• No results found

Phenotypic and functional dissection of myeloid-derived suppressor cells

N/A
N/A
Protected

Academic year: 2020

Share "Phenotypic and functional dissection of myeloid-derived suppressor cells"

Copied!
5
0
0

Loading.... (view fulltext now)

Full text

Figure

Fig. 1 Strategies of G-, M-, andoxidase,Treginterleukin 10,MDSCinducivle nitric oxide synthase,NOF-MDSCs for T cellsuppression
Fig. 2 Tumor-mediated MDSC formation.suppressor cell,oxide synthase, G-CSF granulocyte col-ony-stimulating factor, GM-CSF granulocyte macrophage colony-stimulating factor, M-CSF macrophage colony-stimulating factor, IL-6 interleukin 6, HSC hematopoietic stem cell, MDSC myeloid-derived ROS reactive oxygen species, iNOS inducible nitric IL-10 interleukin 10, Treg regulatory T cell

References

Related documents

MDSCs: polymorphonucler myeloid-derived suppressor cells; Prkar1a: protein kinase cAMP-dependent type I regulatory subunit alpha; PSA: prostate specific antigen;

In this study, we analyzed and characterized the functions of MDSCs under the influence of mouse mesangial cells (MMCs) in a hyperglycemic environment and investigated

Myeloid derived suppressor cells (MDSCs); arginase-1; inducible nitric oxide synthase (iNOS); reactive oxygen species (ROS); chronic inflammation; dendritic cells (DCs);

Figure 3: Arginase and iNOS levels in MDSCs isolated from spleen and tumor microenvironment following RA190 treatment or RPN13 knock down in vitro.. The levels of Arginase and

firm the overlapping features of our EV-MDSCs with myeloid cells from cancer patients, we compared the transcriptomic profile of EV-MDSCs with those of monocytes sorted from the

ASCT: Autologous stem cell transplantation; BM: Bone marrow; E- MDSCs: Early-stage MDSCs; G-MDSCs: Granulocytic MDSCs; ISS: International staging system; MDSCs:

conspire to promote breast cancer metastasis. MDSC activity in cancer promotion. Different subsets of MDSCs are recruited to the tumor microenvironment and promote tumor

Rab7 GTPase siRNA knocking down in isolated bone marrow lal –/– MDSCs or HD1B cells not only reduced over-activation of mTOR and its downstream effector S6, but also decreased