中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2013年
14期
2558-2562
,共5页
杨锐%马昭杰%陈容平%王梅%张振%蔡德鸿%陈宏
楊銳%馬昭傑%陳容平%王梅%張振%蔡德鴻%陳宏
양예%마소걸%진용평%왕매%장진%채덕홍%진굉
干细胞%干细胞移植%骨髓间充质干细胞%胰岛%移植%同种异体胰岛移植%免疫耐受%骨髓细胞%胰岛细胞%糖尿病小型猪模型%小型猪%国家自然科学基金%干细胞图片文章
榦細胞%榦細胞移植%骨髓間充質榦細胞%胰島%移植%同種異體胰島移植%免疫耐受%骨髓細胞%胰島細胞%糖尿病小型豬模型%小型豬%國傢自然科學基金%榦細胞圖片文章
간세포%간세포이식%골수간충질간세포%이도%이식%동충이체이도이식%면역내수%골수세포%이도세포%당뇨병소형저모형%소형저%국가자연과학기금%간세포도편문장
背景:胰岛移植为有望根治糖尿病的一种方法,而移植排斥问题阻碍了移植的开展,诱导受体对供体移植物的免疫耐受是解决同种异体移植排斥反应的关键.目的:观察骨髓间充质干细胞输注对糖尿病小型猪同种异体胰岛移植物存活时间的影响.方法:无菌条件下抽取动物骨髓,离心弃上清.取单核细胞层,洗涤后加入 L-DMEM 培养基,调整细胞浓度为1×109 L-1.培养48 h 后换液去除未贴壁的细胞,依据贴壁培养法分离和扩增间充质干细胞.取第5代细胞作为移植供源,调整细胞浓度为1×1010 L-1.四氧嘧啶制备糖尿病小型猪模型,随机分为骨髓细胞组和干细胞+骨髓细胞组,经肝门静脉分别植入胰岛细胞、骨髓细胞,胰岛细胞、骨髓细胞和骨髓间充质干细胞.结果与结论:骨髓间充质干细胞联合骨髓细胞输注较单纯骨髓细胞输注能显著延长同种异体小型猪胰岛移植物存活时间(P <0.05),同时受体血清胰岛素能较长时间维持较高水平.提示骨髓间充质干细胞输注能显著延长猪胰岛移植物存活时间,并促进胰岛移植物正常功能的发挥.
揹景:胰島移植為有望根治糖尿病的一種方法,而移植排斥問題阻礙瞭移植的開展,誘導受體對供體移植物的免疫耐受是解決同種異體移植排斥反應的關鍵.目的:觀察骨髓間充質榦細胞輸註對糖尿病小型豬同種異體胰島移植物存活時間的影響.方法:無菌條件下抽取動物骨髓,離心棄上清.取單覈細胞層,洗滌後加入 L-DMEM 培養基,調整細胞濃度為1×109 L-1.培養48 h 後換液去除未貼壁的細胞,依據貼壁培養法分離和擴增間充質榦細胞.取第5代細胞作為移植供源,調整細胞濃度為1×1010 L-1.四氧嘧啶製備糖尿病小型豬模型,隨機分為骨髓細胞組和榦細胞+骨髓細胞組,經肝門靜脈分彆植入胰島細胞、骨髓細胞,胰島細胞、骨髓細胞和骨髓間充質榦細胞.結果與結論:骨髓間充質榦細胞聯閤骨髓細胞輸註較單純骨髓細胞輸註能顯著延長同種異體小型豬胰島移植物存活時間(P <0.05),同時受體血清胰島素能較長時間維持較高水平.提示骨髓間充質榦細胞輸註能顯著延長豬胰島移植物存活時間,併促進胰島移植物正常功能的髮揮.
배경:이도이식위유망근치당뇨병적일충방법,이이식배척문제조애료이식적개전,유도수체대공체이식물적면역내수시해결동충이체이식배척반응적관건.목적:관찰골수간충질간세포수주대당뇨병소형저동충이체이도이식물존활시간적영향.방법:무균조건하추취동물골수,리심기상청.취단핵세포층,세조후가입 L-DMEM 배양기,조정세포농도위1×109 L-1.배양48 h 후환액거제미첩벽적세포,의거첩벽배양법분리화확증간충질간세포.취제5대세포작위이식공원,조정세포농도위1×1010 L-1.사양밀정제비당뇨병소형저모형,수궤분위골수세포조화간세포+골수세포조,경간문정맥분별식입이도세포、골수세포,이도세포、골수세포화골수간충질간세포.결과여결론:골수간충질간세포연합골수세포수주교단순골수세포수주능현저연장동충이체소형저이도이식물존활시간(P <0.05),동시수체혈청이도소능교장시간유지교고수평.제시골수간충질간세포수주능현저연장저이도이식물존활시간,병촉진이도이식물정상공능적발휘.
@@@@BACKGROUND: Islet transplantation is a promising method used to radical y cure diabetes mel itus. The immune rejection caused by transplantation hinders the development of transplantation. The immune tolerance of recipients to donor grafts is a key to solving the problem of al otransplantation rejection reaction. OBJECTIVE: To investigate the influence of infusion of bone marrow mesenchymal stem cel s on the survival time of islet al ograft in the minipigs after islet al otransplantation. METHODS: Under sterile condition, minipig bone marrow was taken and the supernatant was discarded after centrifugation. After washed with L-DMEM culture medium, mononuclear cel s were adjusted to be 1×109/L. After 48-hour culture, nonadherent cel s were discarded and mesenchymal stem cel s were isolated and amplified. Passage 5 cel s were taken as donors and cel concentration was adjusted to be 1×1010/L. Minipig models of al oxan-induced diabetes mel itus were prepared and then randomly divided into two groups: bone marrow cel s and bone marrow cel s + mesenchymal stem cel s. In the bone marrow cel s group, islet cel s and bone marrow cel s were infused. In the bone marrow cel s + mesenchymal stem cel s group, islet cel s, bone marrow cel s and bone marrow mesenchymal stem cel s were infused. RESULTS AND CONCLUSION: Compared with infusion of simple bone marrow cel s, infusion of bone marrow mesenchymal stem cel s and bone marrow cel s significantly prolonged the survival time of islet al ografts (P <0.05) and maintained high serum insulin level for a longer time in diabetic minipigs. These findings suggest that bone marrow mesenchymal stem cel infusion can significantly prolong the survival time of islet al ografts and contribute to the normal function of islet al ografts in diabetic minipigs.