Tuch B E, Jones A, Turtle J R
Diabetologia. 1985 Jan;28(1):28-31. doi: 10.1007/BF00276996.
The release of insulin from the human pancreas in response to glucose is known to be either poor or absent in the fetus, whereas in the infant and adult, the response is much greater. The maturation of this response was examined systematically in this study using pancreases that were initially obtained at 14-20 weeks gestation and maintained either in culture alone or by passaging them in diabetic nude mice. Stimulation with glucose was carried out in vitro using tissue of ages ranging from 14 to 58 weeks. A response to glucose was initially seen at 25 weeks and this dramatically increased in the fetal tissue that had reached an age of 55 weeks or more. One of the nude mice used for passage developed normoglycaemia and when the pancreatic implant of age 52 weeks was removed, diabetes recurred. Our findings support the idea of the use of human fetal pancreatic tissue in the treatment of diabetes mellitus.
已知胎儿对葡萄糖的反应是,人胰腺释放胰岛素的能力很差或根本没有,而在婴儿和成人中,这种反应要大得多。在本研究中,使用最初在妊娠14 - 20周时获得的胰腺,将其单独培养或在糖尿病裸鼠体内传代,系统地研究了这种反应的成熟过程。使用14至58周龄的组织在体外进行葡萄糖刺激。最初在25周时观察到对葡萄糖的反应,并且在达到55周龄或更大年龄的胎儿组织中这种反应显著增加。用于传代的一只裸鼠出现了正常血糖,当移除52周龄的胰腺植入物时,糖尿病复发。我们的研究结果支持使用人胎儿胰腺组织治疗糖尿病的观点。