番红花苷
牙周膜干细胞
Wnt信号通路
化学
丹麦克朗
牙周纤维
体内
运行x2
骨形态发生蛋白2
细胞生物学
药理学
碱性磷酸酶
生物化学
信号转导
体外
牙科
生物
医学
成骨细胞
生物技术
酶
出处
期刊:Oral Diseases
[Wiley]
日期:2023-02-13
卷期号:30 (3): 1429-1438
被引量:2
摘要
Abstract Objectives Crocin is a major class of medicinal components in saffron. This study aimed to determine whether crocin directly promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells (PDLSCs) in vitro and in vivo. Materials and Methods CCK8 cell proliferation assay, reverse transcription quantitative polymerase chain reaction (RT–qPCR), Western blot analysis and Alizarin Red staining were performed in PDLSCs using crocin as a stimulant. DKK1 was used to selectively inhibit Wnt/β‐catenin signaling, and Western blotting was performed to investigate the underlying mechanism. The PDLSCs were mixed with calcium phosphate cement and implanted into nude mice subcutaneously to study the effect of crocin on PDLSC osteogenic differentiation in vivo. Results The CCK‐8 assay showed that crocin did not promote the proliferation of PDLSCs. Treatment with 400 μM crocin significantly promoted PDLSC mRNA levels of ALP , COL1 and OCN ; RUNX2 and BMP2 protein expression; mineralized nodule formation in vitro and in vivo; and ALP activity in tissues in vivo. In addition, crocin significantly promoted the phosphorylation of β‐catenin and cyclin D1. DKK1 inhibits Wnt/β‐catenin activation and partially reverses crocin‐mediated promotion of PDLSC osteogenic differentiation. Conclusion Crocin may contribute to the regeneration of periodontal bone tissue.
科研通智能强力驱动
Strongly Powered by AbleSci AI