The Shc protein Rai enhances T-cell survival under hypoxia.
Mattia CriscuoliCristina UlivieriIrene FilippiSara MonaciGiuditta GuerriniBianca CrifòDomiziana De TommasoGiuliana PelicciCosima T BaldariCormac T TaylorFabio CarraroAntonella NaldiniPublished in: Journal of cellular physiology (2020)
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.
Keyphrases
- endothelial cells
- cell death
- induced apoptosis
- nuclear factor
- cell cycle arrest
- poor prognosis
- binding protein
- toll like receptor
- cell proliferation
- type diabetes
- amino acid
- endoplasmic reticulum stress
- stem cells
- mesenchymal stem cells
- skeletal muscle
- metabolic syndrome
- immune response
- high fat diet induced
- mass spectrometry
- insulin resistance
- small molecule
- bone marrow
- cell therapy
- anti inflammatory
- single molecule