Tse J S, Shibayama Y, Lin B J
Histochemistry. 1978 Dec 13;58(4):297-305. doi: 10.1007/BF00495386.
With a cytochemical method using guanylyl imidodiphosphate as a substrate, the guanylate cyclase activity was localized on the plasma membrane of A, B and D cells of islets of Langerhans isolated from the rat. Adequate control experiments were performed by a double-blind method. Parallel biochemical assay showed that guanylate cyclase activity was not completely lost after fixation with 1% glutaraldehyde and incubation with 4 mM lead nitrate. Furthermore, the depressed activity was still stimulatable with acetylcholine.
采用以鸟苷酰亚胺二磷酸为底物的细胞化学方法,将鸟苷酸环化酶活性定位在从大鼠分离的胰岛A、B和D细胞的质膜上。通过双盲法进行了充分的对照实验。平行生化分析表明,用1%戊二醛固定并与4 mM硝酸铅孵育后,鸟苷酸环化酶活性并未完全丧失。此外,降低的活性仍可被乙酰胆碱刺激。