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创建细胞内结构域:神经元中肌动蛋白和原肌球蛋白亚型的空间隔离

Creating intracellular structural domains: spatial segregation of actin and tropomyosin isoforms in neurons.

作者信息

Gunning P, Hardeman E, Jeffrey P, Weinberger R

机构信息

Oncology Research Unit, New Children's Hospital, Parramatta, New South Wales, Australia.

出版信息

Bioessays. 1998 Nov;20(11):892-900. doi: 10.1002/(SICI)1521-1878(199811)20:11<892::AID-BIES4>3.0.CO;2-D.

Abstract

Actin microfilaments play a direct role in a variety of cell processes. Distinct populations of microfilaments are associated with different cellular compartments, such as growth cones, filipodia, stress fibers, and lamellipodia. It is becoming clear that these different populations are often composed of different isoforms of the two core microfilament components, actin and tropomyosin. This is particularly true in neurons, where actin and tropomyosin isoforms are segregated into different intracellular compartments which correspond to functionally distinct regions of the neuron. Developmental regulation of this isoform sorting suggests a specific role for some isoforms in growth and for others in stabilization of neuronal structure. This provides a mechanism by which a neuron can create and independently regulate intracellular domains composed of microfilaments with different functional properties.

摘要

肌动蛋白微丝在多种细胞过程中发挥直接作用。不同群体的微丝与不同的细胞区室相关,如生长锥、丝状伪足、应力纤维和片状伪足。越来越明显的是,这些不同群体通常由两种核心微丝成分(肌动蛋白和原肌球蛋白)的不同异构体组成。在神经元中尤其如此,其中肌动蛋白和原肌球蛋白异构体被分隔到不同的细胞内区室,这些区室对应于神经元功能上不同的区域。这种异构体分选的发育调控表明,一些异构体在生长中起特定作用,而另一些异构体在神经元结构的稳定中起作用。这提供了一种机制,通过该机制神经元可以创建并独立调节由具有不同功能特性的微丝组成的细胞内结构域。

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