TY - JOUR
T1 - Regulation of PD-L1 through direct binding of cholesterol to CRAC motifs
AU - Wang, Qian
AU - Cao, Yunlei
AU - Shen, Lijuan
AU - Xiao, Taoran
AU - Cao, Ruiyu
AU - Wei, Shukun
AU - Tang, Meng
AU - Du, Lingyu
AU - Wu, Hongyi
AU - Wu, Bin
AU - Yu, Yang
AU - Wang, Shuqing
AU - Wen, Maorong
AU - OuYang, Bo
N1 - Publisher Copyright:
© 2022 The Authors.
PY - 2022/8
Y1 - 2022/8
N2 - Cholesterol, an essential molecule for cell structure, function, and viability, plays crucial roles in the development, progression, and survival of cancer cells. Earlier studies have shown that cholesterol-lowering drugs can inhibit the high expression of programmed-death ligand 1 (PD-L1) that contributes to immunoevasion in cancer cells. However, the regulatory mechanism of cell surface PD-L1 abundance by cholesterol is still controversial. Here, using nuclear magnetic resonance and biochemical techniques, we demonstrated that cholesterol can directly bind to the transmembrane domain of PD-L1 through two cholesterol-recognition amino acid consensus (CRAC) motifs, forming a sandwich-like architecture and stabilizing PD-L1 to prevent downstream degradation. Mutations at key binding residues prohibit PD-L1-cholesterol interactions, decreasing the cellular abundance of PD-L1. Our results reveal a unique regulatory mechanism that controls the stability of PD-L1 in cancer cells, providing an alternative method to overcome PD-L1-mediated immunoevasion in cancers.
AB - Cholesterol, an essential molecule for cell structure, function, and viability, plays crucial roles in the development, progression, and survival of cancer cells. Earlier studies have shown that cholesterol-lowering drugs can inhibit the high expression of programmed-death ligand 1 (PD-L1) that contributes to immunoevasion in cancer cells. However, the regulatory mechanism of cell surface PD-L1 abundance by cholesterol is still controversial. Here, using nuclear magnetic resonance and biochemical techniques, we demonstrated that cholesterol can directly bind to the transmembrane domain of PD-L1 through two cholesterol-recognition amino acid consensus (CRAC) motifs, forming a sandwich-like architecture and stabilizing PD-L1 to prevent downstream degradation. Mutations at key binding residues prohibit PD-L1-cholesterol interactions, decreasing the cellular abundance of PD-L1. Our results reveal a unique regulatory mechanism that controls the stability of PD-L1 in cancer cells, providing an alternative method to overcome PD-L1-mediated immunoevasion in cancers.
UR - http://www.scopus.com/inward/record.url?scp=85137125714&partnerID=8YFLogxK
U2 - 10.1126/sciadv.abq4722
DO - 10.1126/sciadv.abq4722
M3 - Article
C2 - 36026448
AN - SCOPUS:85137125714
SN - 2375-2548
VL - 8
JO - Science advances
JF - Science advances
IS - 34
M1 - eabq4722
ER -