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Application of stem cells in translational medicine. 干细胞在转化医学中的应用。
Pub Date : 2021-01-01 DOI: 10.12336/biomatertransl.2021.04.002
James T Triffitt, Qian Wang
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引用次数: 2
Role of hypoxia inducible factor 1α in cobalt nanoparticle induced cytotoxicity of human THP-1 macrophages. 缺氧诱导因子1α在钴纳米颗粒诱导人THP-1巨噬细胞毒性中的作用。
Pub Date : 2021-01-01 DOI: 10.12336/biomatertransl.2021.02.004
Wendy Rachel Francis, Zhao Liu, Sian E Owens, Xiao Wang, Huaming Xue, Alex Lord, Venkateswarlu Kanamarlapudi, Zhidao Xia, Zx, Wrf, Zx, Wrf, Zl, Wrf, Xw, Wrf, Seo, Xw, Hx, Al, Vk, Zl, Wrf, Zl, Al, Wrf, Zl, Vk, Zx

Cobalt is one of the main components of metal hip prostheses and cobalt nanoparticles (CoNPs) produced from wear cause inflammation, bone lyses and cytotoxicity at high concentrations. Cobalt ions mimic hypoxia in the presence of normal oxygen levels, and activate hypoxic signalling by stabilising hypoxia inducible transcription factor 1α (HIF1α). This study aimed to assess in vitro the functional role of HIF1α in CoNP induced cellular cytotoxicity. HIF1α, lysosomal pH, tumour necrosis factor α and interleukin 1β expression were analysed in THP-1 macrophages treated with CoNP (0, 10 and 100 μg/mL). HIF1α knock out assays were performed using small interfering RNA to assess the role of HIF1α in CoNP-induced cytotoxicity. Increasing CoNP concentration increased lysosomal activity and acidity in THP-1 macrophages. Higher doses of CoNP significantly reduced cell viability, stimulated caspase 3 activity and apoptosis. Reducing HIF1αactivity increased the pro-inflammatory activity of tumour necrosis factorαand interleukin 1β,but had no significant impact on cellular cytotoxicity. This suggests that whilst CoNP promotes cytotoxicity and cellular inflammation, the apoptotic mechanism is not dependent on HIF1α.

钴是金属髋关节假体的主要成分之一,磨损产生的钴纳米颗粒(CoNPs)在高浓度时会引起炎症、骨溶解和细胞毒性。钴离子在正常氧水平下模拟缺氧,并通过稳定缺氧诱导转录因子1α (HIF1α)激活缺氧信号。本研究旨在评估HIF1α在CoNP诱导的细胞毒性中的体外功能作用。检测CoNP(0、10、100 μg/mL)作用THP-1巨噬细胞中HIF1α、溶酶体pH、肿瘤坏死因子α和白细胞介素1β的表达。利用小干扰RNA进行HIF1α敲除实验,以评估HIF1α在conp诱导的细胞毒性中的作用。增加CoNP浓度可增加THP-1巨噬细胞的溶酶体活性和酸性。高剂量CoNP显著降低细胞活力,刺激caspase 3活性和细胞凋亡。降低hif α活性可提高肿瘤坏死因子α和白细胞介素1β的促炎活性,但对细胞毒性无显著影响。这表明,虽然CoNP促进细胞毒性和细胞炎症,但凋亡机制并不依赖于HIF1α。
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引用次数: 2
Focal adhesion regulates osteogenic differentiation of mesenchymal stem cells and osteoblasts. 局灶黏附调节间充质干细胞和成骨细胞的成骨分化。
Pub Date : 2021-01-01 DOI: 10.12336/biomatertransl.2021.04.007
Yang Zhao, Qing Sun, Bo Huo, Yz, Bh, Yz, Bh, Yz, Yz, Bh, Sq, Yz, Bh

Focal adhesions are large macromolecular assemblies through which cells are connected with the extracellular matrix so that extracellular signals can be transmitted inside cells. Some studies have focused on the effect of cell shape on the differentiation of stem cells, but little attention has been paid to focal adhesion. In the present study, mesenchymal stem cells (MSCs) and osteoblast-like MC3T3-E1 cells were seeded onto micropatterned substrates on which circular adhesive islands with different spacing and area were created for focal adhesion. Results showed that the patterns of focal adhesion changed cell morphology but did not affect cell survival. For MSCs cultured for 3 days, patterns with small circles and large spacing promoted osteogenesis. For MSCs cultured for 7 days, patterns with large circles and spacing enhanced osteogenesis. For MC3T3-E1 cells, the patterns of focal adhesion had no effect on cell differentiation after 3 days of culture, but patterns with small circles and spacing improved osteogenic differentiation after 7 days. Moreover, the assembly of F-actin, phosphorylation of myosin, and nuclear translocation of yes-associated proteins (YAP) were consistent with the expression of differentiation markers, indicating that the pattern of focal adhesion may affect the osteogenesis of MSCs and osteoblasts through changes in cytoskeletal tension and nuclear localisation of YAP.

