TY - JOUR
T1 - Scramblase TMEM16F terminates T cell receptor signaling to restrict T cell exhaustion
AU - Hu, Yu
AU - Kim, Ji Hyung
AU - He, Kangmin
AU - Wan, Qi
AU - Kim, Jessica
AU - Flach, Melanie
AU - Kirchhausen, Tom
AU - Vortkamp, Andrea
AU - Winau, Florian
PY - 2016/11/14
Y1 - 2016/11/14
N2 - In chronic infection, T cells become hyporesponsive to antigenic stimulation to prevent immunopathology. Here, we show that TMEM16F is required to curb excessive T cell responses in chronic infection with virus. TMEM16F-deficient T cells are hyperactivated during the early phase of infection, exhibiting increased proliferation and cytokine production. Interestingly, this overactivation ultimately leads to severe T cell exhaustion and the inability of the host to control viral burden. Mechanistically, we identify TMEM16F as the dominant lipid scramblase in T lymphocytes that transports phospholipids across membranes. TMEM16F is located in late endosomes, where it facilitates the generation of multivesicular bodies for TCR degradation and signal termination. Consequently, TMEM16F deficiency results in sustained signaling and augmented T cell activation. Our results demonstrate that scramblase restricts TCR responses to avoid overactivation, ensuring a well-balanced immune response in chronic infectious disease.
AB - In chronic infection, T cells become hyporesponsive to antigenic stimulation to prevent immunopathology. Here, we show that TMEM16F is required to curb excessive T cell responses in chronic infection with virus. TMEM16F-deficient T cells are hyperactivated during the early phase of infection, exhibiting increased proliferation and cytokine production. Interestingly, this overactivation ultimately leads to severe T cell exhaustion and the inability of the host to control viral burden. Mechanistically, we identify TMEM16F as the dominant lipid scramblase in T lymphocytes that transports phospholipids across membranes. TMEM16F is located in late endosomes, where it facilitates the generation of multivesicular bodies for TCR degradation and signal termination. Consequently, TMEM16F deficiency results in sustained signaling and augmented T cell activation. Our results demonstrate that scramblase restricts TCR responses to avoid overactivation, ensuring a well-balanced immune response in chronic infectious disease.
UR - http://www.scopus.com/inward/record.url?scp=84999749837&partnerID=8YFLogxK
U2 - 10.1084/jem.20160612
DO - 10.1084/jem.20160612
M3 - Article
C2 - 27810927
AN - SCOPUS:84999749837
SN - 0022-1007
VL - 213
SP - 2759
EP - 2772
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 12
ER -