Okumura K, Tojyo Y, Kanazawa M
Department of Oral Surgery (1st division) School of Dentistry, Higashi-Nippon-Gakuen University, Hokkaido, Japan.
Arch Oral Biol. 1990;35(8):677-9. doi: 10.1016/0003-9969(90)90036-a.
In parotid acini, microfilaments were predominantly localized at the luminal border when visualized with the fluorescent probe, rhodamine-phalloidin. There was no fluorescence in the cytoplasm. When acini were stimulated by isoprenaline, the membranes of the secretory granules appeared to become undercoated by microfilaments immediately after fusion with the luminal membrane. The intensity of fluorescence was correlated with the extent of enlargement of the lumina. These findings indicate that the microfilament system (actin-myosin contractile system) may play a role in regulating the movement of the luminal plasma membrane rather than in the control of transport and access of secretory granules to the lumen.
在用荧光探针罗丹明-鬼笔环肽观察时,腮腺腺泡中的微丝主要定位于管腔边界。细胞质中无荧光。当腺泡受到异丙肾上腺素刺激时,分泌颗粒的膜在与管腔膜融合后立即似乎被微丝覆盖。荧光强度与管腔扩大程度相关。这些发现表明,微丝系统(肌动蛋白-肌球蛋白收缩系统)可能在调节管腔质膜的运动中起作用,而不是在控制分泌颗粒向管腔的转运和进入中起作用。