局灶黏附是细胞与细胞外基质连接的大分子集合,细胞外信号可在细胞内传递。一些研究主要关注细胞形状对干细胞分化的影响,但对局灶黏附的研究很少。在本研究中,将间充质干细胞(MSCs)和成骨细胞样MC3T3-E1细胞植入微图纹基质上,在微图纹基质上建立具有不同间距和面积的圆形粘附岛以进行局部粘附。结果表明,局灶黏附模式改变了细胞形态,但不影响细胞存活。对于培养3 d的MSCs,小圆和大间距的图案促进成骨。对于培养7天的MSCs,大圆圈和间距的图案促进成骨。对于MC3T3-E1细胞,在培养3天后,局灶黏附模式对细胞分化没有影响,但在培养7天后,小圆圈和间距模式促进了成骨分化。此外,F-actin的组装、myosin的磷酸化和yes-associated protein (YAP)的核易位与分化标志物的表达一致,表明局灶性粘连的模式可能通过改变细胞骨架张力和YAP的核定位来影响MSCs和成骨细胞的成骨。
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引用次数: 5
Engineering immune-responsive biomaterials for skin regeneration. 皮肤再生的工程免疫应答生物材料。
Pub Date : 2021-01-01 DOI: 10.3877/cma.j.issn.2096-112X.2021.01.008
Pingli Wu, Yangyang Liang, Guoming Sun, Pw, Gs, Gs, Pw, Yl, Yl

The progress of biomaterials and tissue engineering has led to significant advances in wound healing, but the clinical therapy to regenerate perfect skin remains a great challenge. The implantation of biomaterial scaffolds to heal wounds inevitably leads to a host immune response. Many recent studies revealed that the immune system plays a significant role in both the healing process and the outcome. Immunomodulation or immuno-engineering has thus become a promising approach to develop pro-regenerative scaffolds for perfect skin regeneration. In this paper, we will review recent advancements in immunomodulating biomaterials in the field of skin repair and regeneration, and discuss strategies to modulate the immune response by tailoring the chemical, physical and biological properties of the biomaterials. Understanding the important role of immune responses and manipulating the inherent properties of biomaterials to regulate the immune reaction are approaches to overcome the current bottleneck of skin repair and regeneration.

生物材料和组织工程的进步使伤口愈合取得了重大进展,但临床治疗再生完美皮肤仍然是一个巨大的挑战。植入生物材料支架治疗伤口不可避免地会引起宿主的免疫反应。最近的许多研究表明,免疫系统在愈合过程和结果中都起着重要作用。因此,免疫调节或免疫工程已成为开发促再生支架以实现完美皮肤再生的一种有前途的方法。本文将综述免疫调节生物材料在皮肤修复和再生领域的最新进展,并讨论通过调整生物材料的化学、物理和生物特性来调节免疫反应的策略。了解免疫反应的重要作用,利用生物材料的固有特性来调节免疫反应是克服当前皮肤修复和再生瓶颈的途径。
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引用次数: 11
Human pluripotent stem cells: tools for regenerative medicine. 人类多能干细胞:再生医学的工具。
Pub Date : 2021-01-01 DOI: 10.12336/biomatertransl.2021.04.004
Peter W Andrews, Pwa

Human embryonic stem cells and induced pluripotent stem cells, together denoted as pluripotent stem cells have opened up unprecedented opportunities for developments in human healthcare over the past 20 years. Although much about the properties and behaviour of these cells required to underpin their applications has been discovered over this time, a number of issues remain. This brief review considers the history of these developments and some of the underlying biology, pointing out some of the problems still to be resolved, particularly in relation to their genetic stability and possible malignancy.

