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肌球蛋白重链磷酸化在盘基网柄菌运动、趋化性和F-肌动蛋白定位中的作用。

The role of myosin heavy chain phosphorylation in Dictyostelium motility, chemotaxis and F-actin localization.

作者信息

Heid Paul J, Wessels Deborah, Daniels Karla J, Gibson D Phillip, Zhang Hui, Voss Ed, Soll David R

机构信息

W. M. Keck Dynamic Image Analysis Facility, Department of Biological Sciences, The University of Iowa, Iowa City, IA 52242, USA.

出版信息

J Cell Sci. 2004 Sep 15;117(Pt 20):4819-35. doi: 10.1242/jcs.01358. Epub 2004 Aug 31.

Abstract

To assess the role of myosin II heavy chain (MHC) phosphorylation in basic motility and natural chemotaxis, the Dictyostelium mhcA null mutant mhcA(-), mhcA(-) cells rescued with a myosin II gene that mimics the constitutively unphosphorylated state (3XALA) and mhcA(-) cells rescued with a myosin II gene that mimics the constitutively phosphorylated state (3XASP), were analyzed in buffer and in response to the individual spatial, temporal and concentration components of a cAMP wave using computer-assisted methods. Each mutant strain exhibited unique defects in cell motility and chemotaxis. Although mhcA(-) cells could crawl with some polarity and showed chemotaxis with highly reduced efficiency in a spatial gradient of cAMP, they were very slow, far less polar and more three-dimensional than control cells. They were also incapable of responding to temporal gradients of cAMP, of chemotaxis in a natural wave of cAMP or streaming late in aggregation. 3XASP cells were faster and chemotactically more efficient than mhcA(-) cells, but still incapable of responding to temporal gradients of cAMP, chemotaxis in natural waves of cAMP or streaming late in aggregation. 3XALA cells were fast, were able to respond to temporal gradients of cAMP, and responded to natural waves of cAMP. However, they exhibited a 50% reduction in chemotactic efficiency, could not stream late in aggregation and could not enter the streams of control cells in mixed cultures. F-actin staining further revealed that while the presence of unphosphorylated MHC was essential for the increase in F-actin in the cytoplasm in response to the increasing temporal gradient of cAMP in the front of a natural wave, the actual dephosphorylation event was essential for the associated increase in cortical F-actin. The results of these studies indicate that MHC phosphorylation-dephosphorylation, like myosin II regulatory light chain phosphorylation-dephosphorylation, represents a potential downstream target of the regulatory cascades emanating from the different phases of the wave.

摘要

为了评估肌球蛋白II重链(MHC)磷酸化在基本运动性和天然趋化性中的作用,使用计算机辅助方法,对盘基网柄菌mhcA基因敲除突变体mhcA(-)、用模拟组成型未磷酸化状态的肌球蛋白II基因拯救的mhcA(-)细胞(3XALA)以及用模拟组成型磷酸化状态的肌球蛋白II基因拯救的mhcA(-)细胞(3XASP)在缓冲液中以及对cAMP波的各个空间、时间和浓度成分的反应进行了分析。每个突变株在细胞运动性和趋化性方面都表现出独特的缺陷。尽管mhcA(-)细胞能够以一定的极性爬行,并且在cAMP的空间梯度中表现出趋化性,但效率大大降低,它们非常缓慢,极性远低于对照细胞,且更具三维性。它们也无法对cAMP的时间梯度作出反应,无法在cAMP的天然波中进行趋化或在聚集后期进行流动。3XASP细胞比mhcA(-)细胞更快,趋化效率更高,但仍然无法对cAMP的时间梯度作出反应,无法在cAMP的天然波中进行趋化或在聚集后期进行流动。3XALA细胞速度快,能够对cAMP的时间梯度作出反应,并对cAMP的天然波作出反应。然而,它们的趋化效率降低了50%,在聚集后期无法流动,并且在混合培养中无法进入对照细胞的流中。F-肌动蛋白染色进一步显示,虽然未磷酸化的MHC的存在对于响应天然波前端cAMP时间梯度增加而导致细胞质中F-肌动蛋白增加至关重要,但实际的去磷酸化事件对于皮质F-肌动蛋白的相关增加至关重要。这些研究结果表明,MHC磷酸化-去磷酸化,与肌球蛋白II调节轻链磷酸化-去磷酸化一样,代表了来自波不同阶段的调节级联反应的潜在下游靶点。

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