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在腺苷酸激酶7缺陷的纤毛上皮中,中心粒缺陷是原发性纤毛运动障碍表型的基础。

Centriolar defects underlie a primary ciliary dyskinesia phenotype in an adenylate kinase 7 deficient ciliated epithelium.

作者信息

Sheridan Jennifer, Grata Aline, Dorr Julia, Suva Eve E, Bresteau Enzo, Mitchell Linus R, Hassan Osama, Mitchell Brian

机构信息

Northwestern University, Feinberg School of Medicine, Department of Cell and Developmental Biology, USA.

Northwestern University, Feinberg School of Medicine, Department of Cell and Developmental Biology, USA; Northwestern University, Lurie Cancer Center, USA.

出版信息

Dev Biol. 2025 Aug;524:152-161. doi: 10.1016/j.ydbio.2025.05.011. Epub 2025 May 15.

Abstract

The skin of Xenopus embryos contains numerous multiciliated cells (MCCs), which collectively generate a directed fluid flow across the epithelial surface essential for distributing the overlaying mucous. MCCs develop into highly specialized cells to generate this flow, containing approximately 150 evenly spaced centrioles that give rise to motile cilia. MCC-driven fluid flow can be impaired when ciliary dysfunction occurs, resulting in primary ciliary dyskinesia (PCD) in humans. Mutations in a large number of genes (∼50) have been found to be causative to PCD. Recently, studies have linked low levels of Adenylate Kinase 7 (AK7) gene expression to patients with PCD; however, the mechanism for this link remains unclear. Additionally, AK7 mutations have been linked to multiple PCD patients. Adenylate kinases modulate ATP production and consumption, with AK7 explicitly associated with motile cilia. Here we reproduce an AK7 PCD-like phenotype in Xenopus and describe the cellular consequences that occur with manipulation of AK7 levels. We show that AK7 localizes throughout the cilia in a DPY30 domain-dependent manner, suggesting a ciliary function. Additionally, we find that AK7 overexpression increases centriole number, suggesting a role in regulating centriole biogenesis. We find that in AK7-depleted embryos, cilia number, length, and beat frequency are all reduced, which in turn significantly decreases the tissue-wide mucociliary flow. Additionally, we find a decrease in centriole number and an increase in sub-apical centrioles, implying that AK7 influences both centriole biogenesis and docking, which we propose underlie its defect in ciliogenesis. We find that both the AK domain and the DPY30 domain are required for proper centriole regulation. We propose that AK7 plays a role in PCD by impacting centriole biogenesis and apical docking, ultimately leading to ciliogenesis defects that impair mucociliary clearance.

摘要

非洲爪蟾胚胎的皮肤含有大量多纤毛细胞(MCCs),这些细胞共同产生跨上皮表面的定向液流,这对于分布覆盖其上的黏液至关重要。MCCs发育成高度特化的细胞以产生这种液流,含有大约150个均匀间隔的中心粒,这些中心粒产生运动性纤毛。当纤毛功能障碍发生时,MCC驱动的液流可能受损,导致人类原发性纤毛运动障碍(PCD)。已发现大量基因(约50个)的突变是PCD的病因。最近,研究将腺苷酸激酶7(AK7)基因表达水平低与PCD患者联系起来;然而,这种联系的机制仍不清楚。此外,AK7突变与多名PCD患者有关。腺苷酸激酶调节ATP的产生和消耗,AK7与运动性纤毛明确相关。在这里,我们在非洲爪蟾中重现了类似AK7 PCD的表型,并描述了操纵AK7水平时发生的细胞后果。我们表明,AK7以依赖DPY30结构域的方式定位于整个纤毛,提示其具有纤毛功能。此外,我们发现AK7过表达会增加中心粒数量,提示其在调节中心粒生物发生中起作用。我们发现,在AK7缺失的胚胎中,纤毛数量、长度和摆动频率均降低,这反过来又显著降低了全组织的黏液纤毛流动。此外,我们发现中心粒数量减少,顶端下中心粒增加,这意味着AK7影响中心粒生物发生和对接,我们认为这是其在纤毛发生中缺陷的基础。我们发现AK结构域和DPY30结构域对于正确的中心粒调节都是必需的。我们提出,AK7通过影响中心粒生物发生和顶端对接在PCD中起作用,最终导致纤毛发生缺陷,损害黏液纤毛清除功能。

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