单细胞转录组解析颅面形态发生过程中的成骨过程

IF 3.5 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Bone Pub Date : 2024-10-24 DOI:10.1016/j.bone.2024.117297
Erika Hudacova , Pavel Abaffy , Mehmet Mahsum Kaplan , Michaela Krausova , Mikael Kubista , Ondrej Machon
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引用次数: 0

摘要

颅面形态发生取决于颅神经嵴后迁移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细胞分化分子机制仍鲜为人知。我们对源自小鼠胚胎颅骨神经细胞的颅面间充质细胞进行了单细胞转录组分析。利用 FACS 分选 Wnt1-Cre2 后代,我们仔细绘制了软骨和骨形成初期颅面区域细胞异质性的图谱。转录组数据和体内验证确定了参与上下颌骨、牙齿、舌头、真皮或眼周间质发育的主要细胞群的分子决定因素。对Meis2缺陷小鼠进行的单细胞转录组分析发现了关键的基因表达差异,包括成骨和细胞粘附标记物的增加。这导致间充质细胞分化受到影响,骨化增加,从而影响骨骼、软骨和舌头的形成。
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Single-cell transcriptomic resolution of osteogenesis during craniofacial morphogenesis
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.
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来源期刊
Bone
Bone 医学-内分泌学与代谢
CiteScore
8.90
自引率
4.90%
发文量
264
审稿时长
30 days
期刊介绍: BONE is an interdisciplinary forum for the rapid publication of original articles and reviews on basic, translational, and clinical aspects of bone and mineral metabolism. The Journal also encourages submissions related to interactions of bone with other organ systems, including cartilage, endocrine, muscle, fat, neural, vascular, gastrointestinal, hematopoietic, and immune systems. Particular attention is placed on the application of experimental studies to clinical practice.
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