Zhang Ranran, Xing Xiumei
Institute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun 130112, China.
Key Laboratory of Genetics, Breeding and Reproduction of Special Economic Animal, Ministry of Agriculture and Rural Affairs of the People's Republic of China, Changchun 130112, China.
Int J Mol Sci. 2025 Mar 14;26(6):2642. doi: 10.3390/ijms26062642.
Antlers, as the only fully regenerable bone tissue in mammals, serve as an exceptional model for investigating bone growth, mineralization, articular cartilage repair, and the pathophysiology of osteoporosis. Nevertheless, the exact molecular mechanisms governing osteogenesis, particularly the dynamic cellular interactions and signaling pathways coordinating these processes, remain poorly characterized. This study used single-cell RNA sequencing (scRNA-seq) on the 10× Genomics Chromium platform, combined with bulk-RNA sequencing results, to comprehensively analyze molecular regulatory mechanisms in rapid antler osteogenesis. The results showed that eight cell types were identified in sika deer antler during the growth and ossification stages: mesenchymal, chondrocyte, osteoblast, pericyte, endothelial, monocyte/macrophage, osteoclast, and NK cells. Chondrocytes were predominantly found during the growth stage, while osteoblasts were more abundant during the ossification stage. Mesenchymal cells were subclassified into three subcategories: MSC_1 ( and ), MSC_2 (, ), and MSC_3 ( and ). MSC_3 was predominantly present during the growth stage. During the growth stage, MSC_1 and MSC_2 upregulated genes related to vasculature development (, ) and cell differentiation (, ). During the ossification stage, these subcategories upregulated genes involved in the positive regulation of p53 class mediator signal transduction (, , , and ), osteoblast differentiation (, , ), and proton-motive ATP synthesis (, , , ). Endothelial cells were categorized into five subpopulations: Enc_1 (, ), Enc_2 (), Enc_3 (, ), Enc_4 (, ), and Enc_5 (, ). Combined scRNA-seq and bulk RNA-seq analysis revealed that the ossification stage's upregulation genes included osteoclast- and endothelial cell-specific genes, while the growth stage's upregulation genes were mainly linked to collagen organization, osteoblast differentiation, mitotic cell cycle, and chondrocyte differentiation. Overall, this study offers a detailed single-cell analysis of gene expression patterns in antlers during the growth and ossification stages, providing insights into the molecular mechanisms driving rapid osteogenesis.
鹿角作为哺乳动物中唯一能完全再生的骨组织,是研究骨生长、矿化、关节软骨修复以及骨质疏松症病理生理学的一个特殊模型。然而,调控成骨作用的确切分子机制,尤其是协调这些过程的动态细胞相互作用和信号通路,仍未得到充分表征。本研究在10×基因组学铬平台上使用单细胞RNA测序(scRNA-seq),结合批量RNA测序结果,全面分析快速鹿茸成骨过程中的分子调控机制。结果表明,在梅花鹿鹿茸的生长和骨化阶段鉴定出了八种细胞类型:间充质细胞、软骨细胞、成骨细胞、周细胞、内皮细胞、单核细胞/巨噬细胞、破骨细胞和自然杀伤细胞。软骨细胞主要在生长阶段被发现,而成骨细胞在骨化阶段更为丰富。间充质细胞被细分为三个亚类:MSC_1(和)、MSC_2(、)和MSC_3(和)。MSC_3主要在生长阶段出现。在生长阶段,MSC_1和MSC_2上调了与血管发育(、)和细胞分化(、)相关的基因。在骨化阶段,这些亚类上调了参与p53类介质信号转导的正调控(、、、和)、成骨细胞分化(、、)和质子动力ATP合成(、、、)的基因。内皮细胞被分为五个亚群:Enc_1(、)、Enc_2()、Enc_3(、)、Enc_4(、)和Enc_5(、)。综合scRNA-seq和批量RNA-seq分析表明,骨化阶段上调的基因包括破骨细胞和内皮细胞特异性基因,而生长阶段上调的基因主要与胶原蛋白组织、成骨细胞分化、有丝分裂细胞周期和软骨细胞分化有关。总体而言,本研究对鹿茸生长和骨化阶段的基因表达模式进行了详细的单细胞分析,为驱动快速成骨的分子机制提供了见解。