Upadhyai Priyanka, Guleria Vishal Singh, Udupa Prajna
Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, Karnataka, India.
PeerJ. 2020 Aug 21;8:e9799. doi: 10.7717/peerj.9799. eCollection 2020.
Primary cilia are non-motile sensory antennae present on most vertebrate cell surfaces. They serve to transduce and integrate diverse external stimuli into functional cellular responses vital for development, differentiation and homeostasis. Ciliary characteristics, such as length, structure and frequency are often tailored to distinct differentiated cell states. Primary cilia are present on a variety of skeletal cell-types and facilitate the assimilation of sensory cues to direct skeletal development and repair. However, there is limited knowledge of ciliary variation in response to the activation of distinct differentiation cascades in different skeletal cell-types. C3H10T1/2, MC3T3-E1 and ATDC5 cells are mesenchymal stem cells, preosteoblast and prechondrocyte cell-lines, respectively. They are commonly employed in numerous in vitro studies, investigating the molecular mechanisms underlying osteoblast and chondrocyte differentiation, skeletal disease and repair. Here we sought to evaluate the primary cilia length and frequencies during osteogenic differentiation in C3H10T1/2 and MC3T3-E1 and chondrogenic differentiation in ATDC5 cells, over a period of 21 days. Our data inform on the presence of stable cilia to orchestrate signaling and dynamic alterations in their features during extended periods of differentiation. Taken together with existing literature these findings reflect the occurrence of not only lineage but cell-type specific variation in ciliary attributes during differentiation. These results extend our current knowledge, shining light on the variabilities in primary cilia features correlated with distinct differentiated cell phenotypes. It may have broader implications in studies using these cell-lines to explore cilia dependent cellular processes and treatment modalities for skeletal disorders centered on cilia modulation.
原发性纤毛是大多数脊椎动物细胞表面存在的非运动性感觉触角。它们用于将各种外部刺激转导并整合为对发育、分化和体内平衡至关重要的功能性细胞反应。纤毛的特征,如长度、结构和频率,通常根据不同的分化细胞状态进行调整。原发性纤毛存在于多种骨骼细胞类型上,并促进感觉信号的同化以指导骨骼发育和修复。然而,对于不同骨骼细胞类型中不同分化级联激活后纤毛的变化,我们了解有限。C3H10T1/2、MC3T3-E1和ATDC5细胞分别是间充质干细胞、前成骨细胞和前软骨细胞系。它们常用于众多体外研究,以探究成骨细胞和软骨细胞分化、骨骼疾病和修复背后的分子机制。在这里,我们试图评估C3H10T1/2和MC3T3-E1细胞成骨分化以及ATDC5细胞软骨分化过程中21天内原发性纤毛的长度和频率。我们的数据揭示了稳定纤毛的存在,以协调信号传导以及它们在长时间分化过程中特征的动态变化。结合现有文献,这些发现反映了分化过程中不仅存在谱系特异性,而且存在细胞类型特异性的纤毛属性变化。这些结果扩展了我们目前的知识,揭示了与不同分化细胞表型相关的原发性纤毛特征的变异性。这可能对使用这些细胞系探索纤毛依赖性细胞过程以及以纤毛调节为中心的骨骼疾病治疗方式的研究具有更广泛的意义。