| Literature DB >> 32099075 |
Yanjun Jia1, Qiuyun Yang1, Yanping Wang1, Wenyan Li1, Xuemei Chen1, Tao Xu1, Zhirui Tian1, Minxuan Feng1, Liang Zhang1, Wenjing Tang1, Na Tian2, Lina Zhou1, Wenxia Song3, Xiaodong Zhao4.
Abstract
Activated phosphoinositide 3-kinase δ syndrome (APDS) is an autosomal-dominant combined immunodeficiency disorder resulting from pathogenic gain-of-function (GOF) mutations in the PIK3CD gene. Patients with APDS display abnormal T cell homeostasis. However, the mechanisms by which PIK3CD GOF contributes to this feature remain unknown. Here, with a cohort of children with PIK3CD GOF mutations from multiple regions of China and a corresponding CRISPR/Cas9 gene-edited mouse model, we reported that hyperactive PI3Kδ disrupted TNaive cell homeostasis in the periphery by intrinsically promoting the growth, proliferation, and activation of TNaive cells. Our results showed that PIK3CD GOF resulted in loss of the quiescence-associated gene expression profile in naive T cells and promoted naive T cells to overgrow, hyperproliferate and acquire an activated functional status. Naive PIK3CD GOF T cells exhibited an enhanced glycolytic capacity and reduced mitochondrial respiration in the resting or activated state. Blocking glycolysis abrogated the abnormal splenic T cell pool and reversed the overactivated phenotype induced by PIK3CD GOF in vivo and in vitro. These results suggest that enhanced aerobic glycolysis is required for PIK3CD GOF-induced overactivation of naive T cells and provide a potential therapeutic approach for targeting glycolysis to treat patients with APDS as well as other immune disorders.Entities:
Keywords: Activated phosphoinositide3-kinase δ syndrome; Aerobic glycolysis; Naive T cells; PIK3CD; Primary immunodeficiency disorders
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Year: 2020 PMID: 32099075 PMCID: PMC8245563 DOI: 10.1038/s41423-020-0379-x
Source DB: PubMed Journal: Cell Mol Immunol ISSN: 1672-7681 Impact factor: 22.096