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首页> 外文期刊>Journal of Cell Science >THE IN VIVO ROLE OF ANNEXIN VII (SYNEXIN) - CHARACTERIZATION OF AN ANNEXIN VII-DEFICIENT DICTYOSTELIUM MUTANT INDICATES AN INVOLVEMENT IN CA2+-REGULATED PROCESSES
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THE IN VIVO ROLE OF ANNEXIN VII (SYNEXIN) - CHARACTERIZATION OF AN ANNEXIN VII-DEFICIENT DICTYOSTELIUM MUTANT INDICATES AN INVOLVEMENT IN CA2+-REGULATED PROCESSES

机译:膜联蛋白VII(SYNEXIN)的体内作用-膜联蛋白VII缺乏的双歧杆菌突变体的表征指示参与CA2 +调控的过程

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Dictyostelium discoideum cells harbor two annexin VII isoforms of 47 and 51 kDa which are present throughout development. In immunofluorescence and cell fractionation studies annexin VII was found in the cytoplasm and on the plasma membrane. In gene disruption mutants lacking both annexin VII isoforms growth, pinocytosis, phagocytosis, chemotaxis and motility were not significantly impaired under routine laboratory conditions, and the cells were able to complete the developmental cycle on bacterial plates. On non-nutrient agar plates development was delayed by three to four hours and a significant number of aggregates was no longer able to form fruiting bodies. Exocytosis as determined by measuring extracellular cAMP phosphodiesterase, alpha-fucosidase and alpha-mannosidase activity was unaltered, the total amounts of these enzymes were however lower in the mutant than in the wild type. The mutant cells were markedly impaired when they were exposed to low Ca2+ concentrations by adding EGTA to the nutrient medium. Under these conditions growth, motility and chemotaxis were severely affected. The Ca2+ concentrations were similar in mutant and wild-type cells both under normal and Ca2+ limiting conditions; however, the distribution was altered under low Ca2+ conditions in SYN- cells. The data suggest that annexin VII is not required for membrane fusion events but rather contributes to proper Ca2+ homeostasis in the cell. [References: 74]
机译:盘基网柄菌细胞具有两个47和51 kDa的膜联蛋白VII同工型,它们在整个发育过程中都存在。在免疫荧光和细胞分离研究中,在细胞质和质膜上发现膜联蛋白VII。在基因破坏突变体中,缺少膜联蛋白VII亚型的生长,在常规实验室条件下,胞吞,吞噬,趋化性和运动性均未受到显着损害,并且细胞能够在细菌平板上完成发育周期。在非营养琼脂平板上,发育被延迟了三到四个小时,并且大量的聚集体不再能够形成子实体。通过测量细胞外cAMP磷酸二酯酶,α-岩藻糖苷酶和α-甘露糖苷酶活性确定的胞吐作用没有改变,但是这些酶的总量在突变体中比在野生型中低。通过向营养培养基中添加EGTA,当突变细胞暴露于低Ca2 +浓度时,其受损显着。在这些条件下,生长,运动性和趋化性受到严重影响。在正常和Ca2 +限制条件下,突变型和野生型细胞中的Ca2 +浓度均相似。但是,在低Ca2 +条件下SYN-细胞的分布发生了变化。数据表明膜联蛋白事件不需要膜联蛋白VII,而是有助于细胞内适当的Ca2 +稳态。 [参考:74]

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