Extracellular IL-37 promotes osteogenic and odontogenic differentiation of human dental pulp stem cells via autophagy

IF 3.5 3区 生物学 Q3 CELL BIOLOGY Experimental cell research Pub Date : 2021-10-01 Epub Date: 2021-08-16 DOI:10.1016/j.yexcr.2021.112780
Na Li , Ming Yan , Yan Chen , Yanqiu Wang , Jintao Wu , Lin Fu , Jinhua Yu
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引用次数: 6

Abstract

The osteogenic and odontogenic differentiation of dental pulp stem cells (DPSCs) contribute to restoration and regeneration of dental tissue. Previous study indicated that interleukin-37 (IL-37) was an anti-inflammatory factor that affected other pro-inflammatory signals. The aim of this study was to explore the effects of IL-37 on the differentiation of DPSCs. DPSCs were cultured in growth medium with different concentrations of IL-37. We selected the optimal concentration for the following experiments by alkaline phosphatase (ALP) activity analysis, quantitative reverse-transcription polymerase chain reaction (qRT-PCR) and Western blot. Cell counting kit assay (CCK-8) and 5-Ethynyl-2ʹ-Deoxyuridine (EdU) assay were conducted to assess the effects of IL-37 on the proliferation of DPSCs. ALP activity assay and staining, alizarin red S (ARS) staining, qRT‐PCR, Western blot as well as immunofluorescence staining were conducted to assess differentiation ability of DPSCs. Western blot, immunofluorescence staining and transmission electron microscopy (TEM) were utilized to examine cell autophagy. Results showed that IL-37 enhanced the osteogenic and odontogenic differentiation ability of DPSCs with no significant influence on the proliferation of DPSCs. Autophagy in DPSCs was activated by IL-37. Activation of autophagy enhanced osteogenesis and odontogenesis of DPSCs, whereas inhibition of autophagy suppressed DPSCs osteogenic and odontogenic differentiation. In conclusion, IL-37 increased osteogenic and odontogenic differentiation via autophagy.

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细胞外IL-37通过自噬促进人牙髓干细胞的成骨分化和成牙分化
牙髓干细胞(DPSCs)的成骨分化和牙源性分化有助于牙组织的修复和再生。先前的研究表明,白细胞介素-37 (IL-37)是一种影响其他促炎信号的抗炎因子。本研究旨在探讨IL-37对DPSCs分化的影响。在不同浓度IL-37的培养基中培养DPSCs。我们通过碱性磷酸酶(ALP)活性分析、定量反转录聚合酶链反应(qRT-PCR)和Western blot等方法选择最佳浓度进行后续实验。采用细胞计数试剂盒(CCK-8)和5-乙基-2′-脱氧尿苷(EdU)法检测IL-37对DPSCs增殖的影响。采用ALP活性测定和染色、茜素红S (ARS)染色、qRT - PCR、Western blot和免疫荧光染色等方法评价DPSCs的分化能力。采用Western blot、免疫荧光染色和透射电镜(TEM)检测细胞自噬。结果显示,IL-37增强了DPSCs的成骨和成牙分化能力,但对DPSCs的增殖无显著影响。IL-37可激活DPSCs的自噬。自噬激活促进了DPSCs的成骨和成牙,而自噬抑制了DPSCs的成骨和成牙分化。总之,IL-37通过自噬促进成骨分化和成牙分化。
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来源期刊
Experimental cell research
Experimental cell research 医学-细胞生物学
CiteScore
7.20
自引率
0.00%
发文量
295
审稿时长
30 days
期刊介绍: Our scope includes but is not limited to areas such as: Chromosome biology; Chromatin and epigenetics; DNA repair; Gene regulation; Nuclear import-export; RNA processing; Non-coding RNAs; Organelle biology; The cytoskeleton; Intracellular trafficking; Cell-cell and cell-matrix interactions; Cell motility and migration; Cell proliferation; Cellular differentiation; Signal transduction; Programmed cell death.
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