In the present study, the effect of blockage of the costimulatory signal CD86 at time of implantation on the expressions of TGF-β1, MMP-9, TIMP-3 and PAI-1 proteins at the maternal-fetal interface and the outcome of ...In the present study, the effect of blockage of the costimulatory signal CD86 at time of implantation on the expressions of TGF-β1, MMP-9, TIMP-3 and PAI-1 proteins at the maternal-fetal interface and the outcome of pregnancy in mufine abortion-prone model was investigated, in which the CBA/J × DBA/2 matings were used as the abortion-prone model and the CBA/J × BALB/c matings used as the normal pregnant model. The study was performed in following three groups： 2 groups of the abortion-prone model, which were experimental group and control experimental group, and 1 group of normal pregnant model, and each group had 10 pregnant CBA/J mice exclusively. Female pregnant CBA/J mice in the experimental group received an intraperitoneal （i. p. ） injection of 100μg of antimouse CD86 mAb in 200 μl of PBS at day 4.5 of gestation, and the irrelevant-isotope matched rat IgG2b was administrated in the control experimental group with the same dosage and at same time. For the normal pregnant group, no treatment was given. The pregnant CBA/J mice were killed on day 13.5 of gestation. Then, the embryo resorption rate was calculated and the expressions of TGF-β1, MMP-9, TIMP3 and PAI-1 were detected by using immunohistochemical methods. It was demonstrated that the embryo resorption rate in the experimental group was significantly reduced in comparison with that in the control experimental group （X^2 = 7.441, P = 0.006）, but there was no significant difference with that in normal pregnant group （X^2 = 0.016, P = 0.898）. The expressions of TGF-β1 and PAI-1 in the experimental group were significantly increased in comparison with that in the control experimental group （P =0.010, P = 0.003, respectively）, with no significant difference from that in the nonnal pregnant group （P = 0.500）. However, the expression of MMP-9 in the experimental group was significantly reduced in comparison with that in the control experimental group （P = 0.012） with no significant difference from that in the normal pregnant 展开更多
文摘In the present study, the effect of blockage of the costimulatory signal CD86 at time of implantation on the expressions of TGF-β1, MMP-9, TIMP-3 and PAI-1 proteins at the maternal-fetal interface and the outcome of pregnancy in mufine abortion-prone model was investigated, in which the CBA/J × DBA/2 matings were used as the abortion-prone model and the CBA/J × BALB/c matings used as the normal pregnant model. The study was performed in following three groups： 2 groups of the abortion-prone model, which were experimental group and control experimental group, and 1 group of normal pregnant model, and each group had 10 pregnant CBA/J mice exclusively. Female pregnant CBA/J mice in the experimental group received an intraperitoneal （i. p. ） injection of 100μg of antimouse CD86 mAb in 200 μl of PBS at day 4.5 of gestation, and the irrelevant-isotope matched rat IgG2b was administrated in the control experimental group with the same dosage and at same time. For the normal pregnant group, no treatment was given. The pregnant CBA/J mice were killed on day 13.5 of gestation. Then, the embryo resorption rate was calculated and the expressions of TGF-β1, MMP-9, TIMP3 and PAI-1 were detected by using immunohistochemical methods. It was demonstrated that the embryo resorption rate in the experimental group was significantly reduced in comparison with that in the control experimental group （X^2 = 7.441, P = 0.006）, but there was no significant difference with that in normal pregnant group （X^2 = 0.016, P = 0.898）. The expressions of TGF-β1 and PAI-1 in the experimental group were significantly increased in comparison with that in the control experimental group （P =0.010, P = 0.003, respectively）, with no significant difference from that in the nonnal pregnant group （P = 0.500）. However, the expression of MMP-9 in the experimental group was significantly reduced in comparison with that in the control experimental group （P = 0.012） with no significant difference from that in the normal pregnant
