肿瘤微环境
癌症研究
音猬因子
巨噬细胞极化
细胞生物学
生物
肿瘤进展
T细胞
CXCL10型
巨噬细胞
CD8型
免疫学
免疫系统
趋化因子
信号转导
癌症
肿瘤细胞
体外
生物化学
遗传学
作者
Amy J. Petty,Ang Li,Xinyi Wang,Rui Dai,Benjamin Heyman,David S. Hsu,Xin Huang,Yiping Yang
摘要
Tumor-associated macrophages (TAMs) usually display an antiinflammatory M2-like phenotype to facilitate tumor growth. However, what drives M2 polarization of TAMs and how TAMs suppress antitumor immunity within the tumor microenvironment (TME) remain largely undefined. Using several murine tumor models, we showed that hedgehog (Hh) signaling in myeloid cells is critical for TAM M2 polarization and tumor growth. We also found that tumor cells secrete sonic hedgehog (SHH), an Hh ligand, and that tumor-derived SHH drives TAM M2 polarization. Furthermore, Hh-induced functional polarization in TAMs suppresses CD8+ T cell recruitment to the TME through the inhibition of CXCL9 and CXCL10 production by TAMs. Last, we demonstrated that Krüppel-like factor 4 (Klf4) mediates Hh-dependent TAM M2 polarization and the immunosuppressive function. Collectively, these findings highlight a critical role for tumor-derived SHH in promoting TAM M2 polarization, a mechanism for TAM-mediated immunosuppression, and may provide insights into the design of new cancer immunotherapeutic strategies.
科研通智能强力驱动
Strongly Powered by AbleSci AI