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Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi ; 21(1): 76-8, 2005 Jan.
Article in Chinese | MEDLINE | ID: mdl-15629090

ABSTRACT

AIM: To induce and expand dendritic cells (DC) from rat bone marrow in vitro and identify their biological characterization. METHODS: The rat bone marrow cells were collected and cultured for 48 hours and the floating cells were removed. Then IL-4 and GM-CSF were added into the fresh medium. After 2 weeks, the morphological character of the cultured DCs was observed under light microscope and transmission electron microscope. Expressions of MHC class II molecule, B7-1 and B7-2 were detected by flow cytometry. The cultured DCs were co-cultured with allogenic T cells derived from rat spleen. T cell proliferation was measured by MTT colorimetry. RESULTS: The cultured DCs had the typical morphological characterization of DC, and the expression rates of MHC class II molecule, B7-1 and B7-2 were 74.2%, 81% and 76% respectively. The cultured DCs could notably stimulate the proliferation of allogeneic T cells. CONCLUSION: The adherent culture of rat bone marrow cells, and co-culture with IL-4 and GM-CSF can obtain a number of high purity of DCs, which lay the foundation for study on DC's function.


Subject(s)
Bone Marrow/immunology , Dendritic Cells/cytology , Dendritic Cells/immunology , Animals , Cell Proliferation , Coculture Techniques , Dendritic Cells/ultrastructure , Female , Gene Expression Regulation , Histocompatibility Antigens Class II/metabolism , Microscopy, Electron, Transmission , Rats , T-Lymphocytes/immunology
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