Palmiter R D, Cole T B, Findley S D
Howard Hughes Medical Institute, University of Washington, Seattle 98195-7370, USA.
EMBO J. 1996 Apr 15;15(8):1784-91.
A cDNA encoding a second zinc transporter (ZnT-2) was isolated from a rat kidney cDNA expression library by complementation of a zinc-sensitive BHK cell line. The protein predicted from the open reading frame of ZnT-2 cDNA has 359 amino acids and initiates with a CTG codon. It resembles ZnT-1 (a plasma membrane protein that stimulates zinc efflux) in overall topology in that it has six membrane-spanning domains, a histidine-rich intracellular loop and a long C-terminal tail; however, the overall amino acid identity is only 26%. Unlike ZnT-1, which is in the plasma membrane and lowers cellular zinc by stimulating zinc efflux, ZnT-2 is localized on vesicles and allows the zinc-sensitive BHK cells to accumulate zinc to levels that are much higher than non-transformed cells can tolerate. Zinc was visualized within these vesicles with zinquin, a zinc-specific fluorescent probe. The intracellular compartment that accumulates zinc is acidic as revealed by staining with acridine orange or LysoTracker. Prolonged exposure of cells expressing ZnT-2 to zinc causes an accretion of intracellular vesicles. We suggest that ZnT-2 protects these cells from zinc toxicity by facilitating zinc transport into an endosomal/lysosomal compartment.
通过对锌敏感的BHK细胞系进行互补,从大鼠肾脏cDNA表达文库中分离出一种编码第二种锌转运蛋白(ZnT-2)的cDNA。从ZnT-2 cDNA的开放阅读框预测的蛋白质有359个氨基酸,起始密码子为CTG。它在整体拓扑结构上与ZnT-1(一种刺激锌外流的质膜蛋白)相似,具有六个跨膜结构域、一个富含组氨酸的细胞内环和一条长的C末端尾巴;然而,整体氨基酸同一性仅为26%。与位于质膜并通过刺激锌外流降低细胞内锌含量的ZnT-1不同,ZnT-2定位于囊泡上,并使对锌敏感的BHK细胞能够将锌积累到远高于未转化细胞所能耐受的水平。用锌特异性荧光探针锌喹检测到这些囊泡内有锌。用吖啶橙或溶酶体追踪染料染色显示,积累锌的细胞内区室呈酸性。将表达ZnT-2的细胞长时间暴露于锌会导致细胞内囊泡增多。我们认为,ZnT-2通过促进锌转运到内体/溶酶体区室来保护这些细胞免受锌毒性的影响。