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[Preparation of nano BaTiO3@Au Schottky junction coatings on titanium implant and the influence on osteogenic properties of rat bone marrow stem cells]. 纳米BaTiO3@Au Schottky结膜在钛种植体上的制备及成骨性能评价
Q4 Medicine Pub Date : 2025-11-09 DOI: 10.3760/cma.j.cn112144-20250702-00242
X L Guo, D H Sun, L Y Li, L F Zhong, X Y Wang, Q Zhou, L Z Zhao
<p><p><b>Objective:</b> To prepare a nano-barium titanate@gold Schottky junction (nano-BaTiO<sub>3</sub>@Au) coating and investigate its effects on the adhesion, proliferation, and osteogenic differentiation of bone marrow stem cells (BMSCs), aiming to explore a titanium surface modification strategy with superior osteogenic activity. <b>Methods:</b> Pure titanium specimens served as the control group (Ti group). Titanium dioxide coatings were prepared on their surfaces via anodic oxidation. Nano-barium titanate (nBTO group) was further synthesized using the hydrothermal method. Gold nanoparticles were grown in situ on the nano-BaTiO<sub>3</sub> via high-temperature reduction of chloroauric acid using sodium citrate, yielding the nano-barium titanate@gold Schottky junction coating (nBTO@Au group). Surface morphology was observed by scanning electron microscopy (SEM). Elemental composition was analyzed using X-ray energy dispersive spectrum (EDS) and X-ray photoelectron spectroscopy (XPS). Crystal structure was analyzed using X-ray diffraction (XRD) and Raman spectroscopy. Hydrophilicity was assessed via water contact angle measurement. Specimens were co-cultured with BMSCs to evaluate biocompatibility and osteogenic properties. Cell proliferation on days 1, 3, 5, and 7 was assessed using the cell counting kit-8 (CCK-8) assay. Cytotoxicity towards BMSCs was assessed using live/dead cell staining. Cell morphology and adhesion were observed using cytoskeleton staining. Alkaline phosphatase (ALP) expression in BMSCs after 7 days was quantified using an ALP activity assay and ALP staining. Extracellular matrix mineralization after 7 days was evaluated using alizarin red staining and quantification assay. Each experiment was performed using three specimens per group. <b>Results:</b> Scanning electron microscopy revealed that gold nanoparticles with the diameter of(14.838±0.718) nm, uniform in size and homogeneously distributed, were successfully grown in situ on the surface of the nBTO coating. EDS and XPS confirmed the presence of Ba, Ti, O, and Au elements in the nBTO@Au composite coating. XRD and Raman spectroscopy analysis indicated that the nanostructured barium titanate (nBTO) coating was synthesized via a hydrothermal method.Water contact angle measurements showed that the contact angle was 66.8°± 0.45° for the control group, 22.55°±0.42° for the nBTO group, and 26.78°±1.15° for the nBTO@Au group, indicating good hydrophilicity of both nBTO and nBTO@Au coatings. On day 1 and day 3 of culture, the cell proliferation in the nBTO group was significantly lower than that in the control group (<i>P</i><0.05). In contrast, no significant differences were observed between the nBTO@Au group and either the control group or the nBTO group (all <i>P</i>>0.05). By day 5, the cell proliferation of nBTO@Au groups was significantly lower than that of the control group (<i>P</i><0.05), and the cell proliferation of nBTO group was significantly lower than that of
目的:制备纳米钡titanate@gold Schottky结(nano-BaTiO3@Au)涂层,研究其对骨髓干细胞(BMSCs)粘附、增殖和成骨分化的影响,探索具有优异成骨活性的钛表面修饰策略。方法:以纯钛标本为对照组(钛组)。通过阳极氧化在其表面制备了二氧化钛涂层。采用水热法进一步合成纳米钛酸钡(nBTO基团)。利用柠檬酸钠高温还原氯金酸,在纳米batio3上原位生长金纳米粒子,得到纳米钡titanate@gold肖特基结涂层(nBTO@Au基团)。用扫描电镜(SEM)观察表面形貌。采用x射线能谱(EDS)和x射线光电子能谱(XPS)分析元素组成。利用x射线衍射(XRD)和拉曼光谱分析了晶体结构。通过水接触角测定亲水性。将标本与骨髓间充质干细胞共培养,评价其生物相容性和成骨性能。使用细胞计数试剂盒-8 (CCK-8)测定第1、3、5和7天的细胞增殖情况。使用活/死细胞染色评估对骨髓间充质干细胞的细胞毒性。细胞骨架染色观察细胞形态和粘附情况。采用碱性磷酸酶(ALP)活性测定和ALP染色法测定7天后骨髓间充质干细胞中碱性磷酸酶(ALP)的表达。7 d后用茜素红染色和定量分析评价细胞外基质矿化。每组取3只标本。结果:扫描电镜显示,在nBTO涂层表面原位成功生长出平均直径约15.36 nm的金纳米颗粒,粒径均匀,分布均匀。EDS和XPS证实了nBTO@Au复合涂层中存在Ba、Ti、O和Au元素。XRD和拉曼光谱分析表明,采用水热法制备了纳米钛酸钡(nBTO)涂层。水接触角测量结果表明,对照组的接触角为66.8°±0.45°,nBTO组的接触角为22.55°±0.42°,nBTO@Au组的接触角为26.78°±1.15°,表明nBTO和nBTO@Au涂层均具有良好的亲水性。在培养第1天和第3天,nBTO组细胞增殖显著低于对照组(P0.05)。相比之下,nBTO@Au组与对照组或nBTO组之间均无显著差异(P < 0.05)。第5天,nBTO@Au组细胞增殖能力显著低于对照组(P0.05), nBTO组细胞增殖能力显著低于对照组和nBTO@Au组(P0.05)。第7天,各组细胞增殖能力比较,差异均无统计学意义(F=1.62, P < 0.05)。活/死细胞染色结果显示,各组细胞存活率均超过90%,形态正常,死亡细胞少,表明nBTO@Au涂层具有良好的生物相容性。与对照组相比,nBTO组和nBTO@Au组均促进了细胞的粘附和扩散,但两组间细胞形态无显著差异。ALP染色显示nBTO@Au组染色面积更大,颜色更深。定量结果显示nBTO@Au组ALP活性显著高于nBTO组和对照组(P0.05), nBTO组ALP活性也显著高于对照组(P0.05)。茜素红染色显示nBTO@Au组颜色最深,nBTO组次之,对照组颜色最浅。定量分析进一步证实nBTO@Au组钙结节沉积量显著大于其他两组(P0.05), nBTO组钙结节沉积量也显著大于对照组(P0.05)。结论:本研究成功制备了具有良好生物相容性和增强成骨性能的nBTO@Au涂层。
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引用次数: 0
[Advances in diagnostic criteria and multimodal diagnostic techniques for endodontics]. 【牙髓学诊断标准及多模态诊断技术进展】。
Q4 Medicine Pub Date : 2025-11-09 DOI: 10.3760/cma.j.cn112144-20250402-00117
J X Xiao, S Mai

Pulpitis is an inflammatory response of the pulp tissue triggered by bacterial infection or mechanical trauma. Current diagnostic criteria classify it into two categories: reversible pulpitis and irreversible pulpitis. Wolters et al. proposed a four-level classification of pulpitis based on clinical symptoms, establishing a guiding framework for minimally invasive endodontics. With the development of precision medicine and molecular biological diagnostic techniques, biomarker detection has emerged as a quantitative tool for determining endodontic status. Diagnostic techniques that integrate multimodal information such as pain intensity assessment, endodontic diagnostic testing and biomarker detection can break through the limitations of traditional or single diagnostic methods, which not only providing clinicians with more scientific and comprehensive ideas for endodontic status assessment and treatment decision options, but also promoting the transition to precision medicine for endodontic diagnosis.

牙髓炎是由细菌感染或机械创伤引起的牙髓组织炎症反应。目前的诊断标准分为两类:可逆性牙髓炎和不可逆性牙髓炎。Wolters等人根据临床症状提出了牙髓炎的四级分类,建立了微创牙髓学的指导框架。随着精准医学和分子生物学诊断技术的发展,生物标志物检测已成为确定牙髓状态的定量工具。整合疼痛强度评估、牙髓诊断检测、生物标志物检测等多模式信息的诊断技术,可以突破传统或单一诊断方法的局限,不仅为临床医生提供更科学、全面的牙髓状态评估和治疗决策选择思路,还可以促进牙髓诊断向精准医学过渡。
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引用次数: 0
[Neural regulation mechanism in bone regeneration]. 骨再生的神经调节机制。
Q4 Medicine Pub Date : 2025-11-09 DOI: 10.3760/cma.j.cn112144-20250804-00298
Y M Song, X Y Li, L J Guo

The global aging population has intensified the incidence of degenerative bone diseases and the therapeutic demand for traumatic bone injuries, thereby making bone regenerative medicine a research focus. There is a close connection and interaction between the skeletal system and the nervous system, and innervation plays an indispensable regulatory role in the process of bone regeneration: the sympathetic nervous system exerts a negative regulatory effect during bone regeneration, while the parasympathetic nervous system plays a positive regulatory role in this process. Nerve fibers within bones are distributed alongside blood vessels, with their density decreasing from the periosteum to the cancellous bone. Nerve signals regulate bone regeneration either by directly acting on target cell receptors or indirectly modulating the metabolism of the local microenvironment (such as the levels of inflammatory factors and the supply of nutrients). A variety of neuropeptides (e.g., calcitonin gene-related peptide, substance P, neuropeptide Y, vasoactive intestinal peptide, etc.) play a crucial role in bone tissue, constructing a "neuro-osseous" regulatory axis, which in turn regulates the osteoblast-osteoclast balance, angiogenesis, and the homeostasis of the local microenvironment. This review focuses on the neural regulatory mechanisms in bone regeneration, with an emphasis on sorting out the functions of key neuropeptides and related neurotransmitters. Neuropeptides are the core mediators of neuro-osseous interaction; however, the interaction network among neuropeptides remains to be further clarified, which requires the application of advanced in vitro models such as three-dimensional bioprinted bone models and organoid technology, as well as cutting-edge techniques like single-cell sequencing for analysis. In the future, the integration of neural regulation strategies with traditional bone regeneration technologies, along with the expansion into interdisciplinary fields such as neuro-vascular and neuro-muscular fields, is expected to provide new directions for the treatment of bone defects and large maxillofacial tissue defects, and promote the transformation of regenerative medicine from prosthetic treatment to functional and neurotized tissue regeneration.

全球人口老龄化加剧了退行性骨病的发病率和外伤性骨损伤的治疗需求,骨再生医学成为研究热点。骨骼系统与神经系统有着密切的联系和相互作用,神经支配在骨再生过程中起着不可或缺的调节作用:交感神经系统在骨再生过程中起负向调节作用,副交感神经系统在骨再生过程中起正向调节作用。骨内神经纤维沿血管分布,其密度由骨膜向松质骨递减。神经信号通过直接作用于靶细胞受体或间接调节局部微环境的代谢(如炎症因子的水平和营养物质的供应)来调节骨再生。多种神经肽(如降钙素基因相关肽、P物质、神经肽Y、血管活性肠肽等)在骨组织中起着至关重要的作用,构建了“神经-骨”调节轴,进而调节成骨-破骨细胞平衡、血管生成和局部微环境的稳态。本文综述了骨再生的神经调控机制,重点梳理了关键神经肽和相关神经递质的功能。神经肽是神经-骨相互作用的核心介质;然而,神经肽之间的相互作用网络仍有待进一步阐明,这需要应用先进的体外模型,如三维生物打印骨模型和类器官技术,以及单细胞测序等尖端技术进行分析。未来,神经调节策略与传统骨再生技术的融合,以及向神经血管、神经肌肉等跨学科领域的拓展,有望为骨缺损和颌面大型组织缺损的治疗提供新的方向,推动再生医学从修复性治疗向功能化、神经化组织再生的转变。
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引用次数: 0
[Maternally inherited KCNQ1 mutation-related gingival fibromatosis: a case report and literature review]. 【母系遗传KCNQ1突变相关牙龈纤维瘤病1例报告及文献复习】。
Q4 Medicine Pub Date : 2025-11-09 DOI: 10.3760/cma.j.cn112144-20250605-00207
J L Xu, D Chen, X Y Guo, H Jia, Y L Zhang, X P Wang, S Q Wei, X H Duan
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引用次数: 0
[Application of pouch technique in the reconstruction of severe alveolar bone defects: a case report]. [应用眼袋技术修复严重牙槽骨缺损1例]。
Q4 Medicine Pub Date : 2025-11-09 Epub Date: 2025-11-03 DOI: 10.3760/cma.j.cn112144-20250917-00366
M H Wang, Y H Hu, D H Zou

Guided bone regeneration (GBR) has been widely used in the repair and reconstruction of alveolar bone defects. However, conventional GBR techniques often fail to achieve the desired bone augmentation for severe bone defects (diameter≥5 mm). To address this limitation, several innovative GBR-based approaches, such as the tenting and sausage techniques have been developed, achieving varying degrees of clinical success. Nonetheless, these methods still face considerable challenges, including secondary trauma from autogenous bone harvesting, high technical sensitivity, and limited scalability. In response, our team proposed a novel treatment concept centered on the principle of "stability-core", and developed a new therapeutic strategy that avoids the use of autogenous bone. This strategy involves the development of a new series of tent-peg medical devices and the introduction of the pouch technique, which has been successfully applied in clinical practice. This case report presents the successful use of the pouch technique for vertical ridge augmentation in the maxillary posterior region. At 8-month follow-up, substantial vertical bone gain and restoration of the alveolar ridge contour were achieved. Implant placement and prosthetic rehabilitation were completed with satisfactory functional recovery. The patient reported a positive treatment experience. This technique offers a promising and practical solution for alveolar bone reconstruction.

引导骨再生(GBR)在牙槽骨缺损的修复和重建中得到了广泛的应用。然而,对于严重骨缺损(直径≥5mm),传统的GBR技术往往无法实现所需的骨增强。为了解决这一限制,一些基于gbr的创新方法,如帐篷技术和香肠技术已经开发出来,取得了不同程度的临床成功。尽管如此,这些方法仍然面临着相当大的挑战,包括自体骨采集的二次创伤、高技术敏感性和有限的可扩展性。为此,我们的团队提出了一种以“稳定核心”为核心的新治疗理念,并开发了一种避免使用自体骨的新治疗策略。这一策略涉及开发一系列新的帐篷式医疗设备和引入育儿袋技术,该技术已成功应用于临床实践。本病例报告介绍了成功使用袋技术在上颌后区垂直隆起。在8个月的随访中,获得了大量的垂直骨增加和牙槽嵴轮廓的恢复。种植体植入和假肢康复均完成,功能恢复满意。病人报告了积极的治疗经历。该技术为牙槽骨重建提供了一种很有前途的实用方法。
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引用次数: 0
[Research status and development trends of dental pulpitis biomarkers]. [牙髓炎生物标志物研究现状及发展趋势]。
Q4 Medicine Pub Date : 2025-11-09 DOI: 10.3760/cma.j.cn112144-20250314-00082
H Y Liu, Y L Cai, X Wei

Pulpitis is an inflammatory response of dental pulp tissue triggered by external stimuli such as bacterial infection, mechanical trauma, and iatrogenic injury. Accurate diagnosis of pulpitis is essential for the success of minimally invasive endodontic treatments. However, the current diagnostic framework lacks objective indicators capable of precisely assessing the severity of pulp inflammation. Recent studies have revealed that biomarkers such as matrix metalloproteinases, cytokines, chemokines, non-coding RNAs, growth factors, and signaling molecules are closely associated with the degree of pulp inflammation. These findings suggested that biomarker-based molecular diagnostics held significant promise for advancing precision and minimally invasive approaches in endodontics. This review systematically discusses the current research progress, challenges, and future directions of biomarkers in the diagnosis and treatment of pulpitis.

牙髓炎是由细菌感染、机械创伤、医源性损伤等外界刺激引起的牙髓组织炎症反应。牙髓炎的准确诊断是微创根管治疗成功的关键。然而,目前的诊断框架缺乏能够精确评估牙髓炎症严重程度的客观指标。近年来的研究表明,基质金属蛋白酶、细胞因子、趋化因子、非编码rna、生长因子、信号分子等生物标志物与牙髓炎症程度密切相关。这些发现表明,基于生物标志物的分子诊断对于提高牙髓学的精度和微创方法具有重要的前景。本文就生物标志物在牙髓炎诊断和治疗中的研究进展、面临的挑战及未来发展方向进行了系统的综述。
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引用次数: 0
[Research progress in Runt-related transcription factor 2 regulation of bone remodeling and tooth eruption]. [runt相关转录因子2调控骨重塑和牙萌的研究进展]。
Q4 Medicine Pub Date : 2025-11-09 DOI: 10.3760/cma.j.cn112144-20250613-00220
Y Liu, D D Liu, X Y Sun, J Y Du, S G Zheng

Cleidocranial dysplasia, a rare genetic disorder primarily caused by Runt-related transcription factor 2 (RUNX2) heterozygous mutation, serves as a representative model for investigating regulatory mechanisms of RUNX2 in bone remodeling and tooth eruption. As a master transcription factor governing mineralized tissue development, RUNX2 orchestrates bone remodeling and tooth eruption through diverse regulatory networks. It drives alveolar bone formation via transcriptional activation, integration of multiple signaling cascades, and epigenetic modifications, thereby generating the biomechanical force for tooth eruption. Concurrently, RUNX2 promotes osteoblastic secretion of osteoclastogenic factors and directly regulates osteoclast precursor differentiation, facilitating bone resorption at the coronal aspect of dental follicles to estavlish the eruption pathway. Furthermore, RUNX2 modulates eruption progression by participating in stress-induced biological signal transduction within dental follicle cells (DFCs), remodeling the DFCs microenvironment, and regulating DFCs senescence. RUNX2 also influences root development via the NOTUM-Wnt axis, providing auxiliary biomechanical conditions conducive to eruption. This review systematically delineates the pivotal role of RUNX2 in coordinating bone remodeling and tooth eruption. Future studies should leverage organoid models and multi-omics technologies to further elucidate the spatiotemporal regulatory networks of RUNX2, potentially advancing precision diagnostics and therapeutics for rare skeletal-dental developmental disorders.

锁骨颅发育不良(CCD)是一种罕见的遗传性疾病,主要由runt相关转录因子2 (RUNX2)杂合突变引起,是研究RUNX2在骨重塑和牙齿萌出中的调控机制的代表性模型。作为控制矿化组织发育的主要转录因子,RUNX2通过多种调节网络协调骨重塑和牙齿萌出。它通过转录激活、多种信号级联的整合和表观遗传修饰来驱动牙槽骨的形成,从而产生出牙的生物力学力。同时,RUNX2促进成骨细胞分泌破骨因子,直接调控破骨细胞前体分化,促进牙囊冠状面骨吸收,建立出牙通路。此外,RUNX2通过参与牙滤泡细胞(dfc)内应力诱导的生物信号转导、重塑dfc微环境和调节dfc衰老来调节萌牙进程。RUNX2还通过NOTUM-Wnt轴影响根的发育,提供有利于爆发的辅助生物力学条件。本文系统地阐述了RUNX2在骨重塑和牙齿萌出中的关键作用。未来的研究应利用类器官模型和多组学技术进一步阐明RUNX2的时空调控网络,有可能推进罕见骨牙发育障碍的精确诊断和治疗。
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引用次数: 0
[Research on the negative regulation of osteoclast differentiation by hairy and enhancer of split related protein 2 through nuclear factor of activated T cells cytoplasmic 1]. 【毛状及分裂相关蛋白2增强子通过活化T细胞胞质1的核因子负向调控破骨细胞分化的研究】。
Q4 Medicine Pub Date : 2025-11-09 DOI: 10.3760/cma.j.cn112144-20250313-00078
Z X Qiao, Y Ban, L L Liu, L N Shao
<p><p><b>Objective:</b> To explore the effect of hairy and enhancer of split related protein 2 (Hey2) on osteoclast differentiation through the activation of nuclear factor of activated T cells cytoplasmic 1 (NFATc1). <b>Methods:</b> RAW264.7 cells were induced with receptor activator of NF-κB ligand (RANKL) to differentiate into osteoclasts. Experimental groups were divided by different concentrations of RANKL (0, 10, 20, 50 μg/L) and different processing time (0, 3, 5, 7 days). Hey2 overexpression experiment was grouped as follows: blank control group, RANKL group, empty plasmid vector control group (Hey2-NC+RANKL), Hey2 overexpression group (Hey2-OE+RANKL); similarly, groups in Hey2 knockdown experiment were as follows: blank control group, RANKL group, negative control group (si-NC+RANKL), Hey2 knockdown group (si-Hey2+RANKL). Chromatin immunoprecipitation experiment groups were divided as non-specific IgG control group (IgG control group), non-specific IgG group (IgG RANKL group), Hey2-specific antibody control group (anti-Hey2 control group), Hey2-specific antibody group (anti-Hey2-RANKL group). For the different RANKL concentration groups and different induction time groups, real-time fluorescent quantitative PCR (RT-qPCR) was used to detect the mRNA expressions of nuclear factor of NFATc1, cathepsin K (CTSK), and cellular feline osteosarcoma oncogene (c-Fos) and tartrate-resistant acid phosphatase (TRAP) staining was used to assess the formation of multinucleated osteoclasts. After Hey2 overexpression or knockdown, RT-qPCR and Western blotting were used to detect the gene and protein expressions of NFATc1, c-Fos, and CTSK. TRAP staining was used to evaluate the formation of multinucleated osteoclasts. Bioinformatics prediction (NCBI, JASPAR) and chromatin immunoprecipitation (ChIP) assay were used to validate the binding of Hey2 to the NFATc1 promoter region. <b>Results:</b> During the osteoclastic differentiation of RAW 264.7 cells induced by RANKL, the expression of Hey2 could be detected, and the expression level of Hey2 decreased with the increase of RANKL concentration and induction time. In the 50 μg/L RANKL group, the expression levels of Hey2 gene (0.18±0.00) and protein (0.22±0.02) were significantly lower than those in the control group (1.00±0.00, 0.52±0.01) (<i>t</i>=41.67, 12.88; both <i>P</i><0.001). In the 50 μg/L RANKL group inducted for 5 days, the expression levels of Hey2 gene (0.27±0.02) and protein (0.79±0.01) were significantly lower than those in the control group (1.00±0.00, 1.15±0.02) (<i>t</i>=11.47, 108.60; both <i>P</i><0.001). Hey2 overexpression significantly reduced the gene and protein expressions of NFATc1, c-Fos, and CTSK, as well as the production of TRAP-positive cells (all <i>P</i><0.05). Hey2 knockdown significantly increased the gene and protein expressions of NFATc1, c-Fos, and CTSK, as well as the production of TRAP-positive cells (all <i>P</i><0.05). After inducing RAW264.7 cells with 50 μg/L RANK
目的:探讨毛状分裂相关蛋白2 (hairy and enhancer of split related protein 2, Hey2)通过激活活化T细胞胞浆核因子1 (nuclear factor of activated T cells cytoplasmic 1, NFATc1)对破骨细胞分化的影响。方法:采用NF-κB配体受体激活剂(receptor activator of NF-κB ligand, RANKL)诱导RAW264.7细胞向破骨细胞分化。实验组按RANKL浓度(0、10、20、50 μg/L)和处理时间(0、3、5、7 d)分组。Hey2过表达实验分为:空白对照组、RANKL组、空质粒载体对照组(Hey2- nc +RANKL)、Hey2过表达组(Hey2- oe +RANKL);同样,Hey2敲低实验组分为空白对照组、RANKL组、阴性对照组(si-NC+RANKL)、Hey2敲低组(si-Hey2+RANKL)。染色质免疫沉淀实验组分为非特异性IgG对照组(IgG对照组)、非特异性IgG+RANKL组(IgG RANKL组)、hey2特异性抗体对照组(抗hey2对照组)、hey2特异性抗体+RANKL组(抗hey2 -RANKL组)。对于不同RANKL浓度组和不同诱导时间组,采用实时荧光定量PCR (RT-qPCR)检测活化T细胞核因子mRNA表达,细胞质1 (NFATc1)、组织蛋白酶K (CTSK)、细胞性猫骨肉瘤癌基因(c-Fos)和抗酒石酸酸性磷酸酶(TRAP)染色评估多核破骨细胞的形成。Hey2过表达或敲低后,采用RT-qPCR和Western blotting检测NFATc1、c-Fos、CTSK的基因和蛋白表达。TRAP染色观察多核破骨细胞的形成情况。采用生物信息学预测(NCBI, JASPAR)和染色质免疫沉淀(ChIP)试验验证Hey2与NFATc1启动子区域的结合。结果:RANKL诱导RAW 264.7细胞破骨分化过程中可检测到Hey2的表达,且随着RANKL浓度和诱导时间的增加,Hey2的表达水平降低。50 μg/L RANKL组Hey2基因表达量(0.18±0.00)和蛋白表达量(0.22±0.02)显著低于对照组(1.00±0.00、0.52±0.01)(t=41.67、12.88,p均为0.001)。50 μg/L RANKL诱导5 d后,Hey2基因表达量(0.27±0.02)和蛋白表达量(0.79±0.01)显著低于对照组(1.00±0.00、1.15±0.02)(t=11.47、108.60,p均为0.001)。Hey2过表达可显著降低NFATc1、c-Fos、CTSK基因和蛋白的表达,显著降低trap阳性细胞的产生(均P0.05)。敲低Hey2显著增加了NFATc1、c-Fos、CTSK基因和蛋白的表达以及trap阳性细胞的产生(均P0.05)。50 μg/L RANKL诱导RAW264.7细胞1 d后,ChIP结果显示,在Hey2抗体处理的2个样本组中,抗Hey2-RANKL组NFATc1启动子区(-400 ~ 200 bp)的检测水平(18.06±0.06)显著高于抗Hey2对照组(13.37±0.36)(t=12.56, P0.001)。结论:Hey2可与下游靶基因NFATc1在启动子400 ~ -200 bp区域结合。作为一种转录抑制因子,Hey2抑制破骨细胞的分化。
{"title":"[Research on the negative regulation of osteoclast differentiation by hairy and enhancer of split related protein 2 through nuclear factor of activated T cells cytoplasmic 1].","authors":"Z X Qiao, Y Ban, L L Liu, L N Shao","doi":"10.3760/cma.j.cn112144-20250313-00078","DOIUrl":"10.3760/cma.j.cn112144-20250313-00078","url":null,"abstract":"&lt;p&gt;&lt;p&gt;&lt;b&gt;Objective:&lt;/b&gt; To explore the effect of hairy and enhancer of split related protein 2 (Hey2) on osteoclast differentiation through the activation of nuclear factor of activated T cells cytoplasmic 1 (NFATc1). &lt;b&gt;Methods:&lt;/b&gt; RAW264.7 cells were induced with receptor activator of NF-κB ligand (RANKL) to differentiate into osteoclasts. Experimental groups were divided by different concentrations of RANKL (0, 10, 20, 50 μg/L) and different processing time (0, 3, 5, 7 days). Hey2 overexpression experiment was grouped as follows: blank control group, RANKL group, empty plasmid vector control group (Hey2-NC+RANKL), Hey2 overexpression group (Hey2-OE+RANKL); similarly, groups in Hey2 knockdown experiment were as follows: blank control group, RANKL group, negative control group (si-NC+RANKL), Hey2 knockdown group (si-Hey2+RANKL). Chromatin immunoprecipitation experiment groups were divided as non-specific IgG control group (IgG control group), non-specific IgG group (IgG RANKL group), Hey2-specific antibody control group (anti-Hey2 control