Yamamoto T, Ozawa H
Arch Histol Jpn. 1977;40 Suppl:49-60. doi: 10.1679/aohc1950.40.supplement_49.
Adenylate cyclase activity in the taste buds of the papilla vallata of the tongue, in the EC cells of the duodenal mucosa and in the chromaffin cells of the adrenal medulla of the hamster was histochemically examined using the method invented by Wagner and co-workers (1972). Two types of taste bud cells were distinguished. The dark cell was characterized by a dark cytoplasm: the light cell, by a clear-looking cytoplasm. When AMP-PNP was used as a substrate, and intense activity was demonstrated along the microvilli of all cells in the taste bud. Much weaker activity was demonstrated on the lateral cell membrane. After the use of ATP, the reaction products were found rather evenly distributed over the surface of the taste bud cell. The synaptic area on the surface of the light cell, however, was devoid of reaction products. Among the several kinds of basal-granulated gut cells examined, the EC cell of the duodenal mucosa was one. An intense activity was demonstrated along the microvilli after the use of AMP-PNP. When ATP was used as a substrate, a positive reaction was demonstrated on the lateral cell membranes as well as on the luminal microvilli; the reaction on the microvilli was much stronger than that on the lateral cell membrane. The chromaffin cells of the adrenal medulla showed almost no activity with AMP-PNP. However, when ATP was used, the plasma membrane of Schwann cells and axons showed an intense reaction. The cell membrane of the adrenaline and noradrenaline-storing cells showed a slightly positive reaction. The synaptic area of chromaffin cell was always negative in the reaction. The positive adenylate cyclase activity in the gustatory cells and gut endocrine cells may have some relation to the stimulus reception. This is in keeping with the observation that adrenal medulla chromaffin cells, which were embedded in the internal milieu, did not react to adenylate cyclase.
采用瓦格纳及其同事(1972年)发明的方法,对仓鼠舌轮廓乳头味蕾、十二指肠黏膜EC细胞和肾上腺髓质嗜铬细胞中的腺苷酸环化酶活性进行了组织化学检测。区分出两种类型的味蕾细胞。暗细胞的特征是细胞质深色;亮细胞的特征是细胞质看起来清澈。当使用AMP-PNP作为底物时,味蕾中所有细胞的微绒毛上都显示出强烈的活性。在细胞外侧膜上的活性则弱得多。使用ATP后,反应产物在味蕾细胞表面分布较为均匀。然而,亮细胞表面的突触区域没有反应产物。在所检测的几种基底颗粒性肠细胞中,十二指肠黏膜的EC细胞是其中之一。使用AMP-PNP后,微绒毛上显示出强烈的活性。当使用ATP作为底物时,外侧膜和腔面微绒毛上都出现阳性反应;微绒毛上的反应比外侧膜上的反应强烈得多。肾上腺髓质的嗜铬细胞对AMP-PNP几乎没有活性。然而,当使用ATP时,施万细胞和轴突的质膜显示出强烈的反应。储存肾上腺素和去甲肾上腺素的细胞的细胞膜显示出轻微的阳性反应。嗜铬细胞的突触区域在反应中总是呈阴性。味觉细胞和肠道内分泌细胞中腺苷酸环化酶的阳性活性可能与刺激感受有某种关系。这与观察结果一致,即处于内环境中的肾上腺髓质嗜铬细胞对腺苷酸环化酶没有反应。