Schwizer R W
Life Sci. 1984 Aug 13;35(7):783-8. doi: 10.1016/0024-3205(84)90348-5.
The ability of the principal islet cell types to maintain their differentiated function in vitro was assessed in a tissue culture system using neonatal rat pancreata. The effects of tissue dissociation and culture on the yield of islet tissue was measured at various times during the preparation and maintenance of cultures for 8 days. As estimated by the radioimmunoassay of insulin, glucagon and somatostatin in tissue extracts, the amount of islet tissue available for culture was reduced 50-70% following dissociation; an additional loss occurred after the first day in vitro. Only the insulin content of the tissue increased during culture. The hormone content of the media indicated that B-, A- and D-cell function was maintained throughout the culture period. The concentrations of insulin and glucagon in the medium approximately doubled and somatostatin increased 3-fold. This system has been shown to be a useful tool for the simultaneous study of the three major islet cell types and their secretory products.
在一个使用新生大鼠胰腺的组织培养系统中,评估了主要胰岛细胞类型在体外维持其分化功能的能力。在培养物制备和维持8天的不同时间,测量了组织解离和培养对胰岛组织产量的影响。根据组织提取物中胰岛素、胰高血糖素和生长抑素的放射免疫测定估计,解离后可用于培养的胰岛组织量减少了50 - 70%;在体外培养的第一天后又有额外损失。培养期间只有组织中的胰岛素含量增加。培养基中的激素含量表明,B细胞、A细胞和D细胞的功能在整个培养期都得以维持。培养基中胰岛素和胰高血糖素的浓度大约翻倍,生长抑素增加了3倍。该系统已被证明是同时研究三种主要胰岛细胞类型及其分泌产物的有用工具。