Extracellular acidosis restricts one-carbon metabolism and preserves T cell stemness.
Hongcheng ChengYajing QiuYue XuLi ChenKaili MaMengyuan TaoLuke FrankiwHongli YinErmei XieXiaoli PanJing DuZhe WangWenjie ZhuMei ChenLianjun ZhangGuideng LiPublished in: Nature metabolism (2023)
The accumulation of acidic metabolic waste products within the tumor microenvironment inhibits effector functions of tumor-infiltrating lymphocytes (TILs). However, it remains unclear how an acidic environment affects T cell metabolism and differentiation. Here we show that prolonged exposure to acid reprograms T cell intracellular metabolism and mitochondrial fitness and preserves T cell stemness. Mechanistically, elevated extracellular acidosis impairs methionine uptake and metabolism via downregulation of SLC7A5, therefore altering H3K27me3 deposition at the promoters of key T cell stemness genes. These changes promote the maintenance of a 'stem-like memory' state and improve long-term in vivo persistence and anti-tumor efficacy in mice. Our findings not only reveal an unexpected capacity of extracellular acidosis to maintain the stem-like properties of T cells, but also advance our understanding of how methionine metabolism affects T cell stemness.
Keyphrases
- stem cells
- epithelial mesenchymal transition
- genome wide
- physical activity
- oxidative stress
- dendritic cells
- cell proliferation
- ionic liquid
- type diabetes
- metabolic syndrome
- heavy metals
- body composition
- regulatory t cells
- dna methylation
- skeletal muscle
- immune response
- reactive oxygen species
- working memory
- high fat diet induced
- insulin resistance
- sewage sludge