胚胎器官植入成体动物:干细胞体内培养的模型?

V. Coulic, V. N. Novikov, F. Mboti, P. Delrée
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引用次数: 0

摘要

背景:目前干细胞移植越来越发达,作为成人器官移植的替代和补充解决方案应用于临床,因为提供这些干预措施的需求和能力不断增长,而缺乏供体是专利。但是,干细胞的使用仍然存在一些限制(例如,在体外从干细胞中获得的工程组织和类器官在受体体内的整合)。利用胚胎器官植入成年动物可能是干细胞发育的体内研究和评估宿主参与这一过程的另一种选择。本工作的目的是尝试不同的胚胎器官植入成年动物(第一部分),并评估它们在修复某些成年器官实验性病变中的应用(第二部分)。材料和方法:第一部分:在650多个大鼠和小鼠实验中,提出了不同的胚胎器官同基因植入部位。生理(电活动、运动和分泌活动)和形态学(照度、超声和磁成像、光学和电子显微镜)方法用于长达12个月的种植体发育评估。第二部分:对38只大鼠和29只大鼠进行了食道环形缺损和心脏热损伤修复的胎儿心脏和胎儿消化器官的检测。胎儿胰腺植入试验是在链脲佐菌素和/或蛋白质缺陷诱导的糖尿病大鼠和一小部分糖尿病患者中进行的。结果:第一部分:在“去分化”阶段之后,胎儿器官植入物可以按照个体发生模式生长,但至少在我们的实验条件下,其中一些器官不能重新组织成一个完整的功能成人器官。考虑了促进或限制类器官形成的因素。第二部分:胎儿心脏植入物增强心脏病变形态和功能修复。胎儿食管、胃或肠碎片联合壳聚糖瓣确保卵状或节段性切除后食管壁完全恢复。胚胎胰腺植入能够逆转链脲佐菌素诱导的糖尿病,并预防大鼠蛋白质剥夺后的慢性葡萄糖紊乱。在患者中发现了暂时的积极影响。结论:同种异体成体移植不同胎儿器官可能为体内干细胞分化和类器官生长的理论研究提供了一个有价值的模型。耳植入部位值得特别注意。一些有趣的应用是可能的,值得讨论和开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FOETAL Organ Implantation into Adult Animals: A Model for In vivo Culture of Stem Cells?
Background: Presently stem cell implantations are more and more developed and applied in clinics as alternative and complementary solutions to adult organ transplantation because of the growing demand and capacities to provide these interventions, while lack of donors is patent. But some limitations of stem cell use remain (for instance integration within the recipient organism of engineered tissues and organoids obtained in vitro from stem cells). The use of foetal organ implantation into adult animals may be an alternative for in vivo study of stem cell development and evaluation of the host participation to this process. The objectives of this work were to try different foetal organ implantations into adult animals (part I) and to evaluate their use for repairing experimental lesions of some adult organs (part II). Material and Methods: Part I: In > 650 experiments on rats and mice, different sites of foetal organ syngeneic implantation were proposed. Physiological (electric activity, motor and secretion activity) and morphological (per illumination, ultra sound and magnetic imaging, optic and electron microscopy) methods were used for implant development evaluation during up to 12 months. Part II: Foetal heart and foetal digestive organs were tested for both oesophagus circular defect and heart thermic lesion repair (38 and 29 rats).Trials with foetal pancreas implantation were provided in rats with diabetes induced by Streptozotocin and/or protein deficit and in a small pilot group of diabetic patients. Result: Part I: After a “dedifferentiation” phase, foetal organ implants could grow following ontogenetic pattern but – at least in our experimental conditions - some of them were not able to re-organize as a whole functional adult organ. The factors enhancing or limiting the organoid formation are considered. Part II: Foetal heart implants were proved to enhance heart lesion morphological and functional repair. Foetal oesophagus, stomach or intestine fragments combined with chitosan flaps ensured a complete restoration of the oesophagus wall after oval or segmental resection. Implantation of foetal pancreas was able to reverse Streptozotocin induced diabetes and to prevent chronic glucose disorders following protein deprivation in rats. In patients temporary positive influence was noted. Conclusion: Implantation of different foetal organs into syngeneic adults may constitute a valuable model for theoretical studies of in vivo stem cell differentiation and organoid growth. The ear implantation site deserves special attention. Some interesting applications are possible and worthwhile to be discussed and developed.
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