SSChighCD11bhighLy-6ChighLy-6G low myeloid cells curtail CD4 T cell response by inducible nitric oxide synthase in murine hepatitis

International Journal of Biochemistry and Cell Biology

Volumn 54, Issue , 2014, Pages 89-97

  Zhu, Kai ^a   Zhang, Na ^a   Guo, Nining ^a   Yang, Juhao ^a   Wang, Jianrong ^a   Yang, Chunhui ^a   Yang, Chunfu ^a   Zhu, Lian ^b   Xu, Chunliang ^c   Deng, Qiang ^a   Zhu, Ruihong ^a   Wang, Honglin ^b   Chen, Xuejin ^b   Shi, Yufang ^c   Li, Yao ^b   Leng, Qibin ^a  

^a Chinese Academy of Sciences   (China)

^b SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

^c INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

Author keywords

CD4 T cell response; Concanavalin A; Hepatitis; MDSC; Nitric oxide

Indexed keywords

CONCANAVALIN A; GAMMA INTERFERON; INDUCIBLE NITRIC OXIDE SYNTHASE; INTERLEUKIN 2; NITRIC OXIDE; ACYLTRANSFERASE; CD11B ANTIGEN; FATTY ACID ELONGASES; LY ANTIGEN; LY-6C ANTIGEN, MOUSE; LY6G ANTIGEN, MOUSE; NOS2 PROTEIN, MOUSE; CD4 ANTIGEN;

ADOPTIVE TRANSFER; ANIMAL CELL; ARTICLE; BONE MARROW CELL; CD4+ T LYMPHOCYTE; CD8+ T LYMPHOCYTE; COCULTURE; HEMATOPOIETIC CELL; IN VITRO STUDY; IN VIVO STUDY; LEUKOCYTE; LIVER; LYMPHOCYTE PROLIFERATION; MONOCYTE; MOUSE; MURINE HEPATITIS; NONHUMAN; PHENOTYPE; PRE B LYMPHOCYTE; PROTEIN EXPRESSION; ACUTE LIVER FAILURE; ANIMAL; C57BL MOUSE; CELL PROLIFERATION; FEMALE; FLOW CYTOMETRY; HEPATITIS; IMMUNOLOGICAL TOLERANCE; IMMUNOLOGY; IMMUNOSUPPRESSIVE TREATMENT; LYMPHOCYTE ACTIVATION; MALE; METABOLISM; PATHOLOGY; PHYSIOLOGY; ANIMAL EXPERIMENT; ANIMAL MODEL; CELL PROLIFERATION ASSAY; CONTROLLED STUDY; GIEMSA STAIN; MYELOID DERIVED SUPPRESSOR CELL; SUPPRESSOR CELL;

ACETYLTRANSFERASES; ANIMALS; ANTIGENS, CD11B; ANTIGENS, LY; CD4-POSITIVE T-LYMPHOCYTES; CELL PROLIFERATION; FEMALE; FLOW CYTOMETRY; HEPATITIS; IMMUNE TOLERANCE; IMMUNOSUPPRESSION; LIVER FAILURE, ACUTE; LYMPHOCYTE ACTIVATION; MALE; MICE; MICE, INBRED C57BL; MONOCYTES; MYELOID CELLS; NITRIC OXIDE; NITRIC OXIDE SYNTHASE TYPE II;

MURINAE; MUS;

EID: 84905034165     PISSN: 13572725     EISSN: 18785875     Source Type: Journal    
DOI: 10.1016/j.biocel.2014.07.005     Document Type: Article

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