人类胚胎干细胞和诱导多能干细胞,统称为多能干细胞,在过去20年中为人类医疗保健的发展开辟了前所未有的机遇。尽管在此期间已经发现了支持其应用所需的这些细胞的许多特性和行为,但仍存在许多问题。这篇简短的综述考虑了这些发展的历史和一些潜在的生物学,指出了一些仍有待解决的问题,特别是与它们的遗传稳定性和可能的恶性有关。
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引用次数: 4
Surface topography and free energy regulate osteogenesis of stem cells: effects of shape-controlled gold nanoparticles. 表面形貌和自由能调节干细胞成骨:形状控制金纳米颗粒的影响。
Pub Date : 2021-01-01 DOI: 10.12336/biomatertransl.2021.02.006
Kamolrat Metavarayuth, Esteban Villarreal, Hui Wang, Qian Wang, Hw, Qw, Mk, Ev, Mk, Mk, Hw, Qw, Mk, Hw, Qw

The surface free energy of a biomaterial plays an important role in the early stages of cell-biomaterial interactions, profoundly influencing protein adsorption, interfacial water accessibility, and cell attachment on the biomaterial surface. Although multiple approaches have been developed to engineer the surface free energy of biomaterials, systematically tuning their surface free energy without altering other physicochemical properties remains challenging. In this study, we constructed an array of chemically-equivalent surfaces with comparable apparent roughness through assembly of gold nanoparticles adopting various geometrically-distinct shapes but all capped with the same surface ligand, (1-hexadecyl)trimethylammonium chloride, on cell culture substrates. We found that bone marrow stem cells exhibited distinct osteogenic differentiation behaviours when interacting with different types of substrates comprising shape-controlled gold nanoparticles. Our results reveal that bone marrow stem cells are capable of sensing differences in the nanoscale topographical features, which underscores the role of the surface free energy of nanostructured biomaterials in regulating cell responses. The study was approved by Institutional Animal Care and Use Committee, School of Medicine, University of South Carolina.

生物材料的表面自由能在细胞-生物材料相互作用的早期阶段起着重要的作用,深刻地影响着蛋白质吸附、界面水可及性和细胞在生物材料表面的附着。虽然已经开发了多种方法来设计生物材料的表面自由能,但在不改变其他物理化学性质的情况下系统地调整其表面自由能仍然是一项挑战。在本研究中,我们通过在细胞培养基质上组装具有不同几何形状的金纳米颗粒,构建了一系列具有相当表面粗糙度的化学等效表面,这些表面具有相同的表面配体(1-十六烷基)三甲基氯化铵。我们发现骨髓干细胞在与不同类型的含有形状控制金纳米颗粒的基质相互作用时表现出不同的成骨分化行为。我们的研究结果表明,骨髓干细胞能够感知纳米尺度地形特征的差异,这强调了纳米结构生物材料的表面自由能在调节细胞反应中的作用。该研究得到了南卡罗来纳大学医学院动物护理和使用机构委员会的批准。
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引用次数: 3
In silico modelling of the corrosion of biodegradable magnesium-based biomaterials: modelling approaches, validation and future perspectives. 可生物降解镁基生物材料腐蚀的硅模拟:模拟方法、验证和未来展望。
Pub Date : 2021-01-01 DOI: 10.12336/biomatertransl.2021.03.008
Aditya Joshi, George Dias, Mark P Staiger, Aj, Mps, Gd

Metallic biomedical implants based on magnesium, zinc and iron alloys have emerged as bioresorbable alternatives to permanent orthopaedic implants over the last two decades. The corrosion rate of biodegradable metals plays a critical role in controlling the compatibility and functionality of the device in vivo. The broader adoption of biodegradable metals in orthopaedic applications depends on developing in vitro methods that accurately predict the biodegradation behaviour in vivo. However, the physiological environment is a highly complex corrosion environment to replicate in the laboratory, making the in vitro-to-in vivo translation of results very challenging. Accordingly, the results from in vitro corrosion tests fail to provide a complete schema of the biodegradation behaviour of the metal in vivo. In silico approach based on computer simulations aim to bridge the observed differences between experiments performed in vitro and vivo. A critical review of the state-of-the-art of computational modelling techniques for predicting the corrosion behaviour of magnesium alloy as a biodegradable metal is presented.

在过去的二十年里,基于镁、锌和铁合金的金属生物医学植入物已经成为永久性骨科植入物的生物可吸收替代品。生物可降解金属的腐蚀速率对控制器件在体内的相容性和功能起着至关重要的作用。生物可降解金属在骨科应用中的广泛应用取决于开发出能够准确预测体内生物降解行为的体外方法。然而,生理环境是一个高度复杂的腐蚀环境,在实验室中复制,使得在体外到体内的结果翻译非常具有挑战性。因此,体外腐蚀试验的结果不能提供金属在体内生物降解行为的完整模式。基于计算机模拟的计算机方法旨在弥合在体外和体内进行的实验之间观察到的差异。对预测镁合金作为可生物降解金属的腐蚀行为的计算建模技术的最新进展进行了评述。
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引用次数: 1
Magnesium-based materials in orthopaedics: material properties and animal models. 骨科用镁基材料:材料特性和动物模型。
Pub Date : 2021-01-01 DOI: 10.12336/biomatertransl.2021.03.004
Xirui Jing, Qiuyue Ding, Qinxue Wu, Weijie Su, Keda Yu, Yanlin Su, Bing Ye, Qing Gao, Tingfang Sun, Xiaodong Guo, Xj, Ts, Xg, Xj, Xj, Qd, Ws, Ky, Xj, Qd, Ws, Ky, Ys, By, Qw, Qg, Ts, Xj, Qd, Ws, Ky, Xj, Xj, Qd, Ws, Ky, Xj, Qd, Ws, Ky, Ys, Xg

