LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 2 of total 2

Search options

  1. Article ; Online: CD99-dependent expansion of myeloid-derived suppressor cells and attenuation of graft-versus-host disease.

    Park, Hyo Jin / Byun, Dahye / Lee, An Hi / Kim, Ju Hyun / Ban, Young Larn / Araki, Masatake / Araki, Kimi / Yamamura, Ken-Ichi / Kim, Inho / Park, Seong Hoe / Jung, Kyeong Cheon

    Molecules and cells

    2012  Volume 33, Issue 3, Page(s) 259–267

    Abstract: ... of graft-versus-host disease by regulating the expansion of myeloid-derived suppressor cells. ... the physiologic function of murine CD99. In a B6 splenocytes → bm12 graft-versus-host disease model, wild-type cells were ... of myeloid-derived suppressor cells. This was confirmed by experiments illustrating that the injection ...

    Abstract CD99 is involved in many cellular events, such as the generation of Hodgkin and Reed-Sternberg cells, T cell costimulation, and leukocyte transendothelial migration. However, these studies have been limited to in vitro or in vivo experiments using CD99-deficient cell lines or anti-CD99 antibodies. In the present study, using CD99-deficient mice established by the exchangeable gene trap method, we investigated the physiologic function of murine CD99. In a B6 splenocytes → bm12 graft-versus-host disease model, wild-type cells were minimally lethal, whereas all mice that received CD99-deficient donor cells developed an early and more severe pathology. Graftversus-host disease in these mice was associated with insufficient expansion of myeloid-derived suppressor cells. This was confirmed by experiments illustrating that the injection of wild-type donor cells depleted of Mac-1(+) cells led to an almost identical disease course as the CD99-deficient donor system. Therefore, these results suggest that CD99 plays a crucial role in the attenuation of graft-versus-host disease by regulating the expansion of myeloid-derived suppressor cells.
    MeSH term(s) 12E7 Antigen ; Animals ; Antigens, CD/genetics ; Antigens, CD/immunology ; Antigens, CD/metabolism ; Cell Movement ; Cell Proliferation ; Cell Transplantation/adverse effects ; Cytokines/blood ; Graft vs Host Disease/metabolism ; Graft vs Host Disease/pathology ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Myeloid Cells/metabolism ; Myeloid Cells/physiology ; Neoplasm Transplantation/pathology ; Spleen/immunology ; Spleen/pathology
    Chemical Substances 12E7 Antigen ; Antigens, CD ; Cd99 protein, mouse ; Cytokines
    Language English
    Publishing date 2012-02-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1148964-9
    ISSN 0219-1032 ; 1016-8478
    ISSN (online) 0219-1032
    ISSN 1016-8478
    DOI 10.1007/s10059-012-2227-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article: CD99-Dependent Expansion of Myeloid-Derived Suppressor Cells and Attenuation of Graft-Versus-Host Disease

    Park, H.J., Seoul National University College of Medicine, Seoul, Republic of Korea / Byun, D.H., Seoul National University College of Medicine, Seoul, Republic of Korea / Lee, A.H., The Catholic University Incheon St. Mary's Hospital, Incheon, Republic of Korea / Kim, J.H., Seoul National University College of Medicine, Seoul, Republic of Korea / Ban, Y.L., Seoul National University College of Medicine, Seoul, Republic of Korea / Araki, Masatake, Kumamoto University, Kumamoto, Japan / Araki, Kimi, Kumamoto University, Kumamoto, Japan / Yamamura, Ken-ichi, Kumamoto University, Kumamoto, Japan / Kim, I.H., Seoul National University College of Medicine, Seoul, Republic of Korea / Park, S.H., Seoul National University College of Medicine, Seoul, Republic of Korea / Jung, K.C., Seoul National University College of Medicine, Seoul, Republic of Korea

    Molecules and Cells

    (Mar 2012)  Volume v. 33, Issue (3), Page(s) p. 259–267

    Abstract: ... of graft-versus-host disease by regulating the expansion of myeloid-derived suppressor cells. ... the physiologic function of murine CD99. In a B6 splenocytes → bm12 graft-versus-host disease model, wild-type cells were ... severe pathology. Graft-versus-host disease in these mice was associated with insufficient expansion ...

    Abstract CD99 is involved in many cellular events, such as the generation of Hodgkin and Reed-Sternberg cells, T cell co-stimulation, and leukocyte transendothelial migration. However, these studies have been limited to in vitro or in vivo experiments using CD99-deficient cell lines or anti-CD99 antibodies. In the present study, using CD99-deficient mice established by the exchangeable gene trap method, we investigated the physiologic function of murine CD99. In a B6 splenocytes → bm12 graft-versus-host disease model, wild-type cells were minimally lethal, whereas all mice that received CD99-deficient donor cells developed an early and more severe pathology. Graft-versus-host disease in these mice was associated with insufficient expansion of myeloid-derived suppressor cells. This was confirmed by experiments illustrating that the injection of wild-type donor cells depleted of Mac-1+ cells led to an almost identical disease course as the CD99-deficient donor system. Therefore, these results suggest that CD99 plays a crucial role in the attenuation of graft-versus-host disease by regulating the expansion of myeloid-derived suppressor cells.
    Keywords CELLS ; CELLULE ; CELULAS
    Language English
    Document type Article
    ISSN 1016-8478
    Database AGRIS - International Information System for the Agricultural Sciences and Technology

    More links

    Kategorien

To top