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柠檬酸对根尖乳头干细胞矿化和血管内皮生长因子分泌的影响。

The effect of citric acid on mineralisation and vascular endothelial growth factor secretion from apical papilla stem cells.

机构信息

Department of Pediatric Dentistry, Faculty of Dental Medicine, Medical University of Sofia, Sofia, Bulgaria.

Department of Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria.

出版信息

Acta Odontol Scand. 2024 Oct 1;83:546-552. doi: 10.2340/aos.v83.42026.

Abstract

OBJECTIVE

To investigate the influence of citric acid on the osteogenic and angiogenic potential of stem cells from apical papillae (SCAPs).

MATERIALS AND METHODS

Stem cells from apical papillae were isolated from freshly extracted third permanent molars. These cells were treated with 20 and 100 μM citric acid. Alizarin red staining was used to evaluate mineral deposition. The secreted levels of vascular endothelial growth factor (VEGF) were assessed by ELISA on days 18, 24 and 28. Immunofluorescence analysis was performed to assess the expression of surface markers after exposure to 20 and 100 μM citric acid.

RESULTS

Different mineralisation patterns were observed. Supplemented with citric acid, media showed more diffuse and less dense crystals. On day 18, most VEGF was secreted from the cells with no added citric acid. On day 24, there was a significant increase (p < 0.05) in the levels of VEGF secreted from cells treated with 20 μM citric acid. On day 28, cells from the control group did not secrete VEGF. There was a reduction in the levels of VEGF secreted by cells treated with 20 μM citric acid and a significant increase in the cells exposed to 100 μM citric acid (p < 0.05).

CONCLUSION

Citric acid can promote the differentiation of SCAPs and angiogenesis.

摘要

目的

研究柠檬酸对根尖乳头干细胞(SCAP)成骨和成血管潜能的影响。

材料和方法

从新鲜拔出的第三磨牙中分离出根尖乳头干细胞。用 20μM 和 100μM 的柠檬酸处理这些细胞。茜素红染色用于评估矿化沉积。通过 ELISA 在第 18、24 和 28 天评估血管内皮生长因子(VEGF)的分泌水平。免疫荧光分析用于评估暴露于 20μM 和 100μM 柠檬酸后表面标志物的表达。

结果

观察到不同的矿化模式。添加柠檬酸的培养基显示出更弥散、更稀疏的晶体。在第 18 天,没有添加柠檬酸的细胞分泌了大部分的 VEGF。在第 24 天,用 20μM 柠檬酸处理的细胞分泌的 VEGF 水平显著增加(p<0.05)。在第 28 天,对照组细胞未分泌 VEGF。用 20μM 柠檬酸处理的细胞分泌的 VEGF 水平降低,而暴露于 100μM 柠檬酸的细胞 VEGF 水平显著增加(p<0.05)。

结论

柠檬酸可以促进 SCAP 的分化和血管生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3388/11457356/dd3530c13231/AOS-83-42026-g001.jpg

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