Hispidulin对牙髓干细胞成骨/成牙和内皮分化的影响。

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL Pharmaceuticals Pub Date : 2024-12-23 DOI:10.3390/ph17121740
Yeon Kim, Hyun-Joo Park, Mi-Kyoung Kim, Hyung Joon Kim, Yong-Il Kim, Soo-Kyung Bae, Moon-Kyoung Bae
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引用次数: 0

摘要

背景:人牙髓干细胞(Human dental pulp stem cells, HDPSCs)具有多系分化潜能和迁移能力,是实现基于HDPSCs的骨和牙再生所必需的。Hispidulin是一种天然存在的类黄酮,具有多种药理活性,但其对hdpsc生物学特性的影响尚不清楚。因此,我们研究了hispidulin对hdpsc分化潜能和迁移能力的影响,并阐明了其潜在机制。方法:采用碱性磷酸酶(ALP)和茜素红S (ARS)染色评价hdpsc的成骨/成牙能力。利用抓伤实验评估hdpsc的迁移能力。此外,通过毛细管发芽试验和评估CD31表达来检测HDPSCs的内皮分化。结果:Hispidulin显著增强了hdpsc的成骨/成牙分化,并增加了成骨/成牙分化标志物的表达。Hispidulin通过上调C-X-C趋化因子受体4型(CXCR4)介导HDPSCs的迁移。用hispidulin处理HDPSCs可以增强HDPSCs向内皮细胞的分化,这可以通过毛细血管发芽和内皮标志物表达的增加来证明。此外,我们证明了hispidulin激活ERK1/2信号,U0126对其的抑制作用显著抑制了hispidulin诱导的HDPSCs内皮分化。结论:本研究结果表明,hispidulin可有效促进hdpsc的成骨/牙源性和内皮分化以及迁移。这些结果表明hispidulin在牙髓再生和组织工程方面具有潜在的治疗应用价值。
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Effects of Hispidulin on the Osteo/Odontogenic and Endothelial Differentiation of Dental Pulp Stem Cells.

Background: Human dental pulp stem cells (HDPSCs) with multi-lineage differentiation potential and migration ability are required for HDPSC-based bone and dental regeneration. Hispidulin is a naturally occurring flavonoid with diverse pharmacological activities, but its effects on biological properties of HDPSCs remain unknown. Therefore, we investigated the effects of hispidulin on the differentiation potential and migration ability of HDPSCs and elucidated their underlying mechanisms. Methods: The osteo/odontogenic capacity of HDPSCs was assessed using the alkaline phosphatase (ALP) and Alizarin Red S (ARS) staining. The migration ability of HDPSCs was evaluated using a scratch wound assay. Furthermore, the endothelial differentiation of HDPSCs was examined by using a capillary sprouting assay and by assessing CD31 expression. Results: Hispidulin significantly enhanced the osteo/odontogenic differentiation of HDPSCs with increased expression of osteo/odontogenic differentiation markers. Hispidulin increased the migration of HDPSCs, which was mediated by the upregulation of C-X-C chemokine receptor type 4 (CXCR4). The treatment of HDPSCs with hispidulin enhanced the differentiation of HDPSCs into endothelial cells, as evidenced by increased capillary sprouting and endothelial marker expression. In addition, we demonstrated that hispidulin activated the ERK1/2 signaling, and its inhibition by U0126 significantly suppressed the hispidulin-induced endothelial differentiation of HDPSCs. Conclusions: These findings demonstrate that hispidulin effectively promotes the osteo/odontogenic and endothelial differentiation, and migration of HDPSCs. These results suggest that hispidulin may have potential therapeutic applications in dental pulp regeneration and tissue engineering.

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来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
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