Yiu S C, Lambert R W, Bradley M E, Ingham C E, Hales K L, Wood R L, Mircheff A K
Department of Physiology and Biophysics, University of Southern California, School of Medicine, Los Angeles 90033.
J Membr Biol. 1988 Jun;102(3):185-94. doi: 10.1007/BF01925712.
To test the possibility that stimulation of secretion leads Na,K-ATPase to be recruited from cytoplasmic pools and inserted into basal-lateral plasma membranes, we surveyed the subcellular distributions of Na,K-ATPase in resting and stimulated fragments of rat exorbital lacrimal gland. After a two-dimensional separation procedure based on differential sedimentation and density gradient centrifugation, we defined six density windows, which differ from one another in their contents of biochemical markers. The membranes equilibrating in window I could be identified as a sample of basal-lateral membranes; in resting preparations these membranes contained Na,K-ATPase enriched 16.6-fold with respect to the initial homogenates. Windows II through VI contained various cytoplasmic membrane populations; these accounted for roughly 80% of the total recovered Na,K-ATPase activity. Thirty-minute stimulation with 10 microM carbachol caused a 1.4-fold increase (P less than 0.05) in the total Na,K-ATPase content of window I; this increase could be largely accounted for by a 1.7-fold decrease in the total Na,K-ATPase content of density window V. Acid phosphatase activity also redistributed following stimulation, but it was recruited from a different source, and it was inserted into membranes equilibrating in windows II and III as well as into the membranes of window I.
为了验证分泌刺激是否会使钠钾ATP酶从细胞质池募集并插入基底外侧质膜,我们研究了大鼠眶外泪腺静止和刺激片段中钠钾ATP酶的亚细胞分布。在基于差速沉降和密度梯度离心的二维分离程序后,我们定义了六个密度窗口,它们在生化标记物含量上彼此不同。在窗口I达到平衡的膜可被鉴定为基底外侧膜样本;在静止制剂中,这些膜所含的钠钾ATP酶相对于初始匀浆富集了16.6倍。窗口II至VI包含各种细胞质膜群体;这些占回收的总钠钾ATP酶活性的约80%。用10微摩尔卡巴胆碱刺激30分钟导致窗口I中总钠钾ATP酶含量增加1.4倍(P小于0.05);这种增加很大程度上可由密度窗口V中总钠钾ATP酶含量下降1.7倍来解释。酸性磷酸酶活性在刺激后也发生了重新分布,但它是从不同来源募集的,并插入到在窗口II和III达到平衡的膜以及窗口I的膜中。