Hedgehog signaling promotes tumor-associated macrophage polarization to suppress intratumoral CD8+ T cell recruitment

被引:232
作者
Petty, Amy J. [1 ,2 ]
Li, Ang [2 ]
Wang, Xinyi [1 ,2 ]
Dai, Rui [1 ,2 ]
Heyman, Benjamin [2 ]
Hsu, David [2 ]
Huang, Xiaopei [2 ]
Yang, Yiping [2 ,3 ]
机构
[1] Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC USA
[2] Duke Univ, Dept Med, Div Hematol Malignancies & Cellular Therapy, Durham, NC USA
[3] Duke Univ, Dept Immunol, Durham, NC USA
关键词
MYELOID CELLS; EXPRESSION; GENE; TRANSCRIPTION; REQUIREMENT; MECHANISMS; PLASTICITY; CHEMOKINES; DIVERSITY; BLOCKADE;
D O I
10.1172/JCI128644
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
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 Kruppel-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.
引用
收藏
页码:5151 / 5162
页数:12
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