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Barbed ends rule

机译:倒刺规则

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摘要

To explore their surroundings, cells use probes of various shapes. Whether the probes are broad and flat, or long and thin, seems to be regulated by proteins at the growing ends of actin filaments. Cells reach out with various structures as they crawland interact with their environment. Broad, flat protrusions called lamellipodia surge forward and adhere to surfaces, allowing cells to gain traction and move. Long, thin protrusions called filopodia extend several micrometres ahead of the cells, appearing to explore extracellular surfaces, sense guiding cues and direct the rest of the cell. Extension of both lamellipodia and filopodia is powered by polymerization of the structural protein actin into filaments. As the filaments lengthen, the fast-growing 'barbed' ends push the cell's boundary membrane outward. Lamellipodia protrude when the actin filaments at the leading edge are short and highly branched; by contrast, filopodia arise when the filaments are long, unbranched, and arranged in tight, parallel bundles. But given the similarities in the actin polymerization machinery that drives the two types of protrusion, what determines whether lamellipodia or filopodia form? Marisan Mejillano and colleagues, writing in Cell, report that the answer lies with proteins that control actin polymerization at the filament barbed ends.
机译:为了探索周围环境,细胞使用了各种形状的探针。探针是宽的还是扁平的,还是长而细的,似乎都受到肌动蛋白丝生长末端的蛋白质的调节。细胞在爬行并与环境互动时会伸出各种结构。宽阔,平坦的突起被称为lamellipodia,向前涌动并粘附在表面,使细胞获得牵引力并移动。长而细的突起被称为丝状伪足,在细胞之前延伸了数微米,似乎在探索细胞外表面,感知引导信号并引导细胞的其余部分。通过将结构蛋白肌动蛋白聚合成细丝,促进了lamellipodia和filopodia的延伸。随着细丝的延长,快速生长的“倒刺”端将细胞的边界膜向外推。当前缘的肌动蛋白丝短而高度分支时,Lamellipodia突出。相反,丝状体较长,不分叉且排列成紧密平行的束时,会产生丝状伪足。但是,鉴于驱动两种突出类型的肌动蛋白聚合机制的相似性,是什么决定了片状脂蛋白或丝状伪足的形式? Marisan Mejillano及其同事在《细胞》杂志上撰文指出,答案在于控制丝状带刺末端肌动蛋白聚合的蛋白质。

著录项

  • 来源
    《Nature》 |2004年第7001期|p.734-735|共2页
  • 作者

    Dorothy A. Schafer;

  • 作者单位
  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 自然科学总论;
  • 关键词

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