Dudek R W, Lawrence I E
Department of Anatomy and Cell Biology, School of Medicine, East Carolina University, Greenville, NC 27858-4354.
Diabetes. 1988 Jul;37(7):891-900. doi: 10.2337/diab.37.7.891.
First, tissue recombinants were used to determine the residual capability of adult endodermal pancreatic ductal epithelium to form islets. Second, adult epithelium was challenged by placing it between adult stroma and fetal mesenchyme to investigate the epithelial response (subsequently called challenge grafts). Trypsin was used to isolate adult mouse (heteroplastic) or rat (homoplastic) pancreatic ductal epithelium and fetal rat mesenchyme. All the adult epithelium was maximally stressed with alloxan to control for beta-cell contamination. Fetal mesenchyme was layered with epithelium in vitro for at least 48 h. Subsequently, the recombinants were grafted into nude mice and allowed to develop for 4-6 wk. To assess development, grafts were removed and fixed for both light and electron microscopy. In general, the grafts became organized into vesicles, tubules, and buds, many of which were in the form of vascularized isletlike structures. Epithelium responded with mitosis and intercellular adhesion. the range of cytodifferentiation varied. Culture time, age, and adhesiveness of the fetal mesenchyme and the amount of adult epithelium used in making the recombinants influenced the degree of differentiation. Analysis of fine structure of isletlike structures revealed cells with small electron-dense granules. These observations provide evidence for activation of endodermal epithelium taken from an adult mammal.
首先,利用组织重组体来确定成年内胚层胰腺导管上皮形成胰岛的剩余能力。其次,将成年上皮置于成年基质和胎儿间充质之间,以研究上皮反应(随后称为挑战性移植)。用胰蛋白酶分离成年小鼠(异种移植)或大鼠(同种移植)的胰腺导管上皮和胎儿大鼠间充质。所有成年上皮都用四氧嘧啶进行最大程度应激处理,以控制β细胞污染。胎儿间充质在体外与上皮分层至少48小时。随后,将重组体移植到裸鼠体内并使其发育4至6周。为了评估发育情况,取出移植体并固定以进行光镜和电镜观察。一般来说,移植体组织形成囊泡、小管和芽,其中许多呈血管化的胰岛样结构形式。上皮通过有丝分裂和细胞间黏附做出反应。细胞分化的范围各不相同。培养时间、年龄、胎儿间充质的黏附性以及制备重组体时所用成年上皮的量影响分化程度。对胰岛样结构精细结构的分析揭示了具有小的电子致密颗粒的细胞。这些观察结果为成年哺乳动物来源的内胚层上皮的激活提供了证据。