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间歇性压缩力通过Yes相关蛋白调节人牙周膜细胞行为。

Intermittent compressive force regulates human periodontal ligament cell behavior via yes-associated protein.

作者信息

Klincumhom Nuttha, Lorthongpanich Chanchao, Thumanu Kanjana, Septham Praphasri, Phomyu Wutthikiat, Issaragrisil Surapol, Pavasant Prasit

机构信息

Center of Excellence for Regenerative Dentistry and Department of Anatomy, Faculty of Dentistry, Chulalongkorn University, Bangkok 10330, Thailand.

Siriraj Center of Excellence for Stem Cell Research, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.

出版信息

Heliyon. 2022 Oct 1;8(10):e10845. doi: 10.1016/j.heliyon.2022.e10845. eCollection 2022 Oct.

Abstract

Intermittent compressive force influences human periodontal ligament (PDL) cell behavior that facilitates periodontal tissue regeneration. In response to mechanical stimuli, Yes-associated protein (YAP) has been recognized as a mechanosensitive transcriptional activator that regulates cell proliferation and cell fate decisions. This study aimed to investigate whether compressive forces influence cell proliferation and cell fate decisions of human PDL cells via YAP signaling. YAP expression was silenced by shRNA. The effect of YAP on cell proliferation, adipogenesis and osteogenesis of PDL cells under ICF loading were determined. Adipogenic differentiation bias upon ICF loading was confirmed by fourier-transform infrared spectroscopy (FTIR). The results revealed that ICF-induced YAP promotes osteogenesis, but it inhibits adipogenesis in PDL cells. Depletion of YAP results in PDL cells that are irresponsive to ICF and, therefore, the failure of the PDL cells to undergo osteogenic differentiation. This was shown by a significant reduction in calcium deposited in the CF-derived osteoblasts of the YAP-knockdown (YAP-KD) PDL cells. As to control treatment, reduction of YAP promoted adipogenesis, whereas ICF-induced YAP inhibited this mechanism. However, the adipocyte differentiation in YAP-KD cells was not affected upon ICF treatment as the YAP-KD cells still exhibited a better adipogenic differentiation that was unrelated to the ICF. This study demonstrated that, in response to ICF treatment, YAP could be a crucial mechanosensitive transcriptional activator for the regulation of PDL cell behavior through a mechanobiological process. Our results may provide the possibility of facilitating PDL tissue regeneration by manipulation of the Hippo-YAP signaling pathway.

摘要

间歇性压缩力影响人类牙周膜(PDL)细胞行为,促进牙周组织再生。响应机械刺激,Yes相关蛋白(YAP)已被认为是一种机械敏感的转录激活因子,可调节细胞增殖和细胞命运决定。本研究旨在探讨压缩力是否通过YAP信号通路影响人PDL细胞的增殖和细胞命运决定。YAP表达通过shRNA沉默。测定了YAP对ICF加载下PDL细胞增殖、脂肪生成和成骨的影响。通过傅里叶变换红外光谱(FTIR)证实了ICF加载后脂肪生成分化偏向。结果显示,ICF诱导的YAP促进成骨,但抑制PDL细胞中的脂肪生成。YAP的缺失导致PDL细胞对ICF无反应,因此PDL细胞无法进行成骨分化。这表现为YAP敲低(YAP-KD)PDL细胞的CF衍生成骨细胞中钙沉积显著减少。对于对照处理,YAP的减少促进脂肪生成,而ICF诱导的YAP抑制该机制。然而,ICF处理对YAP-KD细胞中的脂肪细胞分化没有影响,因为YAP-KD细胞仍然表现出更好的脂肪生成分化,这与ICF无关。本研究表明,响应ICF处理,YAP可能是通过机械生物学过程调节PDL细胞行为的关键机械敏感转录激活因子。我们的结果可能为通过操纵Hippo-YAP信号通路促进PDL组织再生提供可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a406/9561743/8b76403f84bd/gr1.jpg

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