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阻断 LGR4 抑制根尖乳头干细胞的增殖和牙/骨向分化。

Blockade of LGR4 inhibits proliferation and odonto/osteogenic differentiation of stem cells from apical papillae.

机构信息

Jiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 136 Hanzhong Road, Nanjing, Jiangsu, 210029, China.

Department of Oral and Maxillofacial Surgery, Xuzhou Stomatological Hospital, Xuzhou, China.

出版信息

J Mol Histol. 2017 Dec;48(5-6):389-401. doi: 10.1007/s10735-017-9737-0. Epub 2017 Oct 6.

Abstract

During tooth root development, stem cells from apical papillae (SCAPs) are indispensable, and their abilities of proliferation, migration and odontoblast differentiation are linked to root formation. Leucine-rich repeat-containing GPCR 4 (LGR4) modulates the biological processes of proliferation and differentiation in multiple stem cells. In this study, we showed that LGR4 is expressed in all odontoblast cell lineage cells and Hertwig's epithelial root sheath (HERS) during the mouse root formation in vivo. In vitro we determined that LGR4 is involved in the Wnt/β-catenin signaling pathway regulating proliferation and odonto/osteogenic differentiation of SCAPs. Quantitative reverse-transcription PCR (qRT-PCR) confirmed that LGR4 is expressed during odontogenic differentiation of SCAPs. CCK8 assays and in vitro scratch tests, together with cell cycle flow cytometric analysis, demonstrated that downregulation of LGR4 inhibited SCAPs proliferation, delayed migration and arrested cell cycle progression at the S and G2/M phases. ALP staining revealed that blockade of LGR4 decreased ALP activity. QRT-PCR and Western blot analysis demonstrated that LGR4 silencing reduced the expression of odonto/osteogenic markers (RUNX2, OSX, OPN, OCN and DSPP). Further Western blot and immunofluorescence studies clarified that inhibition of LGR4 disrupted β-catenin stabilization. Taken together, downregulation of LGR4 gene expression inhibited SCAPs proliferation, migration and odonto/osteogenic differentiation by blocking the Wnt/β-catenin signaling pathway. These results indicate that LGR4 might play a vital role in SCAPs proliferation and odontoblastic differentiation.

摘要

在牙根发育过程中,根尖乳头干细胞(SCAP)是不可或缺的,其增殖、迁移和成牙本质分化能力与牙根形成有关。富含亮氨酸重复序列的 G 蛋白偶联受体 4(LGR4)调节多种干细胞的增殖和分化的生物学过程。在本研究中,我们表明 LGR4 在体内小鼠牙根形成过程中表达于所有成牙本质细胞谱系细胞和 Hertwig 上皮根鞘(HERS)中。在体外,我们确定 LGR4 参与调节 SCAP 的增殖和牙/成骨分化的 Wnt/β-catenin 信号通路。定量逆转录 PCR(qRT-PCR)证实 LGR4 在 SCAP 的牙源性分化过程中表达。CCK8 测定和体外划痕试验以及细胞周期流式细胞术分析表明,下调 LGR4 抑制 SCAP 增殖,延迟迁移并使细胞周期停滞在 S 和 G2/M 期。ALP 染色显示 LGR4 阻断降低了 ALP 活性。qRT-PCR 和 Western blot 分析表明,LGR4 沉默降低了牙/成骨标志物(RUNX2、OSX、OPN、OCN 和 DSPP)的表达。进一步的 Western blot 和免疫荧光研究阐明了抑制 LGR4 破坏了 β-catenin 的稳定。综上所述,下调 LGR4 基因表达通过阻断 Wnt/β-catenin 信号通路抑制 SCAP 的增殖、迁移和牙/成骨分化。这些结果表明 LGR4 可能在 SCAP 的增殖和牙本质分化中发挥重要作用。

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