ER-phagy and mitophagy programs in human CD4+ memory T cells before and after activation

Abstract

T lymphocytes can remain in a resting state for very long times. Encountering their cognate antigen triggers their activation, leading to an increase in cell size, proliferation, enhanced protein production, and secretion of signaling molecules. This activation and clonal expansion phase is followed by a contraction phase, with a reduction in cell size, eventually leading to cell death or progression to resting (memory) cells. Here, we show that human resting primary CD4+ memory T cells degrade endoplasmic reticulum (ER) and mitochondrial portions via ER-phagy and mitophagy, respectively. The temporary interruption of ER and mitochondria turnover coupled with a transient induction of the unfolded protein response results in the enlargement of the ER and cellular volume. Cell growth is stabilized and then reversed during the clonal expansion and contraction phases by the resumption of a catabolic phase characterized by the reactivation of ER-phagy and outer mitochondrial membrane (OMM)-phagy. Collectively, our data show that the maintenance and the activity of human CD4+ memory T cells rely on finely tuned execution of anabolic and catabolic programs that regulate mass and activity of the ER and mitochondria.