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Leptin modulates autophagy in human CD4+CD25- conventional T cells. | LitMetric

Leptin modulates autophagy in human CD4+CD25- conventional T cells.

Metabolism

Dipartimento di Medicina e Chirurgia, Facoltà di Medicina e Chirurgia, Università di Salerno, Baronissi Campus, 84081 Baronissi, Salerno, Italy; IRCCS-MultiMedica, 20138 Milano, Italy. Electronic address:

Published: October 2014

AI Article Synopsis

  • The study explores how the hormone leptin impacts autophagy in human conventional T cells (Tconv) during T cell receptor stimulation.
  • Leptin inhibits autophagy in a dose- and time-dependent manner by activating the mTOR pathway, which can be reversed with mTOR inhibitors like rapamycin.
  • The findings indicate a balance between autophagy and proliferation in Tconv cells during immune activation, highlighting the role of leptin in regulating these processes.

Article Abstract

Objective: In this report we show that the adipocytokine leptin directly modulates autophagy in human CD4(+)CD25(-) conventional (Tconv) T cells.

Results: In vitro treatment with recombinant human leptin determined an inhibition of autophagy during T cell receptor (TCR) stimulation, and this phenomenon was dose- and time-dependent. The events were secondary to the activation of the mammalian-target of rapamycin (mTOR)-pathway induced by leptin, as testified by its reversion induced by mTOR inhibition with rapamycin. At molecular level these phenomena associated with Bcl-2 up-regulation and its interaction with Beclin-1, whose complex exerts a negative effect on autophagy.

Materials/methods: The impact of leptin on autophagy of Tconv cells was determined at biochemical level by western blotting and by flow cytometry; the interaction between BCL-2 and Beclin-1 by co-immunoprecipitation assays.

Conclusions: Our results, suggest that in unconditioned, freshly-isolated human Tconv cells, autophagy and proliferation are controlled by leptin during TCR-engagement, and that both phenomena occur alternatively indicating a balance between these processes during immune activation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180014PMC
http://dx.doi.org/10.1016/j.metabol.2014.06.010DOI Listing

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