胰岛素样生长因子结合蛋白 5 促进牙髓干细胞的细胞增殖和成骨潜能取决于其核定位序列

IF 3.1 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Ziyan Sun, Jing Li, Huina Liu, Zhipeng Fan
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引用次数: 0

摘要

目的:牙髓干细胞(DPSCs)因其显著的功能被广泛用于组织再生。胰岛素样生长因子结合蛋白5(IGFBP5)可调控间充质干细胞(MSCs)的成骨分化,但其潜在的调控机制还需进一步研究:羧基荧光素琥珀酰亚胺酯、碱性磷酸酶(ALP)活性测定和茜素红染色用于揭示IGFBP5在DPSCs中的作用。蛋白表达水平用 Western 印迹法测定。免疫荧光用于观察细胞亚定位。通过裸鼠皮下移植观察 DPSCs 在体内的成骨过程:结果:IGFBP5增强了DPSCs的增殖和成骨分化。结果:IGFBP5能促进DPSCs的增殖和成骨分化。缺失IGFBP5的核定位序列(NLS)能阻止其核输入,并消除其对DPSCs的所有促进作用;伊维菌素刺激能减弱IGBFP5对ALP活性的增强作用。删除 NLS 后,IGFBP5 在体内促进骨样组织形成的作用消失。抑制IGFBP5核输入可减轻IGFBP5诱导的DPSCs中JNK(p-JNK)和磷酸化ERK(p-ERK)的磷酸化:我们的研究结果表明,IGFBP5 对 DPSCs 产生的细胞增殖和成骨分化效应与其进入细胞核密切相关,从而为组织再生提供了一个新的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Insulin-Like Growth Factor-Binding Protein 5 Promotes the Cell Proliferation and Osteogenic Potential of Dental Pulp Stem Cells Dependent on Its Nuclear Localisation Sequence.

Objectives: Dental pulp stem cells (DPSCs) have been extensively used for tissue regeneration owing to their notable capabilities. Insulin-like growth factor-binding protein 5 (IGFBP5) regulates osteogenic differentiation of mesenchymal stem cells (MSCs); however, the underlying regulatory mechanisms require further investigation.

Materials and methods: Carboxyfluorescein succinimidyl ester, an alkaline phosphatase (ALP) activity assay and Alizarin Red staining were used to reveal the role of IGFBP5 in DPSCs. Protein expression levels were determined using western blotting. Immunofluorescence was used to observe cell sub-localisation. Subcutaneous transplantation in nude mice was used to observe the osteogenesis of DPSCs in vivo.

Results: IGFBP5 enhanced the proliferation and osteogenic differentiation of DPSCs. Deletion of the nuclear localisation sequence (NLS) of IGFBP5 prevented its nuclear import and abolished all its promoting effects on DPSCs; ivermectin stimulation attenuated the enhancement of ALP activity by IGBFP5. Bone-like tissue formation promoted by IGFBP5 in vivo vanishes when the NLS is deleted. Inhibition of IGFBP5 nuclear import attenuated the IGFBP5-induced phosphorylation of JNK (p-JNK) and phosphorylated ERK (p-ERK) in DPSCs.

Conclusion: Our findings suggest that cell proliferation and osteogenic differentiation effects exerted by IGFBP5 on DPSCs are closely associated with their entry into the nucleus, thereby providing a novel potential target for tissue regeneration.

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来源期刊
Journal of oral rehabilitation
Journal of oral rehabilitation 医学-牙科与口腔外科
CiteScore
5.60
自引率
10.30%
发文量
116
审稿时长
4-8 weeks
期刊介绍: Journal of Oral Rehabilitation aims to be the most prestigious journal of dental research within all aspects of oral rehabilitation and applied oral physiology. It covers all diagnostic and clinical management aspects necessary to re-establish a subjective and objective harmonious oral function. Oral rehabilitation may become necessary as a result of developmental or acquired disturbances in the orofacial region, orofacial traumas, or a variety of dental and oral diseases (primarily dental caries and periodontal diseases) and orofacial pain conditions. As such, oral rehabilitation in the twenty-first century is a matter of skilful diagnosis and minimal, appropriate intervention, the nature of which is intimately linked to a profound knowledge of oral physiology, oral biology, and dental and oral pathology. The scientific content of the journal therefore strives to reflect the best of evidence-based clinical dentistry. Modern clinical management should be based on solid scientific evidence gathered about diagnostic procedures and the properties and efficacy of the chosen intervention (e.g. material science, biological, toxicological, pharmacological or psychological aspects). The content of the journal also reflects documentation of the possible side-effects of rehabilitation, and includes prognostic perspectives of the treatment modalities chosen.
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