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1.
China Journal of Chinese Materia Medica ; (24): 407-410, 2006.
Article in Chinese | WPRIM | ID: wpr-350927

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of Zhikepingon the oxyradical andintercellular adhesion molecule-1 (ICAM-1) of experimental early atherosclerosis.</p><p><b>METHOD</b>The model of SD rat early atherosclerosis was induced by cholesterol diet. The suspension of Zhikeping and simvastatin were administered intragastrically, respectively. After 10 weeks, the serum lipids, superoxide dismutase (SOD) and maleic dialdehyde (MDA) were detected by automatic biochemistry analyzer. ICAM-1 and its expression of mRNA in aortic wall were detected- by immunohistochemistry and RT-PCR, respectively. Aortic histomorphology was cbserved by HE stainning.</p><p><b>RESULT</b>The results showed that the serum lipids, superoxide dismutase (SOD) and maleic dialdehyde (MDA) of treated groups were obviously improved as compared with those of the control group. The tissue pathological damage was improved indifferent degree, and ICAM-1 and its expression of mRNA was decreased obviously.</p><p><b>CONCLUSION</b>It is suggested the mechanism of anti-atherosclerosis of Zhikeping have close relationship with the function of its anti-oxidizing and anti-adhesiveness that can protect aortic endothelial cell.</p>


Subject(s)
Animals , Male , Rats , Aorta , Metabolism , Atherosclerosis , Metabolism , Pathology , Curcuma , Chemistry , Curcumin , Pharmacology , Intercellular Adhesion Molecule-1 , Genetics , Lipids , Blood , Malondialdehyde , Blood , Plants, Medicinal , Chemistry , RNA, Messenger , Genetics , Rats, Sprague-Dawley , Superoxide Dismutase , Blood
2.
Chinese Journal of Hematology ; (12): 632-635, 2003.
Article in Chinese | WPRIM | ID: wpr-354813

ABSTRACT

<p><b>OBJECTIVE</b>To explore the specific cytotoxic T lymphocyte (CTL) induced by dendritic cells (DC), which were transfected by the plasmid pC53-SN3 encoding p53 gene.</p><p><b>METHODS</b>DC derived from HLA-A2(+) mononuclear cells of the 24-lung cancer patients was transfected with the plasmid pC53-SN3 by lipofectamine and then co-cultured with auto-unpurified T cells to induce potent CTL (T-pC53-SN3). The cytolysis of specific CTL against Calu-6, a HLA-A2(+) human lung cancer cell line, was measured by using lactate dehydrogenase (LDH) releasing assay.</p><p><b>RESULTS</b>The expression of CD(1a) and CD(83), the correlative markers of DC, increased apparently after transfected with plasmid pC53-SN3, the expression rate was (5.45 +/- 0.89)% and (3.26 +/- 0.47)% versus (52.15 +/- 11.56)% and (25.78 +/- 12.35)%. CD(14) decreased apparently, but other DC correlative markers of CD(1a), CD(40), CD(86), and HLA-DR remained almost the same as that before transfection. Compared with T-IL-2, the CTL derived from PBMNC stimulated by IL-2 (100 U/ml), the cytolytic activity of T-pC53-SN3 against Calu-6 cell line showed a significant increase, but cytolytic activity was 56.79 +/- 15.67 and 39.33 +/- 9.88, respectively, when effect cells: target cells was 10:1. The expression of the CD(8), CD(69), and CD(45)RO/CD(8) of T-pC53-SN3 cells increased significantly, but that of CD(3), CD(4), CD(86), ect, was not significantly different from those of T-pCMV-neo.</p><p><b>CONCLUSIONS</b>It showed that DC transfected by p53 gene could induce potent HLA-A(2) restrictive CTL to kill tumor cell efficiently.</p>


Subject(s)
Humans , Antigens, CD , B7-2 Antigen , CD40 Antigens , Cell Line, Tumor , Allergy and Immunology , Coculture Techniques , Cytotoxicity, Immunologic , Allergy and Immunology , Dendritic Cells , Allergy and Immunology , Metabolism , Granulocyte-Macrophage Colony-Stimulating Factor , Pharmacology , Interleukin-4 , Pharmacology , Membrane Glycoproteins , T-Lymphocytes , Allergy and Immunology , Tumor Suppressor Protein p53 , Genetics , Physiology
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