Suppr超能文献

严肃的纤毛:一个微小的细胞器照亮了进化、疾病和细胞间通讯。

Seriously cilia: A tiny organelle illuminates evolution, disease, and intercellular communication.

机构信息

Department of Biochemistry and Biophysics, Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, USA.

Department of Biochemistry and Biophysics, Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, USA; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.

出版信息

Dev Cell. 2023 Aug 7;58(15):1333-1349. doi: 10.1016/j.devcel.2023.06.013. Epub 2023 Jul 24.

Abstract

The borders between cell and developmental biology, which have always been permeable, have largely dissolved. One manifestation is the blossoming of cilia biology, with cell and developmental approaches (increasingly complemented by human genetics, structural insights, and computational analysis) fruitfully advancing understanding of this fascinating, multifunctional organelle. The last eukaryotic common ancestor probably possessed a motile cilium, providing evolution with ample opportunity to adapt cilia to many jobs. Over the last decades, we have learned how non-motile, primary cilia play important roles in intercellular communication. Reflecting their diverse motility and signaling functions, compromised cilia cause a diverse range of diseases collectively called "ciliopathies." In this review, we highlight how cilia signal, focusing on how second messengers generated in cilia convey distinct information; how cilia are a potential source of signals to other cells; how evolution may have shaped ciliary function; and how cilia research may address thorny outstanding questions.

摘要

细胞生物学和发育生物学之间的界限一直是相互渗透的,现在已经基本消失。其中一个表现是纤毛生物学的蓬勃发展,细胞和发育方法(越来越多地辅以人类遗传学、结构见解和计算分析)成功地加深了对这个迷人的多功能细胞器的理解。最后一个真核生物的共同祖先可能拥有一个能动的纤毛,为进化提供了充足的机会使纤毛适应许多工作。在过去的几十年里,我们已经了解了非能动的、初级纤毛在细胞间通讯中发挥的重要作用。反映出它们多样的运动和信号功能,纤毛功能障碍会导致一系列被称为“纤毛病”的疾病。在这篇综述中,我们强调了纤毛信号的方式,重点介绍了在纤毛中产生的第二信使如何传递不同的信息;纤毛如何成为向其他细胞传递信号的潜在来源;进化可能如何塑造纤毛功能;以及纤毛研究如何解决棘手的悬而未决的问题。

相似文献

1
Seriously cilia: A tiny organelle illuminates evolution, disease, and intercellular communication.
Dev Cell. 2023 Aug 7;58(15):1333-1349. doi: 10.1016/j.devcel.2023.06.013. Epub 2023 Jul 24.
2
Tectonic Proteins Are Important Players in Non-Motile Ciliopathies.
Cell Physiol Biochem. 2018;50(1):398-409. doi: 10.1159/000494017. Epub 2018 Oct 4.
3
Ciliopathies and the Kidney: A Review.
Am J Kidney Dis. 2021 Mar;77(3):410-419. doi: 10.1053/j.ajkd.2020.08.012. Epub 2020 Oct 9.
4
Genes and molecular pathways underpinning ciliopathies.
Nat Rev Mol Cell Biol. 2017 Sep;18(9):533-547. doi: 10.1038/nrm.2017.60. Epub 2017 Jul 12.
5
Interplay between primary cilia, ubiquitin-proteasome system and autophagy.
Biochimie. 2019 Nov;166:286-292. doi: 10.1016/j.biochi.2019.06.009. Epub 2019 Jun 15.
6
Appearing and disappearing acts of cilia.
J Biosci. 2023;48(1). doi: 10.1007/s12038-023-00326-6.
7
Live cell imaging of dynamic behaviors of motile cilia and primary cilium.
Microscopy (Oxf). 2019 Apr 1;68(2):99-110. doi: 10.1093/jmicro/dfy147.
8
Primary cilia and signaling pathways in mammalian development, health and disease.
Nephron Physiol. 2009;111(3):p39-53. doi: 10.1159/000208212. Epub 2009 Mar 10.

引用本文的文献

1
Primary cilia and BBS4 are required for postnatal pituitary development.
bioRxiv. 2025 Jul 18:2025.07.15.664994. doi: 10.1101/2025.07.15.664994.
2
Foxn3 is required to suppress aberrant ciliogenesis in nonphotoreceptor retinal neurons.
Proc Natl Acad Sci U S A. 2025 Jul 22;122(29):e2500871122. doi: 10.1073/pnas.2500871122. Epub 2025 Jul 15.
4
Pharmaceutical inhibition of the Chk2 kinase mitigates cone photoreceptor degeneration in an iPSC model of Bardet-Biedl syndrome.
iScience. 2025 Mar 1;28(4):112130. doi: 10.1016/j.isci.2025.112130. eCollection 2025 Apr 18.
6
Physiologic mechanisms underlying polycystic kidney disease.
Physiol Rev. 2025 Jul 1;105(3):1553-1607. doi: 10.1152/physrev.00018.2024. Epub 2025 Feb 12.
7
Cholesterol ensures ciliary polycystin-2 localization to prevent polycystic kidney disease.
Life Sci Alliance. 2025 Feb 3;8(4). doi: 10.26508/lsa.202403063. Print 2025 Apr.
8
Characterization of the Cystic Phenotype Associated with Monoallelic ALG8 and ALG9 Pathogenic Variants.
J Am Soc Nephrol. 2025 Jun 1;36(6):1056-1071. doi: 10.1681/ASN.0000000613. Epub 2025 Feb 3.
10
Motile Cilia in Female and Male Reproductive Tracts and Fertility.
Cells. 2024 Nov 28;13(23):1974. doi: 10.3390/cells13231974.

本文引用的文献

1
An RFX transcription factor regulates ciliogenesis in the closest living relatives of animals.
Curr Biol. 2023 Sep 11;33(17):3747-3758.e9. doi: 10.1016/j.cub.2023.07.022. Epub 2023 Aug 7.
2
Shedding of ciliary vesicles at a glance.
J Cell Sci. 2022 Oct 1;135(19). doi: 10.1242/jcs.246553. Epub 2022 Oct 12.
3
A PKA inhibitor motif within SMOOTHENED controls Hedgehog signal transduction.
Nat Struct Mol Biol. 2022 Oct;29(10):990-999. doi: 10.1038/s41594-022-00838-z. Epub 2022 Oct 6.
4
Disruption of Dopamine Receptor 1 Localization to Primary Cilia Impairs Signaling in Striatal Neurons.
J Neurosci. 2022 Aug 31;42(35):6692-6705. doi: 10.1523/JNEUROSCI.0497-22.2022.
5
Grey wolf genomic history reveals a dual ancestry of dogs.
Nature. 2022 Jul;607(7918):313-320. doi: 10.1038/s41586-022-04824-9. Epub 2022 Jun 29.
6
The Intimate Connection Between Lipids and Hedgehog Signaling.
Front Cell Dev Biol. 2022 Jun 9;10:876815. doi: 10.3389/fcell.2022.876815. eCollection 2022.
8
The Joubert-Meckel-Nephronophthisis Spectrum of Ciliopathies.
Annu Rev Genomics Hum Genet. 2022 Aug 31;23:301-329. doi: 10.1146/annurev-genom-121321-093528. Epub 2022 Jun 2.
9
Reflections on the past, present and future of developmental biology.
Dev Biol. 2022 Aug;488:30-34. doi: 10.1016/j.ydbio.2022.05.001. Epub 2022 May 10.
10
Amphibian mucus triggers a developmental transition in the frog-killing chytrid fungus.
Curr Biol. 2022 Jun 20;32(12):2765-2771.e4. doi: 10.1016/j.cub.2022.04.006. Epub 2022 Apr 25.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验