• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

谁驱动了睫状“高速公路”?

Who drives the ciliary highway?

作者信息

Malicki Jarema

机构信息

MRC Centre for Developmental and Biomedical Genetics; Department of Biomedical Science; The University of Sheffield; Sheffield, UK.

出版信息

Bioarchitecture. 2012 Jul-Aug;2(4):111-7. doi: 10.4161/bioa.21101. Epub 2012 Jul 1.

DOI:10.4161/bioa.21101
PMID:22960672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3675070/
Abstract

Cilia are protrusions on the surface of cells. They are frequently motile and function to propel cells in an aqueous environment or to generate fluid flow. Equally important is the role of immotile cilia in detecting environmental changes or in sensing extracellular signals. The structure of cilia is supported by microtubules, and their formation requires microtubule-dependent motors, kinesins, which are thought to transport both structural and signaling ciliary proteins from the cell body into the distal portion of the ciliary shaft. In multicellular organisms, multiple kinesins are known to drive ciliary transport, and frequently cilia of a single cell type require more than one kinesin for their formation and function. In addition to kinesin-2 family motors, which function in cilia of all species investigated so far, kinesins from other families contribute to the transport of signaling proteins in a tissue-specific manner. It is becoming increasingly obvious that functional relationships between ciliary kinesins are complex, and a good understanding of these relationships is essential to comprehend the basis of biological processes as diverse as olfaction, vision, and embryonic development.

摘要

纤毛是细胞表面的突出物。它们通常具有运动能力,其功能是在水环境中推动细胞或产生流体流动。同样重要的是,不动纤毛在检测环境变化或感知细胞外信号方面的作用。纤毛的结构由微管支撑,其形成需要微管依赖的马达蛋白驱动蛋白,这些驱动蛋白被认为将结构和信号纤毛蛋白从细胞体运输到纤毛轴的远端部分。在多细胞生物中,已知多种驱动蛋白驱动纤毛运输,并且通常单一细胞类型的纤毛形成和功能需要不止一种驱动蛋白。除了在迄今为止研究的所有物种的纤毛中发挥作用的驱动蛋白 -2 家族马达蛋白外,其他家族的驱动蛋白以组织特异性方式促进信号蛋白的运输。越来越明显的是,纤毛驱动蛋白之间的功能关系很复杂,充分理解这些关系对于理解嗅觉、视觉和胚胎发育等多种生物过程的基础至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d62/3675070/c34411ebfc0c/bioa-2-111-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d62/3675070/65abacc6d999/bioa-2-111-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d62/3675070/dedbc67305de/bioa-2-111-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d62/3675070/c34411ebfc0c/bioa-2-111-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d62/3675070/65abacc6d999/bioa-2-111-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d62/3675070/dedbc67305de/bioa-2-111-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d62/3675070/c34411ebfc0c/bioa-2-111-g3.jpg

相似文献

1
Who drives the ciliary highway?谁驱动了睫状“高速公路”?
Bioarchitecture. 2012 Jul-Aug;2(4):111-7. doi: 10.4161/bioa.21101. Epub 2012 Jul 1.
2
Unexpected Roles for Ciliary Kinesins and Intraflagellar Transport Proteins.纤毛驱动蛋白和鞭毛内运输蛋白的意外作用。
Genetics. 2016 Jun;203(2):771-85. doi: 10.1534/genetics.115.180943. Epub 2016 Apr 2.
3
Microtubule-depolymerizing kinesins in the regulation of assembly, disassembly, and length of cilia and flagella.微管解聚驱动蛋白在纤毛和鞭毛的组装、解聚及长度调控中的作用
Int Rev Cell Mol Biol. 2015;317:241-65. doi: 10.1016/bs.ircmb.2015.01.008. Epub 2015 Mar 5.
4
Structural Biology of Cilia and Intraflagellar Transport.纤毛与鞭毛内运输的结构生物学
Annu Rev Cell Dev Biol. 2022 Oct 6;38:103-123. doi: 10.1146/annurev-cellbio-120219-034238. Epub 2022 Jun 29.
5
Kinesin motors and primary cilia.驱动蛋白和初级纤毛。
Biochem Soc Trans. 2011 Oct;39(5):1120-5. doi: 10.1042/BST0391120.
6
Intraflagellar transport motors in cilia: moving along the cell's antenna.纤毛中的鞭毛内运输马达:沿着细胞的天线移动。
J Cell Biol. 2008 Jan 14;180(1):23-9. doi: 10.1083/jcb.200709133. Epub 2008 Jan 7.
7
CDKL kinase regulates the length of the ciliary proximal segment.CDKL 激酶调节纤毛近端节的长度。
Curr Biol. 2021 Jun 7;31(11):2359-2373.e7. doi: 10.1016/j.cub.2021.03.068. Epub 2021 Apr 14.
8
Ciliary kinesins beyond IFT: Cilium length, disassembly, cargo transport and signalling.除了内体运输颗粒蛋白(IFT)之外的纤毛驱动蛋白:纤毛长度、解聚、货物运输及信号传导
Biol Cell. 2019 Apr;111(4):79-94. doi: 10.1111/boc.201800074. Epub 2019 Feb 15.
9
Functional coordination of intraflagellar transport motors.鞭毛内运输马达的功能协调
Nature. 2005 Jul 28;436(7050):583-7. doi: 10.1038/nature03818.
10
Optimal sidestepping of intraflagellar transport kinesins regulates structure and function of sensory cilia.最佳地避开纤毛内运输运动蛋白调节感觉纤毛的结构和功能。
EMBO J. 2020 Jun 17;39(12):e103955. doi: 10.15252/embj.2019103955. Epub 2020 Apr 27.

