Hudacova Erika, Abaffy Pavel, Kaplan Mehmet Mahsum, Krausova Michaela, Kubista Mikael, Machon Ondrej
Department of Developmental Biology, Institute of Experimental Medicine, Czech Academy of Sciences, Videnska 1083, 14200 Prague, Czech Republic; Department of Cell Biology, Faculty of Science, Charles University, Vinicna 7, 12000 Prague, Czech Republic.
Laboratory of Gene Expression, Institute of Biotechnology, Czech Academy of Sciences, Prumyslova 595, 25200 Vestec, Czech Republic.
Bone. 2025 Jan;190:117297. doi: 10.1016/j.bone.2024.117297. Epub 2024 Oct 24.
Craniofacial morphogenesis depends on complex cell fate decisions during the differentiation of post-migratory cranial neural crest cells. Molecular mechanisms of cell differentiation of mesenchymal cells to developing bones, cartilage, teeth, tongue, and other craniofacial tissues are still poorly understood. We performed single-cell transcriptomic analysis of craniofacial mesenchymal cells derived from cranial NCCs in mouse embryo. Using FACS sorting of Wnt1-Cre2 progeny, we carefully mapped the cell heterogeneity in the craniofacial region during the initial stages of cartilage and bone formation. Transcriptomic data and in vivo validations identified molecular determinants of major cell populations involved in the development of lower and upper jaw, teeth, tongue, dermis, or periocular mesenchyme. Single-cell transcriptomic analysis of Meis2-deficient mice revealed critical gene expression differences, including increased osteogenic and cell adhesion markers. This leads to affected mesenchymal cell differentiation and increased ossification, resulting in impaired bone, cartilage, and tongue formation.
颅面形态发生取决于迁移后颅神经嵴细胞分化过程中复杂的细胞命运决定。间充质细胞分化为发育中的骨骼、软骨、牙齿、舌头和其他颅面组织的分子机制仍知之甚少。我们对来自小鼠胚胎颅神经嵴细胞的颅面间充质细胞进行了单细胞转录组分析。通过对Wnt1-Cre2后代进行荧光激活细胞分选(FACS),我们仔细绘制了软骨和骨形成初始阶段颅面区域的细胞异质性图谱。转录组数据和体内验证确定了参与上下颌、牙齿、舌头、真皮或眼周间充质发育的主要细胞群的分子决定因素。对Meis2基因缺陷小鼠的单细胞转录组分析揭示了关键的基因表达差异,包括成骨和细胞粘附标志物的增加。这导致间充质细胞分化受影响和骨化增加,从而导致骨骼、软骨和舌头形成受损。