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The Shc protein Rai enhances T-cell survival under hypoxia
Authors:Mattia Criscuoli  Cristina Ulivieri  Irene Filippi  Sara Monaci  Giuditta Guerrini  Bianca Crifò  Domiziana De Tommaso  Giuliana Pelicci  Cosima T Baldari  Cormac T Taylor  Fabio Carraro  Antonella Naldini
Institution:1. Cellular and Molecular Physiology Unit, Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy;2. Department of Life Sciences, University of Siena, Siena, Italy;3. Cellular and Molecular Physiology Unit, Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy

Istituto Toscano Tumori, Firenze, Italy;4. Department of Systems Biology, UCD Conway Institute and School of Medicine, University College Dublin, Dublin, Ireland;5. Department of Experimental Oncology, European Institute of Oncology IRCCS, Milan, Italy

Department of Translational Medicine, Piemonte Orientale University “Amedeo Avogadro”, Novara, Italy;6. Istituto Toscano Tumori, Firenze, Italy

Department of Medical Biotechnologies, University of Siena, Siena, Italy

Abstract:Hypoxia occurs in physiological and pathological conditions. T cells experience hypoxia in pathological and physiological conditions as well as in lymphoid organs. Indeed, hypoxia-inducible factor 1α (HIF-1α) affects T cell survival and functions. Rai, an Shc family protein member, exerts pro-survival effects in hypoxic neuroblastoma cells. Since Rai is also expressed in T cells, we here investigated its role in hypoxic T cells. In this work, hypoxia differently affected cell survival, proapoptotic, and metabolic programs in T cells, depending upon Rai expression. By using Jurkat cells stably expressing Rai and splenocytes from Rai?/?mice, we demonstrated that Rai promotes T cell survival and affects cell metabolism under hypoxia. Upon exposure to hypoxia, Jurkat T cells expressing Rai show (a) higher HIF-1α protein levels; (b) a decreased cell death and increased Akt/extracellular-signal-regulated kinase phosphorylation; (c) a decreased expression of proapoptotic markers, including caspase activities and poly(ADP-ribose) polymerase cleavage; (d) an increased glucose and lactate metabolism; (e) an increased activation of nuclear factor-kB pathway. The opposite effects were observed in hypoxic splenocytes from Rai?/?mice. Thus, Rai plays an important role in hypoxic signaling and may be relevant in the protection of T cells against hypoxia.
Keywords:cell survival  HIF-1α  hypoxia  Shc protein  T cell
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