引用本文的文献

1
Loss of Deacetylation Enzymes Hdac6 and Sirt2 Promotes Acetylation of Cytoplasmic Tubulin, but Suppresses Axonemal Acetylation in Zebrafish Cilia.去乙酰化酶Hdac6和Sirt2的缺失促进细胞质微管蛋白的乙酰化,但抑制斑马鱼纤毛中轴丝的乙酰化。
Front Cell Dev Biol. 2021 Jun 28;9:676214. doi: 10.3389/fcell.2021.676214. eCollection 2021.
2
The Phenotype of the Food-Allergic Patient.食物过敏患者的表型。
Immunol Allergy Clin North Am. 2021 May;41(2):165-175. doi: 10.1016/j.iac.2021.01.001. Epub 2021 Mar 26.
3
Identification of two early life eczema and non-eczema phenotypes with high risk for asthma development.

本文引用的文献

1
Kinesin-2 family in vertebrate ciliogenesis.脊椎动物纤毛发生中的驱动蛋白-2 家族。
Proc Natl Acad Sci U S A. 2012 Feb 14;109(7):2388-93. doi: 10.1073/pnas.1116035109. Epub 2012 Jan 30.
2
Structural insights into human Kif7, a kinesin involved in Hedgehog signalling.对参与刺猬信号通路的驱动蛋白——人类Kif7的结构洞察。
Acta Crystallogr D Biol Crystallogr. 2012 Feb;68(Pt 2):154-9. doi: 10.1107/S0907444911053042. Epub 2012 Jan 13.
3
Kinesin motors and primary cilia.驱动蛋白和初级纤毛。
鉴定具有高哮喘发展风险的两种早期生命特应性皮炎和非特应性皮炎表型。
Clin Exp Allergy. 2019 Jun;49(6):829-837. doi: 10.1111/cea.13379. Epub 2019 Mar 27.
4
Structural and molecular bases of rod photoreceptor morphogenesis and disease.视杆光感受器形态发生与疾病的结构和分子基础。
Prog Retin Eye Res. 2016 Nov;55:32-51. doi: 10.1016/j.preteyeres.2016.06.002. Epub 2016 Jun 22.
5
The V-ATPase accessory protein Atp6ap1b mediates dorsal forerunner cell proliferation and left-right asymmetry in zebrafish.V-ATP酶辅助蛋白Atp6ap1b介导斑马鱼背侧先驱细胞增殖和左右不对称性。
Dev Biol. 2015 Nov 1;407(1):115-30. doi: 10.1016/j.ydbio.2015.08.002. Epub 2015 Aug 5.
6
The roles of evolutionarily conserved functional modules in cilia-related trafficking.进化保守功能模块在纤毛相关运输中的作用。
Nat Cell Biol. 2013 Dec;15(12):1387-97. doi: 10.1038/ncb2888.
7
Kinesin-2 family motors in the unusual photoreceptor cilium.异常光感受器纤毛中的驱动蛋白-2家族马达蛋白
Vision Res. 2012 Dec 15;75:33-6. doi: 10.1016/j.visres.2012.10.008. Epub 2012 Oct 31.
Biochem Soc Trans. 2011 Oct;39(5):1120-5. doi: 10.1042/BST0391120.
4
Evolution: Tracing the origins of centrioles, cilia, and flagella.进化:追踪中心粒、纤毛和鞭毛的起源。
J Cell Biol. 2011 Jul 25;194(2):165-75. doi: 10.1083/jcb.201011152.
5
Kinesin-3 KLP-6 regulates intraflagellar transport in male-specific cilia of Caenorhabditis elegans.动力蛋白-3 KLP-6 调控秀丽隐杆线虫雄性特异性纤毛中的鞭毛内运输。
Curr Biol. 2011 Jul 26;21(14):1239-44. doi: 10.1016/j.cub.2011.06.027. Epub 2011 Jul 14.
6
A role for the primary cilium in Notch signaling and epidermal differentiation during skin development.初级纤毛在 Notch 信号传导和皮肤发育过程中的表皮分化中的作用。
Cell. 2011 Jun 24;145(7):1129-41. doi: 10.1016/j.cell.2011.05.030.
7
Centriolar kinesin Kif24 interacts with CP110 to remodel microtubules and regulate ciliogenesis.中心体驱动蛋白 Kif24 与 CP110 相互作用以重塑微管并调节纤毛发生。
Cell. 2011 Jun 10;145(6):914-25. doi: 10.1016/j.cell.2011.04.028. Epub 2011 May 27.
8
Nephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargos.肾囊蛋白和 MKS 蛋白与 IFT 颗粒相互作用,促进选定的纤毛货物的运输。
EMBO J. 2011 May 20;30(13):2532-44. doi: 10.1038/emboj.2011.165.
9
Complex interactions between genes controlling trafficking in primary cilia.控制初级纤毛运输的基因之间的复杂相互作用。
Nat Genet. 2011 Jun;43(6):547-53. doi: 10.1038/ng.832. Epub 2011 May 8.
10
Molecular motor KIF17 is fundamental for memory and learning via differential support of synaptic NR2A/2B levels.分子马达 KIF17 通过差异化支持突触 NR2A/2B 水平对记忆和学习至关重要。
Neuron. 2011 Apr 28;70(2):310-25. doi: 10.1016/j.neuron.2011.02.049.