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Activated dendritic cells modulate proliferation and differentiation of human myoblasts.
Ladislau, Leandro; Portilho, Débora M; Courau, Tristan; Solares-Pérez, Alhondra; Negroni, Elisa; Lainé, Jeanne; Klatzmann, David; Bonomo, Adriana; Allenbach, Yves; Benveniste, Olivier; Riederer, Ingo; Savino, Wilson; Mouly, Vincent; Butler-Browne, Gillian; Benjamim, Claudia F.
Afiliação
  • Ladislau L; Institute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Portilho DM; Institut de Myologie, INSERM U974, Sorbonne Université, Paris, France.
  • Courau T; Institut de Myologie, INSERM U974, Sorbonne Université, Paris, France.
  • Solares-Pérez A; Immunology-Immunopathology-Immunotherapy, INSERM U959, Sorbonne Université, Paris, France.
  • Negroni E; Institut de Myologie, INSERM U974, Sorbonne Université, Paris, France.
  • Lainé J; Institut de Myologie, INSERM U974, Sorbonne Université, Paris, France.
  • Klatzmann D; Institut de Myologie, INSERM U974, Sorbonne Université, Paris, France.
  • Bonomo A; Immunology-Immunopathology-Immunotherapy, INSERM U959, Sorbonne Université, Paris, France.
  • Allenbach Y; Laboratory on Thymus Research, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, Brazil.
  • Benveniste O; Institut de Myologie, INSERM U974, Sorbonne Université, Paris, France.
  • Riederer I; Institut de Myologie, INSERM U974, Sorbonne Université, Paris, France.
  • Savino W; Laboratory on Thymus Research, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, Brazil.
  • Mouly V; National Institute of Science and Technology on Neuroimmunomodulation, Rio de Janeiro, Brazil.
  • Butler-Browne G; Laboratory on Thymus Research, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, Brazil.
  • Benjamim CF; National Institute of Science and Technology on Neuroimmunomodulation, Rio de Janeiro, Brazil.
Cell Death Dis ; 9(5): 551, 2018 05 01.
Article em En | MEDLINE | ID: mdl-29748534
Idiopathic Inflammatory Myopathies (IIMs) are a heterogeneous group of autoimmune diseases affecting skeletal muscle tissue homeostasis. They are characterized by muscle weakness and inflammatory infiltration with tissue damage. Amongst the cells in the muscle inflammatory infiltration, dendritic cells (DCs) are potent antigen-presenting and key components in autoimmunity exhibiting an increased activation in inflamed tissues. Since, the IIMs are characterized by the focal necrosis/regeneration and muscle atrophy, we hypothesized that DCs may play a role in these processes. Due to the absence of a reliable in vivo model for IIMs, we first performed co-culture experiments with immature DCs (iDC) or LPS-activated DCs (actDC) and proliferating myoblasts or differentiating myotubes. We demonstrated that both iDC or actDCs tightly interact with myoblasts and myotubes, increased myoblast proliferation and migration, but inhibited myotube differentiation. We also observed that actDCs increased HLA-ABC, HLA-DR, VLA-5, and VLA-6 expression and induced cytokine secretion on myoblasts. In an in vivo regeneration model, the co-injection of human myoblasts and DCs enhanced human myoblast migration, whereas the absolute number of human myofibres was unchanged. In conclusion, we suggest that in the early stages of myositis, DCs may play a crucial role in inducing muscle-damage through cell-cell contact and inflammatory cytokine secretion, leading to muscle regeneration impairment.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Dendríticas / Diferenciação Celular / Mioblastos Esqueléticos / Proliferação de Células Limite: Adult / Female / Humans / Male / Middle aged / Newborn Idioma: En Revista: Cell Death Dis Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Dendríticas / Diferenciação Celular / Mioblastos Esqueléticos / Proliferação de Células Limite: Adult / Female / Humans / Male / Middle aged / Newborn Idioma: En Revista: Cell Death Dis Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido