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        west china medical publishers
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        find Author "ZHENG Qian" 2 results
        • Construction of Transgenic Animal Expression Vector of Mouse Thyroid Transcription Factor-2 and Its Expression in Bone Marrow-derived Mesenchymal Stem Cells

          目的 構建小鼠甲狀腺轉錄因子-2(TTF-2)轉基因動物表達載體(pBROAD3-TTF-2),觀察其在小鼠骨髓間充質干細胞(BMSC)中的表達。 方法 從C57BL/6J小鼠肝臟組織中提取基因組DNA,利用聚合酶鏈式反應方法擴增出TTF-2基因1 113 bp開放閱讀框,通過DNA重組技術將TTF-2基因片段插入克隆載體pMD18-T中,經測序正確后,再重組于pBROAD3-mcs中,構建轉基因動物表達載體pBROAD3-TTF-2,用酶切電泳分析對其進行鑒定。運用脂質體轉染試劑將其轉染BMSC后,蛋白質印跡法檢測TTF-2基因的表達。 結果 ① DNA測序證實目的基因序列正確無突變,酶切電泳分析得到相應的目的片段,大小與理論計算值一致,成功構建轉基因動物表達載體pBROAD3-TTF-2。② 蛋白質印跡法顯示轉染的BMSC高表達TTF-2蛋白。 結論 成功構建了pBROAD3- TTF-2轉基因動物表達載體,顯示其轉染BMSC后TTF-2基因的表達,為下一步建立TTF-2轉基因小鼠模型奠定了基礎。

          Release date:2016-09-07 02:33 Export PDF Favorites Scan
        • Effect of Kartogenin combined with adipose-derived stem cells on tendon-bone healing after anterior cruciate ligament reconstruction

          Objective To investigate the effect of Kartogenin (KGN) combined with adipose-derived stem cells (ADSCs) on tendon-bone healing after anterior cruciate ligament (ACL) reconstruction in rabbits. Methods After the primary ADSCs were cultured by passaging, the 3rd generation cells were cultured with 10 μmol/L KGN solution for 72 hours. The supernatant of KGN-ADSCs was harvested and mixed with fibrin glue at a ratio of 1∶1; the 3rd generation ADSCs were mixed with fibrin glue as a control. Eighty adult New Zealand white rabbits were taken and randomly divided into 4 groups: saline group (group A), ADSCs group (group B), KGN-ADSCs group (group C), and sham-operated group (group D). After the ACL reconstruction model was prepared in groups A-C, the saline, the mixture of ADSCs and fibrin glue, and the mixture of supernatant of KGN-ADSCs and fibrin glue were injected into the tendon-bone interface and tendon gap, respectively. ACL was only exposed without other treatment in group D. The general conditions of the animals were observed after operation. At 6 and 12 weeks, the tendon-bone interface tissues and ACL specimens were taken and the tendon-bone healing was observed by HE staining, c-Jun N-terminal kinase (JNK) immunohistochemical staining, and TUNEL apoptosis assay. The fibroblasts were counted, and the positive expression rate of JNK protein and apoptosis index (AI) were measured. At the same time point, the tensile strength test was performed to measure the maximum load and the maximum tensile distance to observe the biomechanical properties. Results Twenty-eight rabbits were excluded from the study due to incision infection or death, and finally 12, 12, 12, and 16 rabbits in groups A-D were included in the study, respectively. After operation, the tendon-bone interface of groups A and B healed poorly, while group C healed well. At 6 and 12 weeks, the number of fibroblasts and positive expression rate of JNK protein in group C were significantly higher than those of groups A, B, and D (P<0.05). Compared with 6 weeks, the number of fibroblasts gradually decreased and the positive expression rate of JNK protein and AI decreased in group C at 12 weeks after operation, with significant differences (P<0.05). Biomechanical tests showed that the maximum loads at 6 and 12 weeks after operation in group C were higher than in groups A and B, but lower than those in group D, while the maximum tensile distance results were opposite, but the differences between groups were significant (P<0.05). Conclusion After ACL reconstruction, local injection of a mixture of KGN-ADSCs and fibrin glue can promote the tendon-bone healing and enhance the mechanical strength and tensile resistance of the tendon-bone interface.

          Release date:2023-08-09 01:37 Export PDF Favorites Scan
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