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자료유형
학술저널
저자정보
저널정보
대한생화학·분자생물학회 Experimental and Molecular Medicine Experimental and Molecular Medicine 제37권 제4호
발행연도
2005.1
수록면
335 - 342 (8page)

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Cell cycle regulating proteins are known to have close relation with the proliferation of the mammal-ian cells. In injured liver, the number of HSCs is increased from proliferation. However, the ex-pression of cell cycle proteins of HSCs during proliferation remains unevaluated. Therefore, cell cycle protein profiles of HSCs were studied in dimethyl-nitrosamine (DMN)-induced rat liver fi-brosis model. Sprague-Dawley rats were intraperi-toneally injected of DMN and the animals were sacrificed every week up to 4 weeks. HSCs were separated and the number of the cells in S phase was counted to evaluate the cell proliferation by flow cytometry. The expression of cyclin A, cyclin B, cyclin D1, cdk2, cdk4, cdc2, proliferating cell nuclear antigen (PCNA), p21 Cip/WAF1 , and p27 was examined with immunoblotting analysis. Portion of S-phase cells peaked 7days after DMN injection. At that time, cyclin A, and PCNA showed significant increase in HSCs compared to untreated HSCs (114% and 116%, respectively, P <0.001). p21 Cip/WAF1 was decreased significantly in DMN-treated HSCs com -pared to control cells (88%, P <0.001). The increase of cyclin A, and PCNA and the decrease of p21 Cip/WAF1 seem to play important roles in the proliferation of HSCs during the early period of DMN treatment.

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