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Metals and cellular signaling in mammalian cells.

机译:哺乳动物细胞中的金属和细胞信号传导。

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A number of heavy metals are known to be essential for life, but most of these can also be toxic to cells under certain circumstances, or at elevated levels. Metals can directly induce gene expression through the actions of metal-responsive transcription factors. However, metals can also influence the response to non-metal extracellular signals. Cells respond to extracellular signals through a variety of different, but often interacting, signal transduction pathways. Metals can alter cell behaviour by interacting with transcription factors and transduction molecules, many of which are dependent on metals (primarily zinc) for their action. In addition, metals can affect cells in more nonspecific ways, for example, by inducing a generalized stress response or by cross-linking cell surface thiol groups. The prominent role of zinc in signal transduction combined with low intracellular free zinc levels has lead to the speculation that cellular signaling and gene expression may be regulated, in part, by zinc bioavailability. Experimental modification of the levels of the intracellular metal-binding protein, metallothionein (MT), results in altered responsiveness to extracellular signals. This observation suggests that MT is capable of influencing gene expression, perhaps by regulating the level of intracellular free zinc.
机译:已知许多重金属是生命必不可少的,但大多数重金属在某些情况下或水平升高时也会对细胞产生毒性。金属可以通过金属响应转录因子的作用直接诱导基因表达。但是,金属也会影响对非金属细胞外信号的响应。细胞通过各种不同但经常相互作用的信号转导途径对细胞外信号作出反应。金属可通过与转录因子和转导分子相互作用来改变细胞行为,其中许多转录因子和转导分子的作用依赖于金属(主要是锌)。另外,金属可以以更非特异性的方式影响细胞,例如通过诱导普遍的应激反应或通过交联细胞表面硫醇基团。锌在信号转导中的突出作用与低的细胞内游离锌水平相结合,导致人们推测细胞信号和基因表达可能部分受锌生物利用度的调节。对细胞内金属结合蛋白金属硫蛋白(MT)水平进行实验性修饰,导致对细胞外信号的响应性发生改变。该观察结果表明MT可能通过调节细胞内游离锌的水平来影响基因表达。

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