Novel insights into palatal shelf elevation dynamics in normal mouse embryos.

IF 4.6 2区 生物学 Q2 CELL BIOLOGY Frontiers in Cell and Developmental Biology Pub Date : 2025-02-11 eCollection Date: 2025-01-01 DOI:10.3389/fcell.2025.1532448
Jeremy P Goering, Michael Moedritzer, Marta Stetsiv, Dona Greta Isai, Brittany M Hufft-Martinez, An J Tran, Zaid Umar, Madison K Rickabaugh, Paul Keselman, Munish Chauhan, Pamela V Tran, William M Brooks, Kenneth J Fischer, Andras Czirok, Irfan Saadi
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Abstract

Development of the embryonic palate requires that the palatal shelves (PS), which extend from maxillary processes, to grow bilaterally and vertically alongside the tongue. This growth continues until embryonic day (E) 13.5, after which the PS elevate above the tongue and adhere, completing the process by E14.5. Current models indicate that this elevation process involves a complex vertical-to-horizontal PS reorientation. While earlier studies have implied that reorientation occurs rapidly, the precise timing has not been resolved. Time-restricted pregnancies with a 1-h resolution showed that in 97% of C57BL/6J embryos, the PS were unelevated at E14.0. However, 6 h later, at E14.25, the PS had completed elevation in 80% of embryos, indicating that the PS elevate in a rapid and constrained timeframe. Interestingly, all E14.25 embryos with unelevated PS (20%) were female, suggesting sex differences in C57BL/6J PS elevation. In FVB/NJ embryos, the elevation window started earlier (E13.875-E14.25), and without any sex differences. An intermediate stage with unilateral PS elevation was frequently observed. Magnetic resonance imaging (MRI) of various stages showed that PS elevation began with posterior bilateral bulges, which then progressed laterally and anteriorly over time. During elevation, we observed increased cell proliferation in the PS lingual region. Within the bulge, cell orientation was tilted towards the tongue, and actomyosin activity was increased, which together may participate in horizontal projection of the bulge. Thus, our data reveal novel insights into rapid dynamic changes during PS elevation, and lay the foundation for future studies of normal and abnormal palatogenesis.

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对正常小鼠胚胎腭架升高动力学的新见解。
胚胎腭的发育需要从上颌突延伸出来的腭架(PS)沿舌两侧垂直生长。这种生长一直持续到胚胎期(E) 13.5,之后PS上升到舌头上方并粘附,在E14.5完成这一过程。目前的模型表明,这一抬升过程涉及一个复杂的垂直到水平的PS重新定位。虽然早期的研究表明,重新定位发生得很快,但精确的时间还没有得到解决。1小时分辨率的限时妊娠显示,97%的C57BL/6J胚胎在E14.0时PS未升高。然而,6小时后,在E14.25, 80%的胚胎的PS完成了升高,这表明PS在快速和有限的时间内升高。有趣的是,所有PS未升高的E14.25胚胎(20%)均为雌性,提示C57BL/6J PS升高存在性别差异。FVB/NJ胚胎的抬高窗开始时间较早(e13.875 ~ e14.25),且无性别差异。经常观察到单侧PS升高的中间阶段。不同阶段的磁共振成像(MRI)显示,PS升高始于双侧后部凸起,然后随着时间的推移向外侧和前方发展。在海拔升高期间,我们观察到PS舌区细胞增殖增加。在突起内,细胞向舌部倾斜,肌动球蛋白活性增加,这可能共同参与了突起的水平投射。因此,我们的数据揭示了PS升高过程中快速动态变化的新见解,并为未来正常和异常腭发生的研究奠定了基础。
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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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