p38 signaling inhibits mTORC1-independent autophagy in senescent human CD8(+) T cells

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Item Type:	Article
Title:	p38 signaling inhibits mTORC1-independent autophagy in senescent human CD8(+) T cells
Creators Name:	Henson, S.M., Lanna, A., Riddell, N.E., Franzese, O., Macaulay, R., Griffiths, S.J., Puleston, D.J., Watson, A.S., Simon, A.K., Tooze, S.A. and Akbar, A.N.
Abstract:	T cell senescence is thought to contribute to immune function decline, but the pathways that mediate senescence in these cells are not clear. Here, we evaluated T cell populations from healthy volunteers and determined that human CD8(+) effector memory T cells that reexpress the naive T cell marker CD45RA have many characteristics of cellular senescence, including decreased proliferation, defective mitochondrial function, and elevated levels of both ROS and p38 MAPK. Despite their apparent senescent state, we determined that these cells secreted high levels of both TNF-α and IFN-γ and showed potent cytotoxic activity. We found that the senescent CD45RA-expressing population engaged anaerobic glycolysis to generate energy for effector functions. Furthermore, inhibition of p38 MAPK signaling in senescent CD8(+) T cells increased their proliferation, telomerase activity, mitochondrial biogenesis, and fitness; however, the extra energy required for these processes did not arise from increased glucose uptake or oxidative phosphorylation. Instead, p38 MAPK blockade in these senescent cells induced an increase in autophagy through enhanced interactions between p38 interacting protein (p38IP) and autophagy protein 9 (ATG9) in an mTOR-independent manner. Together, our findings describe fundamental metabolic requirements of senescent primary human CD8(+) T cells and demonstrate that p38 MAPK blockade reverses senescence via an mTOR-independent pathway.
Keywords:	Autophagy, Autophagy-Related Proteins, CD8-Positive T-Lymphocytes, Cellular Senescence, DNA Damage, Glycolysis, MAP Kinase Signaling System, Mechanistic Target of Rapamycin Complex 1, Membrane Proteins, Mitochondria, Mitochondrial Membrane Potential, Multiprotein Complexes, Oxidative Phosphorylation, TOR Serine-Threonine Kinases, Vesicular Transport Proteins, p38 Mitogen-Activated Protein Kinases
Source:	Journal of Clinical Investigation
ISSN:	1558-8238
Publisher:	American Society for Clinical Investigation
Volume:	124
Number:	9
Page Range:	4004-4016
Date:	2 September 2014
Official Publication:	https://doi.org/10.1172/JCI75051
PubMed:	View item in PubMed

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