The blockage of Notch signalling promoted the generation of polymorphonuclear myeloid-derived suppressor cells with lower immunosuppression

• Published in: European journal of cancer (1990) 2016-11, Vol.68, p.90-105
• Main Authors: Wang, Shu-Hong, Lu, Qing-Yang, Guo, Ya-Huan, Song, Yuan-Yuan, Liu, Pei-Jun, Wang, Yao-Chun
• Format: Article
• Language: English
• Subjects: Animals; Antigen Presentation; Bone Marrow; Dendritic Cells; Development; Hematology, Oncology and Palliative Medicine; Immune Tolerance; Immunoglobulin J Recombination Signal Sequence-Binding Protein - genetics; Immunoglobulin J Recombination Signal Sequence-Binding Protein - immunology; Immunosuppression; In Vitro Techniques; Intercellular Signaling Peptides and Proteins - immunology; Intracellular Signaling Peptides and Proteins - immunology; Jagged-1 Protein - immunology; Jagged-2 Protein - immunology; Lymph Nodes - cytology; MDSCs; Membrane Proteins - immunology; Mice; Myeloid-Derived Suppressor Cells - immunology; Neoplasms - immunology; Notch signalling; Peritoneal Cavity - cytology; Receptors, Notch - immunology; RNA, Small Interfering; Signal Transduction - immunology; Spleen - cytology; Stat3 pathway; STAT3 Transcription Factor - immunology; T-Lymphocytes
• ISSN: 0959-8049; 1879-0852
• DOI: 10.1016/j.ejca.2016.08.019

Abstract Myeloid-derived suppressor cells (MDSCs) mostly consisting of polymorphonuclear (PMN)-MDSCs and mononuclear MDSCs have been considered to play critical roles in immunosuppression, angiogenesis, invasion and metastases of various tumours. However, it is still unclear the regulated mechanisms underlying the generation and immunosuppression of two major MDSC subsets. Here, we report Notch signalling was inhibited significantly in tumour-bearing mouse MDSCs, in which PMN-MDSCs were the major population. MDSCs without recombination signal binding protein-Jк (RBP-J), the critical transcription factor mediating signalling from all four mammalian Notch receptors, reduced their ability of inhibiting the proliferation and activation of allogenic T cells. RBP-J-deficient MDSCs could not down-regulate the expression of co-stimulation molecules on dendritic cells (DCs). The antigen presentation capacity of DCs co-cultured with RBP-J-deficient MDSCs was not impaired in contrast to controls. Moreover, we show the blockage of Notch signalling could improve the generation of PMN-MDSCs but inhibit the production of mononuclear MDSCs both in vitro and in vivo . Stat3 pathway was suppressed in MDSCs blocked Notch signalling and Stat3 activation by IL-6 could reverse the phenotype and immunosuppression of Notch signalling–deficient MDSCs. Therefore, targeting Notch signalling may be an effective therapeutic strategy in tumour therapy.