Deretic Jovana, Cengiz-Emek Seyma, Seyrek Ece, Firat-Karalar Elif Nur
Department of Molecular Biology and Genetics, Koç University, Istanbul, Turkey.
School of Medicine, Koç University, Istanbul, Turkey.
PLoS Biol. 2025 Jul 29;23(7):e3003313. doi: 10.1371/journal.pbio.3003313. eCollection 2025 Jul.
The primary cilium is a conserved, microtubule-based organelle that transduces signaling pathways essential for development and homeostasis. It dynamically assembles and disassembles in response to intrinsic and extrinsic stimuli while maintaining remarkable structural stability and tightly regulated length. The mechanisms underlying this stability and length control are not well understood. Here, we characterized CCDC66, a microtubule-associated protein linked to ciliopathies, as an important regulator of cilium maintenance and disassembly in mouse epithelial cells. Live imaging revealed that cilia in CCDC66-depleted cells frequently fluctuate in length and exhibit increased cilium disassembly and ectocytosis. Phenotypic rescue experiments and in vitro assays showed that microtubule stabilization activity of CCDC66 is required for these functions. Temporal proximity mapping identified potential new regulators and molecular pathways involved in cilium disassembly. Further characterization revealed actin cytoskeleton and vesicular trafficking as additional mechanisms by which CCDC66 may mediate its ciliary functions. Finally, depletion of CCDC66 compromised Hedgehog and Wnt pathway activation and disrupted epithelial cell organization and polarity in two- and three-dimensional cultures. Collectively, we showed that CCDC66 regulates both ciliary and non-ciliary processes through diverse mechanisms involving microtubules, actin, and vesicular trafficking, providing insights into the pathologies associated with CCDC66.
初级纤毛是一种保守的、基于微管的细胞器,它能转导对发育和体内平衡至关重要的信号通路。它会根据内在和外在刺激动态组装和拆卸,同时保持显著的结构稳定性和严格调控的长度。这种稳定性和长度控制的潜在机制尚不清楚。在这里,我们将CCDC66(一种与纤毛病相关的微管相关蛋白)鉴定为小鼠上皮细胞中纤毛维持和拆卸的重要调节因子。实时成像显示,CCDC66缺失细胞中的纤毛长度经常波动,并且纤毛拆卸和胞吐作用增加。表型拯救实验和体外实验表明,CCDC66的微管稳定活性是这些功能所必需的。时间邻近映射确定了参与纤毛拆卸的潜在新调节因子和分子途径。进一步的表征揭示了肌动蛋白细胞骨架和囊泡运输是CCDC66可能介导其纤毛功能的额外机制。最后,CCDC66的缺失损害了刺猬信号通路和Wnt信号通路的激活,并破坏了二维和三维培养物中上皮细胞的组织和极性。我们的研究表明,CCDC66通过涉及微管、肌动蛋白和囊泡运输的多种机制调节纤毛和非纤毛过程,为与CCDC66相关的病理学提供了见解。