Fritz B A, Lowe A W
Department of Medicine, Stanford University, California 94305-5487, USA.
Am J Physiol. 1996 Jan;270(1 Pt 1):G176-83. doi: 10.1152/ajpgi.1996.270.1.G176.
The major zymogen granule membrane protein in the exocrine pancreas is glycoprotein 2 (GP2), a glycosyl phosphatidylinositol (GPI)-linked membrane protein. Despite its GPI anchor, GP2 is secreted into the pancreatic duct. We examined the mechanism underlying the secretion of GP2 in isolated pancreatic acini and transfected Madin-Darby canine kidney (MDCK) cells (MDCK-GP2). MDCK-GP2 cells release GP2 almost exclusively (> 95%) from the apical membrane. Using GP2 as a model, we defined a novel mechanism of polarized protein secretion in which a secretory protein is targeted via a GPI anchor to the apical plasma membrane, whereupon the mature form is released by proteolysis. Furthermore, we described two features of MDCK cells that enhance the polarized release of GP2: an apical plasma membrane-restricted distribution of the protease responsible for GP2 membrane cleavage, and a transcytotic pathway to reroute basolateral plasma membrane GP2 to the apical cell surface.
外分泌胰腺中的主要酶原颗粒膜蛋白是糖蛋白2(GP2),一种糖基磷脂酰肌醇(GPI)连接的膜蛋白。尽管GP2有GPI锚定,但它仍会分泌到胰管中。我们研究了分离的胰腺腺泡和转染的犬肾Madin-Darby细胞(MDCK)(MDCK-GP2)中GP2分泌的潜在机制。MDCK-GP2细胞几乎完全(>95%)从顶端膜释放GP2。以GP2为模型,我们定义了一种新的极化蛋白分泌机制,即分泌蛋白通过GPI锚定靶向顶端质膜,随后成熟形式通过蛋白水解释放。此外,我们描述了MDCK细胞增强GP2极化释放的两个特征:负责GP2膜切割的蛋白酶在顶端质膜的限制性分布,以及将基底外侧质膜GP2重新路由到顶端细胞表面的转胞吞途径。