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Concomitant type I IFN and M-CSF signaling reprograms monocyte differentiation and drives pro-tumoral arginase production.

EBioMedicine. 2019-01;

TongYuanyuan, ZhouLuyang, YangLimin, GuoPanpan, CaoYanlan, QinF Xiao-Feng, LiuJiang

Products/Services Used	Details	Operation
Catalog Antibody	… Technology (Erk1/2, #4695; pErk1/2, #4370; CSF1R, #3152; Stat3, #9139; pStat3-Y705, #9145; arginase-1, #93668; pStat1-Y701, #7649; Stat1, #14994), Santa Cruz (GAPDH, #sc-32,233), BD (ARG1, 610,708, for immunofluorescent staining), Genscript (Actin, #A00730) and …	Get A Quote

摘要

Type I IFN-based therapies against solid malignancies have yielded only limited success. How IFN affects tumor-associated macrophage (TAM) compartment to impact the therapeutic outcomes are not well understood.

关键词

Anti-tumor immunity，Arginase，M-CSF，Monocyte maturation，Tumor-associated macrophages，Type I

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Concomitant type I IFN and M-CSF signaling reprograms monocyte differentiation and drives pro-tumoral arginase production.

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