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模拟子宫微环境诱导大鼠胎盘间充质干细胞向子宫内膜上皮细胞方向分化的实验研究 被引量:4
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作者 李爱丽 赵飞 +2 位作者 张彤艳 马志玲 肖雅琳 《中国现代医学杂志》 CAS 北大核心 2021年第15期60-66,共7页
目的模拟子宫微环境诱导大鼠胎盘间充质干细胞(PMSCs)向子宫内膜上皮细胞方向分化。方法原代培养大鼠PMSCs及传代,绘制细胞生长曲线,制备子宫内膜条件培养液,用子宫内膜条件培养液和雌激素(β-雌二醇)进行体外诱导分化PMSCs;免疫荧光化... 目的模拟子宫微环境诱导大鼠胎盘间充质干细胞(PMSCs)向子宫内膜上皮细胞方向分化。方法原代培养大鼠PMSCs及传代,绘制细胞生长曲线,制备子宫内膜条件培养液,用子宫内膜条件培养液和雌激素(β-雌二醇)进行体外诱导分化PMSCs;免疫荧光化学法检测细胞波形蛋白和角蛋白的表达;实时荧光定量聚合酶链反应(qRT-PCR)检测上皮细胞标记细胞角蛋白7(CK-7)、细胞角蛋白18(CK-18)、细胞角蛋白19(CK-19)、上皮膜抗原(EMA)的基因表达;Western blotting检测波形蛋白和角蛋白表达量。结果实验组CK-7、CK-18、CK-19、EMA mRNA相对表达量高于对照组(P<0.05);实验组波形蛋白相对表达量低于对照组(P<0.05);实验组角蛋白相对表达量高于对照组(P<0.05)。结论使用子宫内膜诱导培养液和雌激素能够促进大鼠PMSCs向子宫内膜上皮细胞方向分化,其作用显著,体外模拟子宫微环境在PMSCs向子宫内膜上皮细胞方向分化中有着重要的作用。 展开更多
关键词 子宫微环境 骨髓间充质干细胞 子宫内膜上皮细胞 细胞分化
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Coarctation of the Aorta with Aortic Arch Hypoplasia:Midterm Outcomes of Aortic Arch Reconstruction with Autologous Pulmonary Artery Patch 被引量:3
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作者 zhi-ling ma Jun Yan +4 位作者 Shou-Jun Li Zhong-Dong Hua Fu-Xia Yan Xu Wang Qiang Wang 《Chinese Medical Journal》 SCIE CAS CSCD 2017年第23期2802-2807,共6页
Background: Coarctation of the aorta (CoA) with aortic arch hypoplasia (AAH) is a relatively common congenital heart disease in clinical practice. Nonetheless, the corrective surgical technique for infants and ch... Background: Coarctation of the aorta (CoA) with aortic arch hypoplasia (AAH) is a relatively common congenital heart disease in clinical practice. Nonetheless, the corrective surgical technique for infants and children is a clinical problem that remains controversial. In this study, we sought to evaluate the surgical effects of aortic arch (AA) reconstruction with coarctation resection and aortoplasty with autologous pulmonary artery patch for infants and young children with CoA and AAH. Methods: Between January 2009 and December 2015, a total of 22 infants and young children with CoA and AAH who underwent coarctation resection and aortoplasty with autologous pulmonary artery patch were enrolled in this study. The median age of patients was 4.5 (Q1, Q3: 2.0, 14.0) months and the median body weight was 5.75 (Q1, Q3: 4.10, 9.38) kg. All patients were diagnosed with CoA and AAH, and concomitant cardiac anomalies were corrected in one stage. Perioperative and postoperative data were collected and analyzed using the paired sample t-test. Results: No perioperative deaths occurred. No residual obstruction was detected by echocardiography. The postoperative pressure difference across the repaired segment of CoA was 14.05 ± 4.26 mmHg (1 mmHg = 0.133 kPa), which was smaller than the preoperative pressure difference (48.30 ± 15.73 mmHg; t = -10.119, P 〈 0.001). The median follow-up time was 29.0 (Q1, Q3: 15.5, 57.3) months. There was no death during the follow-up period, and all patients experienced obvious clinical improvement. Only one child underwent subsequent aortic balloon angioplasty due to restenosis. Computed tomography angiography showed that the AA morphology was smooth, with no aortic aneurysm or angulation deformity. Conclusion: AA reconstruction with coarctation resection and aortoplasty with autologous pulmonary artery patch could effectively correct CoA with AAH, and the rate of reintervention for restenosis is low. 展开更多
关键词 Aortic Arch Hypoplasia: Aortic Arch Reconstruction: Aortic Coarctation Cardiac Surgical Procedures Congenital HcartDisease
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