Adair-Kirk T L, Cox K H, Cox J V
Department of Microbiology and Immunology, University of Tennessee Health Science Center, 858 Madison Avenue, Memphis, Tennessee 38163, USA.
J Cell Biol. 1999 Dec 13;147(6):1237-48. doi: 10.1083/jcb.147.6.1237.
The variant chicken kidney AE1 anion exchangers differ only at the NH(2) terminus of their cytoplasmic domains. Transfection studies have indicated that the variant chicken AE1-4 anion exchanger accumulates in the basolateral membrane of polarized MDCK kidney epithelial cells, while the AE1-3 variant, which lacks the NH(2)-terminal 63 amino acids of AE1-4, primarily accumulates in the apical membrane. Mutagenesis studies have shown that the basolateral accumulation of AE1-4 is dependent upon two tyrosine residues at amino acids 44 and 47 of the polypeptide. Interestingly, either of these tyrosines is sufficient to direct efficient basolateral sorting of AE1-4. However, in the absence of both tyrosine residues, AE1-4 accumulates in the apical membrane of MDCK cells. Pulse-chase studies have shown that after delivery to the cell surface, newly synthesized AE1-4 is recycled to the Golgi where it acquires additional N-linked sugar modifications. This Golgi recycling activity is dependent upon the same cytoplasmic tyrosine residues that are required for the basolateral sorting of this variant transporter. Furthermore, mutants of AE1-4 that are defective in Golgi recycling are unable to associate with the detergent insoluble actin cytoskeleton and are rapidly turned over. These studies, which represent the first description of tyrosine-dependent cytoplasmic sorting signal for a type III membrane protein, have suggested a critical role for the actin cytoskeleton in regulating AE1 anion exchanger localization and stability in this epithelial cell type.
变异的鸡肾AE1阴离子交换蛋白仅在其细胞质结构域的氨基末端有所不同。转染研究表明,变异的鸡AE1-4阴离子交换蛋白积聚在极化的MDCK肾上皮细胞的基底外侧膜中,而缺少AE1-4氨基末端63个氨基酸的AE1-3变异体则主要积聚在顶端膜中。诱变研究表明,AE1-4在基底外侧的积聚依赖于该多肽第44和47位氨基酸处的两个酪氨酸残基。有趣的是,这两个酪氨酸中的任何一个都足以指导AE1-4在基底外侧的有效分选。然而,在没有这两个酪氨酸残基的情况下,AE1-4会积聚在MDCK细胞的顶端膜中。脉冲追踪研究表明,新合成的AE1-4在被转运到细胞表面后,会被循环回高尔基体,在那里它会获得额外的N-连接糖修饰。这种高尔基体循环活性依赖于该变异转运蛋白在基底外侧分选中所需的相同细胞质酪氨酸残基。此外,在高尔基体循环中存在缺陷的AE1-4突变体无法与去污剂不溶性肌动蛋白细胞骨架结合,并会迅速被降解。这些研究首次描述了III型膜蛋白的酪氨酸依赖性细胞质分选信号,表明肌动蛋白细胞骨架在调节这种上皮细胞类型中AE1阴离子交换蛋白的定位和稳定性方面起着关键作用。