Takács-Vellai Krisztina, Vellai Tibor, Farkas Zsolt, Mehta Anil
Department of Biological Anthropology, Eötvös Loránd University, Pázmány Péter stny. 1/C, 1117, Budapest, Hungary,
Cell Mol Life Sci. 2015 Apr;72(8):1447-62. doi: 10.1007/s00018-014-1803-0. Epub 2014 Dec 24.
In textbooks of biochemistry, nucleoside diphosphate conversion to a triphosphate by nucleoside diphosphate 'kinases' (NDPKs, also named NME or NM23 proteins) merits a few lines of text. Yet this essential metabolic function, mediated by a multimeric phosphotransferase protein, has effects that lie beyond a simple housekeeping role. NDPKs attracted more attention when NM23-H1 was identified as the first metastasis suppressor gene. In this review, we examine these NDPK enzymes from a developmental perspective because of the tractable phenotypes found in simple animal models that point to common themes. The data suggest that NDPK enzymes control the availability of surface receptors to regulate cell-sensing cues during cell migration. NDPKs regulate different forms of membrane enclosure that engulf dying cells during development. We suggest that NDPK enzymes have been essential for the regulated uptake of objects such as bacteria or micronutrients, and this evolutionarily conserved endocytic function contributes to their activity towards the regulation of metastasis.
在生物化学教科书中,核苷二磷酸通过核苷二磷酸“激酶”(NDPK,也称为NME或NM23蛋白)转化为三磷酸核苷,只需寥寥数语。然而,这种由多聚体磷酸转移酶蛋白介导的基本代谢功能,其作用远不止于简单的维持细胞正常功能。当NM23-H1被鉴定为首个转移抑制基因时,NDPK受到了更多关注。在本综述中,我们从发育的角度研究这些NDPK酶,因为在简单动物模型中发现的易于处理的表型指向了共同的主题。数据表明,NDPK酶控制表面受体的可用性,以在细胞迁移过程中调节细胞感知信号。NDPK在发育过程中调节吞噬死亡细胞的不同形式的膜包被。我们认为,NDPK酶对于诸如细菌或微量营养素等物质的调控摄取至关重要,这种进化上保守的内吞功能有助于它们对转移的调控活性。