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T-cell calcium dynamics visualized in a ratiometric tdTomato-GCaMP6f transgenic reporter mouse.
Dong, Tobias X; Othy, Shivashankar; Jairaman, Amit; Skupsky, Jonathan; Zavala, Angel; Parker, Ian; Dynes, Joseph L; Cahalan, Michael D.
Afiliação
  • Dong TX; Department of Physiology and Biophysics, University of California, Irvine, United States.
  • Othy S; Department of Physiology and Biophysics, University of California, Irvine, United States.
  • Jairaman A; Department of Physiology and Biophysics, University of California, Irvine, United States.
  • Skupsky J; Department of Physiology and Biophysics, University of California, Irvine, United States.
  • Zavala A; Department of Medicine, University of California, Irvine, United States.
  • Parker I; Department of Physiology and Biophysics, University of California, Irvine, United States.
  • Dynes JL; Department of Physiology and Biophysics, University of California, Irvine, United States.
  • Cahalan MD; Department of Neurobiology & Behavior, University of California, Irvine, United States.
Elife ; 62017 12 14.
Article em En | MEDLINE | ID: mdl-29239725
Calcium is an essential cellular messenger that regulates numerous functions in living organisms. Here, we describe development and characterization of 'Salsa6f', a fusion of GCaMP6f and tdTomato optimized for cell tracking while monitoring cytosolic Ca2+, and a transgenic Ca2+ reporter mouse with Salsa6f targeted to the Rosa26 locus for Cre-dependent expression in specific cell types. The development and function of T cells was unaffected in Cd4-Salsa6f mice. We describe Ca2+ signals reported by Salsa6f during T cell receptor activation in naive T cells, helper Th17 T cells and regulatory T cells, and Ca2+ signals mediated in T cells by an activator of mechanosensitive Piezo1 channels. Transgenic expression of Salsa6f enables ratiometric imaging of Ca2+ signals in complex tissue environments found in vivo. Two-photon imaging of migrating T cells in the steady-state lymph node revealed both cell-wide and localized sub-cellular Ca2+ transients ('sparkles') as cells migrate.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T / Canais de Cálcio / Cálcio / Sinalização do Cálcio / Imagem Óptica Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T / Canais de Cálcio / Cálcio / Sinalização do Cálcio / Imagem Óptica Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article