group), Hey2-specific antibody group (anti-Hey2-RANKL group). For the different RANKL concentration groups and different induction time groups, real-time fluorescent quantitative PCR (RT-qPCR) was used to detect the mRNA expressions of nuclear factor of NFATc1, cathepsin K (CTSK), and cellular feline osteosarcoma oncogene (c-Fos) and tartrate-resistant acid phosphatase (TRAP) staining was used to assess the formation of multinucleated osteoclasts. After Hey2 overexpression or knockdown, RT-qPCR and Western blotting were used to detect the gene and protein expressions of NFATc1, c-Fos, and CTSK. TRAP staining was used to evaluate the formation of multinucleated osteoclasts. Bioinformatics prediction (NCBI, JASPAR) and chromatin immunoprecipitation (ChIP) assay were used to validate the binding of Hey2 to the NFATc1 promoter region. &lt;b&gt;Results:&lt;/b&gt; During the osteoclastic differentiation of RAW 264.7 cells induced by RANKL, the expression of Hey2 could be detected, and the expression level of Hey2 decreased with the increase of RANKL concentration and induction time. In the 50 μg/L RANKL group, the expression levels of Hey2 gene (0.18±0.00) and protein (0.22±0.02) were significantly lower than those in the control group (1.00±0.00, 0.52±0.01) (&lt;i&gt;t&lt;/i&gt;=41.67, 12.88; both &lt;i&gt;P&lt;/i&gt;&lt;0.001). In the 50 μg/L RANKL group inducted for 5 days, the expression levels of Hey2 gene (0.27±0.02) and protein (0.79±0.01) were significantly lower than those in the control group (1.00±0.00, 1.15±0.02) (&lt;i&gt;t&lt;/i&gt;=11.47, 108.60; both &lt;i&gt;P&lt;/i&gt;&lt;0.001). Hey2 overexpression significantly reduced the gene and protein expressions of NFATc1, c-Fos, and CTSK, as well as the production of TRAP-positive cells (all &lt;i&gt;P&lt;/i&gt;&lt;0.05). Hey2 knockdown significantly increased the gene and protein expressions of NFATc1, c-Fos, and CTSK, as well as the production of TRAP-positive cells (all &lt;i&gt;P&lt;/i&gt;&lt;0.05). After inducing RAW264.7 cells with 50 μg/L RANK","PeriodicalId":23965,"journal":{"name":"中华口腔医学杂志","volume":"60 11","pages":"1247-1256"},"PeriodicalIF":0.0,"publicationDate":"2025-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145439433","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Research progress in animal models of pulpitis]. 牙髓炎动物模型的研究进展
Q4 Medicine Pub Date : 2025-11-09 DOI: 10.3760/cma.j.cn112144-20250714-00264
K X Xu, L J Huo, R She, X Y Li, J Y Wu

Pulpitis is a prevalent inflammatory disease in dentistry, and root canal therapy remains the primary clinical treatment for it. However, pulp removal leads to reduced tooth fracture resistance and complications such as secondary infection and tooth fracture. As a potential alternative, vital pulp therapy (VPT) relies on precise assessment of pulp status; yet current clinical diagnostic methods lack specificity. The establishment of appropriate animal models for pulpitis is crucial for investigating its pathogenesis, developing specific diagnostic biomarkers, and optimizing VPT strategies. This review systematically summarizes experimental animals selection based on anatomical compatibility and pathological similarity, as well as model construction methods and multimodal evaluation systems for pulpitis animal models, aiming to provide insights for related researches.

