NDP kinase can modulate contraction of Dictyostelium cytoskeletons.

C Aguado-Velasco, M Véron, J A Rambow, E R Kuczmarski
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引用次数: 5

Abstract

Extraction of Dictyostelium amoebae with Triton X-100 produces robust cytoskeletons composed mainly of actin and myosin II. These cytoskeletons rapidly contract when mixed with Mg-ATP in simple buffers. The Triton-soluble fraction was found to contain a GTP-dependent activity that prevented contraction by Mg-ATP. This activity was purified, and identified, as nucleoside diphosphate kinase (NDP kinase). The apparent inhibition resulted from pre-contraction of the cytoskeletons. Tightly bound cytoskeletal ADP was presumably phosphorylated, and the resulting ATP powered contraction. NDP kinase appeared to be unique in this capacity, since other regenerating systems did not cause pre-contraction. Reconstitution experiments demonstrated that the kinase must be in physical contact with the cytoskeleton. These results suggest that Dictyostelium NDP kinase is able to channel ATP to the myosin molecule, and this could play a role in directly regulating cytoskeletal contraction or in facilitating contraction under conditions where intracellular ATP concentrations are low. This ability to modulate cytoskeletal contraction could help to explain observations in other systems whereby defects in NDP kinase result in abnormal development or changes in the metastatic potential of cancer cells.

NDP激酶可以调节盘基骨柱细胞骨架的收缩。
用Triton X-100提取变形虫Dictyostelium amoebae可获得主要由肌动蛋白和肌球蛋白II组成的坚固的细胞骨架。当与Mg-ATP混合在简单缓冲液中时,这些细胞骨架迅速收缩。发现triton可溶性部分含有gtp依赖性活性,阻止Mg-ATP收缩。该活性被纯化并鉴定为核苷二磷酸激酶(NDP激酶)。明显的抑制是由于细胞骨架的预收缩。紧密结合的细胞骨架ADP可能被磷酸化,由此产生的ATP为收缩提供动力。NDP激酶似乎具有独特的这种能力,因为其他再生系统不会引起预收缩。重构实验表明,激酶必须与细胞骨架物理接触。这些结果表明Dictyostelium NDP激酶能够将ATP引导到肌球蛋白分子,这可能在直接调节细胞骨架收缩或在细胞内ATP浓度低的条件下促进收缩中发挥作用。这种调节细胞骨架收缩的能力可以帮助解释在其他系统中观察到的NDP激酶缺陷导致癌细胞异常发育或转移潜力改变的现象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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