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Hierarchical and cybernetic nature of biologic systems and their relevance to homeostatic adaptation to low-level exposures to oxidative stress-inducing agents.

机译:生物系统的层级和控制论性质及其与体内适应水平的适应性以适应低水平暴露于氧化应激诱导剂。

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摘要

During evolution in an aerobic environment, multicellular organisms survived by adaptive responses to both the endogenous oxidative metabolism in the cells of the organism and the chemicals and low-level radiation to which they had been exposed. The defense repertoire exists at all levels of the biological hierarchy--from the molecular and biochemical level to the cellular and tissue level to the organ and organ system level. Cells contain preventive antioxidants to suppress oxidative damage to membranes. Cells also contain proteins and DNA; built-in redundancies for damaged molecules and organelles; tightly coupled redox systems; pools of reductants; antioxidants; DNA repair mechanisms and sensitive sensor molecules such as nuclear factor kappa beta; and signal transduction mechanisms affecting both transcription and post-translational modification of proteins needed to cope with oxidative stress. The biologic consequences of the low-level radiation that exceeds the background level of oxidative damage could be necrosis or apoptosis, cell proliferation, or cell differentiation. These effects are triggered by oxidative stress-induced signal transduction mechanisms--an epigenetic, not genotoxic, process. If the end points of cell proliferation, differentiation, or cell death are not seen at frequencies above background levels in an organism, it is unlikely that low-level radiation would play a role in the multistep processes of chronic diseases such as cancer. The mechanism linked to homeostatic regulation of proliferation and adaptive functions in a multicellular organism could provide protection of any one cell receiving deposited energy by the radiation tract through the sharing of reductants and by triggering apoptosis of target stem cells. Examples of the role of gap junctional intercellular communication in the adaptive response of cells and the bystander effect illustrate how the interaction of cells can modulate the effect of radiation on the single cell.
机译:在有氧环境中进化过程中,多细胞生物通过对生物细胞中的内源性氧化代谢以及它们所接触的化学物质和低水平辐射的适应性反应而存活下来。从分子和生化水平到细胞和组织水平再到器官和器官系统水平,防御库存在于生物等级的各个级别。细胞含有预防性的抗氧化剂,以抑制对膜的氧化损伤。细胞还含有蛋白质和DNA。内置的冗余用于损坏的分子和细胞器;紧密耦合的氧化还原系统;还原剂池;抗氧化剂; DNA修复机制和敏感的传感器分子,例如核因子κβ;信号转导机制会影响蛋白质的转录和翻译后修饰,以应对氧化应激。低水平辐射超过背景水平的氧化损伤的生物学后果可能是坏死或凋亡,细胞增殖或细胞分化。这些效应是由氧化应激诱导的信号转导机制触发的-一种表观遗传而非遗传毒性过程。如果在生物体中高于背景水平的频率看不到细胞增殖,分化或细胞死亡的终点,则低水平辐射不太可能在诸如癌症等慢性疾病的多步过程中发挥作用。与多细胞生物体内的稳态调节增殖和适应功能有关的机制可以通过共享还原剂并触发靶干细胞凋亡来保护任何一个通过辐射束接收沉积能量的细胞。间隙连接细胞间通讯在细胞适应性反应中的作用和旁观者效应的例子说明了细胞相互作用如何调节辐射对单个细胞的作用。

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