牙髓炎是牙科学中一种常见的炎症性疾病,根管治疗仍是牙髓炎的主要临床治疗方法。然而,除牙髓会降低牙齿抗骨折能力,并减少继发感染和牙齿骨折等并发症。作为一种潜在的替代方法,重要牙髓治疗(VPT)依赖于对牙髓状态的精确评估;然而,目前的临床诊断方法缺乏特异性。建立合适的牙髓炎动物模型对于研究其发病机制、开发特异性诊断生物标志物和优化VPT策略至关重要。本文系统综述了基于解剖相容性和病理相似性的实验动物选择、牙髓炎动物模型构建方法和多模态评价体系,旨在为相关研究提供参考。
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引用次数: 0
[Latent profile analysis of body image and its influencing factors in postoperative oral cancer patients]. [口腔癌术后患者身体意象的潜在剖面分析及其影响因素]。
Q4 Medicine Pub Date : 2025-11-09 DOI: 10.3760/cma.j.cn112144-20250620-00230
Y Y Cao, X H Wang, J Qiu, X W Shi, Y Zhang, X Q Duan, L Cong

Objective: To analysis of the latent profiles and influencing factors of body image in patients with postoperative oral cancer. Methods: From July 2024 to March 2025, a total of 332 patients with primary oral cancer confirmed by pathology, aged ≥18 years, and undergoing oral cancer surgery at Hunan Cancer Hospital were selected using simple random sampling and cluster sampling. Among them, 25 were female and 307 were male. The body image scale and the Rosenberg self-esteem scale were used to investigate the patients. The main indicators included the total scale scores and scores on various dimensions of body image, such as appearance evaluation and health focus, with particular attention to satisfaction with facial appearance and oral function.The correlation between self-esteem and body image was analyzed, and differences in scores were compared based on gender, age, self-esteem level, and surgical procedure. Results: Among the 332 patients, 93.4% (310/332) were married, and 6.6% (22/332) were unmarried, divorced, or widowed. A total of 84.3% (280/332) underwent flap transplantation surgery, while 15.7% (52/332) did not. The body image distress in the 332 patients could be categorized into a body image adaptation group [80.12% (266/332)] and a body image disorder group [19.88% (66/332)]. Unmarried/divorced/widowed status (P=0.020), undergoing flap transplantation (P=0.006), and self-esteem level (P<0.001) were identified as influencing factors for postoperative body image disorder in oral cancer patients. Conclusions: Given the varying levels of body image concerns among oral cancer patients, healthcare providers can implement targeted, personalized nursing interventions based on their distinct categories and influencing factors.

目的:分析口腔癌术后患者身体形象的潜在特征及其影响因素。方法:采用简单随机抽样和整群抽样的方法,选取2024年7月至2025年3月在湖南省肿瘤医院经病理证实、年龄≥18岁并行口腔癌手术的原发性口腔癌患者332例。其中女性25人,男性307人。采用身体形象量表和Rosenberg自尊量表对患者进行调查。主要指标包括总量表得分和身体形象的各个维度得分,如外表评价和健康关注,特别关注面部外观和口腔功能的满意度。分析了自尊与身体形象之间的相关性,并比较了基于性别、年龄、自尊水平和手术方式的得分差异。结果:332例患者中已婚占93.4%(310/332),未婚、离婚、丧偶占6.6%(22/332)。84.3%(280/332)行皮瓣移植手术,15.7%(52/332)未行皮瓣移植手术。332例身体形象困扰患者可分为身体形象适应组[80.12%(266/332)]和身体形象障碍组[19.88%(66/332)]。结论:鉴于口腔癌患者对身体形象的关注程度不同,医疗服务提供者可根据其不同的类别和影响因素实施有针对性的个性化护理干预。
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引用次数: 0
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中华口腔医学杂志
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