ was present. Integrin alpha v beta 5 clustered in a centrally located punctate field on the ventral surface of the cell in the presence of Mn2+. These observations reveal a previously unappreciated role for divalent ions in regulating the organization of integrins into focal adhesion sites.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glicoproteínas de Membrana Plaquetaria / Antígenos CD / Moléculas de Adhesión Celular / Integrinas / Receptores de Vitronectina / Cadenas beta de Integrinas Límite: Humans Idioma: En Revista: J Cell Physiol Año: 1996 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glicoproteínas de Membrana Plaquetaria / Antígenos CD / Moléculas de Adhesión Celular / Integrinas / Receptores de Vitronectina / Cadenas beta de Integrinas Límite: Humans Idioma: En Revista: J Cell Physiol Año: 1996 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos