TonEBP 通过控制极光激酶 A 和调节中心极卫星的完整性来抑制纤毛的生成。

IF 8.2 2区 生物学 Q1 CELL BIOLOGY
Batchingis Chinbold, Hyug Moo Kwon, Raekil Park
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引用次数: 0

摘要

背景:真核细胞表面的初级纤毛是接收和传递各种细胞信号通路的感觉天线。纤毛是一种动态细胞器,在细胞分化和退出细胞周期时迅速形成。这些细胞器的缺陷会导致一组广泛的疾病,即纤毛虫病。张力反应性增强子结合蛋白(TonEBP)是一种多效应激蛋白,可介导各种生理和病理细胞反应。TonEBP 因其在适应高渗环境中的作用而闻名,据报道,原发性纤毛对高渗环境有贡献。此外,TonEBP 还参与了其他多种信号通路,如促进初级纤毛生成的 Sonic Hedgehog 和 WNT 信号通路,这表明它可能具有调控作用。然而,TonEBP与原发性纤毛形成之间的功能关系仍不清楚:方法:使用 TonEBP siRNAs 和 TonEBP-mCherry 质粒研究它们对细胞纤毛率、组装和分解过程以及调节因子的影响。血清饥饿是诱导纤毛生成的条件之一:结果:我们为 TonEBP 确定了一个新的围核定位。结果表明,TonEBP缺失可促进初级纤毛的形成,而过表达则会导致纤毛细胞数量减少。此外,TonEBP 还能控制极光激酶 A 的表达和活性,而极光激酶 A 是纤毛形成的主要负调控因子。此外,在初级纤毛组装的早期阶段,TonEBP 的过表达抑制了母中心粒中 CP110 的丢失。最后,TonEBP调节了初级纤毛形成所必需的PCM1和AZI1的定位:本研究提出了 TonEBP 作为中心粒周围蛋白的新作用,它能调节中心粒卫星成分的完整性。这种调控对纤毛形成有负面影响。对纤毛组装和分解过程的研究表明,TonEBP 作用于极光激酶 A - 组蛋白去乙酰化酶 6 信号通路的上游,影响基底体的形成,从而控制纤毛的生成。综上所述,我们的数据提出了 TonEBP 对初级纤毛组装的调节作用,而这一调节作用以前从未被描述过。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TonEBP inhibits ciliogenesis by controlling aurora kinase A and regulating centriolar satellite integrity.

Background: Primary cilia on the surface of eukaryotic cells serve as sensory antennas for the reception and transmission in various cell signaling pathways. They are dynamic organelles that rapidly form during differentiation and cell cycle exit. Defects in these organelles cause a group of wide-ranging disorders called ciliopathies. Tonicity-responsive enhancer-binding protein (TonEBP) is a pleiotropic stress protein that mediates various physiological and pathological cellular responses. TonEBP is well-known for its role in adaptation to a hypertonic environment, to which primary cilia have been reported to contribute. Furthermore, TonEBP is involved in a wide variety of other signaling pathways, such as Sonic Hedgehog and WNT signaling, that promote primary ciliogenesis, suggesting a possible regulatory role. However, the functional relationship between TonEBP and primary ciliary formation remains unclear.

Methods: TonEBP siRNAs and TonEBP-mCherry plasmids were used to examine their effects on cell ciliation rates, assembly and disassembly processes, and regulators. Serum starvation was used as a condition to induce ciliogenesis.

Results: We identified a novel pericentriolar localization for TonEBP. The results showed that TonEBP depletion facilitates the formation of primary cilia, whereas its overexpression results in fewer ciliated cells. Moreover, TonEBP controlled the expression and activity of aurora kinase A, a major negative regulator of ciliogenesis. Additionally, TonEBP overexpression inhibited the loss of CP110 from the mother centrioles during the early stages of primary cilia assembly. Finally, TonEBP regulated the localization of PCM1 and AZI1, which are necessary for primary cilia formation.

Conclusions: This study proposes a novel role for TonEBP as a pericentriolar protein that regulates the integrity of centriolar satellite components. This regulation has shown to have a negative effect on ciliogenesis. Investigations into cilium assembly and disassembly processes suggest that TonEBP acts upstream of the aurora kinase A - histone deacetylase 6 signaling pathway and affects basal body formation to control ciliogenesis. Taken together, our data proposes previously uncharacterized regulation of primary cilia assembly by TonEBP.

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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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