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长链非编码 RNA LEF1-AS1 通过海绵吸附 miR-24-3p 促进牙髓干细胞的成骨分化。

LncRNA LEF1-AS1 promotes osteogenic differentiation of dental pulp stem cells via sponging miR-24-3p.

机构信息

Stomatological Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.

The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510080, Guangdong, China.

出版信息

Mol Cell Biochem. 2020 Dec;475(1-2):161-169. doi: 10.1007/s11010-020-03868-7. Epub 2020 Aug 11.

Abstract

The role of lncRNA LEF1-AS1 in the regulation of osteogenic differentiation of dental pulp stem cells (DPSCs) is still obscure. Here, we demonstrated that LncRNA LEF1-AS1 expression was associated with osteogenic differentiation of DPSCs and overexpression of LEF1-AS1 promoted osteogenic differentiation. Moreover, lncRNA LEF1-AS1 and miR-24-3p could directly regulate each other and LEF1-AS1 acted as sponge partner of miR-24-3p. Furthermore, LEF1-AS1 and miR-24-3p synergized to regulate osteogenic differentiation of DPSCs. Finally, we verified TGFBR1 was the direct target of miR-24-3p in osteogenic differentiation of DPSCs and miR-24-3p/LEF1-AS1 sponged to regulate TGFBR1 expression. Our study revealed a novel mechanism about how did lncRNA LEF1-AS1 execute function in osteogenesis of DPSCs and thus might serve as potential therapeutic target for the bone regeneration in the dental pulp.

摘要

长链非编码 RNA LEF1-AS1 在牙髓干细胞(DPSCs)成骨分化中的调节作用尚不清楚。在这里,我们证明了 LncRNA LEF1-AS1 的表达与 DPSCs 的成骨分化有关,过表达 LEF1-AS1 促进成骨分化。此外,lncRNA LEF1-AS1 和 miR-24-3p 可以直接相互调节,并且 LEF1-AS1 作为 miR-24-3p 的海绵体伙伴。此外,LEF1-AS1 和 miR-24-3p 协同调节 DPSCs 的成骨分化。最后,我们验证了 TGFBR1 是 miR-24-3p 在 DPSCs 成骨分化中的直接靶标,并且 miR-24-3p/LEF1-AS1 共同调节 TGFBR1 的表达。我们的研究揭示了长链非编码 RNA LEF1-AS1 在 DPSCs 成骨中发挥作用的新机制,因此可能成为牙髓再生中潜在的治疗靶点。

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