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小鼠和人类之间进化保守的信号网络是额顶颅骨不同骨骨骼潜能的基础。

An Evolutionary Conserved Signaling Network Between Mouse and Human Underlies the Differential Osteoskeletal Potential of Frontal and Parietal Calvarial Bones.

作者信息

Menon Siddharth, Huber Julika, Duldulao Chris, Longaker Michael T, Quarto Natalina

机构信息

Hagey Laboratory for Pediatric Regenerative Medicine, Department of Surgery, School of Medicine, Stanford University, Stanford, CA, United States.

Division of Plastic and Reconstructive Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, United States.

出版信息

Front Physiol. 2021 Oct 21;12:747091. doi: 10.3389/fphys.2021.747091. eCollection 2021.

Abstract

The mammalian calvarial vault is an ancient and highly conserved structure among species, however, the mechanisms governing osteogenesis of the calvarial vault and how they might be conserved across mammalian species remain unclear. The aim of this study was to determine if regional differences in osteogenic potential of the calvarial vault, first described in mice, extend to humans. We derived human frontal and parietal osteoblasts from fetal calvarial tissue, demonstrating enhanced osteogenic potential both and of human frontal derived osteoblasts compared to parietal derived osteoblasts. Furthermore, we found shared differential signaling patterns in the canonical WNT, TGF-β, BMP, and FGF pathways previously described in the mouse to govern these regional differences in osteogenic potential. Taken together, our findings unveil evolutionary conserved similarities both at functional and molecular level between the mouse and human calvarial bones, providing further support that studies employing mouse models, are suitable for translational studies to human.

摘要

哺乳动物的颅顶是物种间古老且高度保守的结构,然而,调控颅顶骨生成的机制以及它们在哺乳动物物种间如何保守仍不清楚。本研究的目的是确定最初在小鼠中描述的颅顶骨成骨潜能的区域差异是否也存在于人类中。我们从胎儿颅骨组织中分离出人类额骨和顶骨成骨细胞,结果表明,与顶骨来源的成骨细胞相比,人类额骨来源的成骨细胞在增殖和分化方面均具有更强的成骨潜能。此外,我们发现,在小鼠中先前描述的经典WNT、TGF-β、BMP和FGF信号通路中存在共同的差异信号模式,这些信号通路调控了成骨潜能的区域差异。综上所述,我们的研究结果揭示了小鼠和人类颅骨在功能和分子水平上的进化保守相似性,进一步支持了使用小鼠模型的研究适用于向人类转化的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ba/8567095/82baf719a668/fphys-12-747091-g001.jpg

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