El papel de la fak en la acantólisis del pénfigo vulgar en un modelo murino

• Autores: María Pilar Gil Sánchez
• Directores de la Tesis: Agustín España Alonso (dir. tes.), María Jesús López Zabalza (dir. tes.)
• Lectura: En la Universidad de Navarra ( España ) en 2012
• Idioma: español
• Número de páginas: 189
• Tribunal Calificador de la Tesis: Ignacio Querol Nasarre (presid.), Pedro Redondo Bellón (secret.), Ricardo Suárez Fernández (voc.), José Manuel Mascaró Galy (voc.), Carlos Gabriel de Miguel Vázquez (voc.)
• Materias:
  • Química
    • Bioquímica
  • Ciencias médicas
    • Ciencias clínicas
      • Dermatología
• Enlaces
  • Tesis en acceso abierto en: Dadun
• Resumen

  • Pemphigus vulgaris (PV) is an autoimmune blistering skin disease characterized by suprabasal acantholysis, and autoantibodies against desmoglein 3 localized on desmosomes. In addition, caspases also seem to participate in this blistering disease. Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase involved in cytoskeleton remodelling and formation and disassembly of cell adhesion structures. We have previously demonstrated that HER (human epidermal growth factor receptor related) isoforms, Src (Rous sarcoma) and mTOR (mammalian target of rapamycin), three molecules implicated in signalling processes, take part in suprabasal acantholysis and apoptosis induced by PV-IgG in a mouse model. Our aim was to investigate if upregulation of FAK is implicated in the development of PV lesions. Herein, using a mouse model, PV-IgG administration showed an increased level of FAK phosphorylated on 397 and 925 tyrosine residues in the basal layer of epidermis. When mice were pretreated with a FAK inhibitor the acantholysis of the basal layer of epidermis was absent. More interestingly, we observed that phosphorylated FAK (Y397/925) decreased when HER isoforms, Src, mTOR, and pan-caspases inhibitors were employed before PV-IgG administration. In addition, pretreatment with the FAK inhibitor before PV-IgG injection avoided the changes of both Bax and Bcl-2 expression and caspases-9 and –3 activities induced by PV-IgG. Finally, FAK inhibitor reduced expression of phosphorylated Src and mTOR in the basal cells of epidermis. In conclusion, our data reveal a novel biochemical mechanism for phosphorylated FAK (Y397/925) in PV development involving HER isoforms, Src and mTOR kinases.