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第46卷第10期           段学诚,孟 艳. 过氧化物还原酶4蛋白在衰老小鼠卵巢颗粒细胞中的核转位研究[J].
                 2026年10月                    南京医科大学学报(自然科学版),2026,46(10):1450-1456                     ·1455 ·


                A   20       ***            2.5       ***  ***       2.5                      8        ***
                   relative experssion  15  ***  ***  ***  relative experssion  2.0  *  *  relative experssion  2.0  *  ***  ***  relative experssion  6 4  ***  ***  ***

                                            1.5
                                                                     1.5
                    10
                                            1.0
                                                                     1.0
                   IL⁃1α  5 0              IL⁃1β 0.5 0              IL⁃6 0.5 0               IL⁃8  2 0
                        0  50 125 250 500        0  50 125 250 500        0  50 125 250 500      0  50 125 250 500
                      Tg concentration(nmol/L)  Tg concentration(nmol/L)  Tg concentration(nmol/L)  Tg concentration(nmol/L)
                B         Tg(nmol/L)          2.0                    2.0                     2.5
                       0  50 125 250 500      1.5                    1.5                     2.0
                                             P16/GAPDH  1.0         P21/GAPDH  1.0          P53/GAPDH
                   P16                16 kDa                                                 1.5
                   P21                21 kDa  0.5                    0.5                     1.0
                   P53                53 kDa                                                 0.5
                                               0                       0                      0
                GAPDH                 36 kDa       0  50 125 250 500      0  50 125 250 500      0  50 125 250 500
                                                  Concentration(nmol/L)  Concentration(nmol/L)  Concentration(nmol/L)
                   C
                            Control  Tg (125 nmol/L)  2.5    *            2.0     *            3      **
                        P16            16 kDa        2.0                  1.5
                                                    P16/GAPDH            P21/GAPDH  1.0       P53/GAPDH
                        P21            21 kDa        1.5                                       2
                        P53            53 kDa        1.0                  0.5                  1
                     GAPDH             36 kDa        0.5
                                                      0                    0                   0
                                                         Control Tg           Control  Tg         Control  Tg
                   A:mRNA expression levels of SASP⁃related genes IL⁃1α,IL⁃1β,IL⁃6 and IL⁃8 after treatment with different concentrations of Tg for 24 h(n=4).
                                     *
                                            ***
                Compared with the control group,P < 0.05, P < 0.001. B:Protein expression levels of P16,P21,and P53 after treatment with different concentrations
                                                                                                             *
                of Tg for 24 h. C:Protein expression levels of P16,P21,and P53 after treatment with 125 nmol/L Tg for 24 h(n=4). Compared with control group,P <
                      **
                0.05 and P < 0.01.
                                               图3 Tg诱导的KGN细胞衰老模型的验证
                                       Figure 3 Validation of Tg⁃induced KGN cell senescence model

                                     Cytosol  Nucleus            4                   3      **
                                                                PRDX4/GAPDH  2       PRDX4/Lamin B1
                                    Control Tg Control Tg        3      **
                              PRDX4                  30 kDa                          2
                             Lamin B1                66 kDa      1                   1

                              GAPDH                  36 kDa      0                   0
                                                                    Control Tg          Control  Tg
                   The distribution of PRDX4 in cytoplasm and nuclear components was detected by Western blot after nucleoplasm separation. Lamin B1 was the
                internal reference of nuclear protein and GAPDH was the internal reference of cytoplasmic protein. Relative quantitative analysis of cytoplasmic/nuclear
                                                                   **
                PRDX4 was performed on the right side(n=4). Compared with the control group,P < 0.01.
                                              图4 衰老KGN细胞中PRDX4核转位的影响
                                    Figure 4  Effect of PRDX4 nuclear translocation in senescent KGN cells

                   Author’s Contributions:
                                                                 [参考文献]
                   Duan Xuecheng was responsible for experimental operation,
                                                                 [1] Wang B S,Han J,Elisseeff J H,et al. The senescence⁃
                data analysis and manuscript writing and modification. Meng
                                                                       associated secretory phenotype and its physiological and
                Yan was responsible for the guidance of the research process,
                                                                       pathological implications[J]. Nat Rev Mol Cell Biol,
                the review and revision of the manuscript,the supervision of all
                                                                       2024,25(12):958-978
                experimental work,the acquisition of research funds,and the
                                                                 [2] Wu C Q,Chen D,Stout M B,et al. Hallmarks of ovarian
                important revision of the final manuscript.            aging[J]. Trends Endocrinol Metab,2025,36(5):418-439
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