Lavický J, Lopez M Gonzalez, Chochola V, Kompaníková P, Rakultsev V, Raška J, Winchester E Wentworth, Tuaima H, Englmaier L, Verner J, Švandová E, Buchtová M, Cotney J, Bryja V, Bohačiaková D, Bárta T, Krivanek J
Department of Histology and Embryology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Department of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech Republic.
J Dent Res. 2025 Jul 12:220345251348148. doi: 10.1177/00220345251348148.
The molecular mechanisms controlling the differentiation of stem cells into specialized cells and tissues are enormously complex. Deciphering the mechanisms behind this precisely regulated process is essential not only for understanding ontogenesis but also for interpretations of evolutionary dynamics. A deep understanding of differentiation processes in various cell types would open the way for safe and targeted tissue engineering. This was previously limited by technical constraints, but the recent development of multiomic approaches has overcome these barriers, providing unprecedented insight into the intricate workings of this molecular machinery. Based on single-cell RNA-seq analyses of continuously growing mouse teeth, 4 transcription factors (, , , and ) were selected. Their role during tooth development has not been previously evaluated. Here, we provide evidence about their function in the differentiation of odontoblasts-dental cells responsible for dentin production. Our results revealed that controlled overexpression of specific transcription factors directly in mouse-induced pluripotent stem cells is sufficient to guide their differentiation into cells with an odontoblast-like phenotype, both in vitro and in vivo. The differentiated cells exhibited upregulated expression of odontoblast-specific molecular markers (DMP1 and DSP) as well as production of collagenous and mineralized tissue. We demonstrate that a deep insight into fundamental developmental events can provide a powerful basis for innovative cell differentiation approaches. Taken together, this research might serve as a proof of concept for using large-omics data in the generation of specific, differentiated cell types by controlled expression of a particular transcription factor code. This may represent a turning point in both developmental biology and regenerative medicine fields.
控制干细胞分化为特定细胞和组织的分子机制极其复杂。破解这一精确调控过程背后的机制不仅对于理解个体发育至关重要,而且对于解释进化动态也必不可少。深入了解各种细胞类型中的分化过程将为安全且有针对性的组织工程开辟道路。这在以前受到技术限制,但多组学方法的最新发展克服了这些障碍,为深入了解这种分子机制的复杂运作提供了前所未有的视角。基于对持续生长的小鼠牙齿的单细胞RNA测序分析,选择了4种转录因子(、、、和)。它们在牙齿发育过程中的作用此前尚未得到评估。在这里,我们我们我们提供了它们在成牙本质细胞(负责牙本质生成的牙细胞)分化中功能的证据。我们的结果表明,直接在小鼠诱导多能干细胞中对特定转录因子进行可控的过表达足以在体外和体内引导它们分化为具有成牙本质细胞样表型的细胞。分化后的细胞表现出成牙本质细胞特异性分子标记物(DMP1和DSP)的表达上调以及胶原组织和矿化组织的产生。我们证明,对基本发育事件的深入洞察可以为创新的细胞分化方法提供有力依据。综上所述,这项研究可能为通过特定转录因子代码的可控表达利用大数据组学数据生成特定的分化细胞类型提供概念验证。这可能代表着发育生物学和再生医学领域的一个转折点。