As a new generation of medical metal materials, degradable magnesium-based materials have excellent mechanical properties and osteogenic promoting ability, making them promising materials for the treatment of refractory bone diseases. Animal models can be used to understand and evaluate the performance of materials in complex physiological environments, providing relevant data for preclinical evaluation of implants and laying the foundation for subsequent clinical studies. To date, many researchers have studied the biocompatibility, degradability and osteogenesis of magnesium-based materials, but there is a lack of review regarding the effects of magnesium-based materials in vivo. In view of the growing interest in these materials, this review briefly describes the properties of magnesium-based materials and focuses on the safety and efficacy of magnesium-based materials in vivo. Various animal models including rats, rabbits, dogs and pigs are covered to better understand and evaluate the progress and future of magnesium-based materials. This literature analysis reveals that the magnesium-based materials have good biocompatibility and osteogenic activity, thus causing no adverse reaction around the implants in vivo, and that they exhibit a beneficial effect in the process of bone repair. In addition, the degradation rate in vivo can also be improved by means of alloying and coating. These encouraging results show a promising future for the use of magnesium-based materials in musculoskeletal disorders.

可降解镁基材料作为新一代医用金属材料,具有优异的力学性能和促进成骨的能力,是治疗难治性骨病的理想材料。利用动物模型可以了解和评估材料在复杂生理环境下的性能,为植入物的临床前评估提供相关数据,为后续临床研究奠定基础。迄今为止,许多研究者对镁基材料的生物相容性、可降解性和成骨性进行了研究,但缺乏对镁基材料在体内作用的综述。鉴于人们对镁基材料的兴趣日益浓厚,本文简要介绍了镁基材料的性能,并重点介绍了镁基材料在体内的安全性和有效性。包括大鼠、兔子、狗和猪在内的各种动物模型,以更好地了解和评估镁基材料的进展和未来。本文献分析表明,镁基材料具有良好的生物相容性和成骨活性,在体内对种植体周围无不良反应,在骨修复过程中表现出有益的作用。此外,还可以通过合金化和涂层等手段提高其在体内的降解率。这些令人鼓舞的结果表明,镁基材料在肌肉骨骼疾病中的应用前景广阔。
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引用次数: 9
Recombinant adeno-associated virus-based gene therapy combined with tissue engineering for musculoskeletal regenerative medicine. 重组腺相关病毒基因治疗联合组织工程用于肌肉骨骼再生医学。
Pub Date : 2021-01-01 DOI: 10.3877/cma.j.issn.2096-112X.2021.01.004
Yiqing Wang, Xiangyu Chu, Bing Wang, Yw, Bw, Xc, Bw

Recombinant adeno-associated viral (rAAV) vector-mediated gene delivery is a novel molecular therapeutic approach for musculoskeletal disorders which achieves tissue regeneration by delivering a transgene to the impaired tissue. In recent years, substantial scientific progress in rAAV gene therapy has led to several clinical trials for human musculoskeletal diseases. Nevertheless, there are still limitations in developing an optimal gene therapy model due to the low transduction efficiency and fast degradation of the gene vectors. To overcome the challenges of rAAV gene therapy, tissue engineering combined with gene therapy has emerged as a more promising alternative. An rAAV viral vector incorporated into a biomaterial has a more controlled gene expression, lower immune response, and higher efficiency. A number of biomaterials and architectures have been combined with rAAV viral vectors, each having its own advantages and limitations. This review aims to give a broad introduction to combinatorial therapy and the recent progress this new technology has offered.

重组腺相关病毒(rAAV)载体介导的基因传递是一种新的肌肉骨骼疾病的分子治疗方法,它通过向受损组织传递转基因来实现组织再生。近年来,rAAV基因治疗取得了实质性的科学进展,导致了几项针对人类肌肉骨骼疾病的临床试验。然而,由于基因载体的转导效率低,降解快,在开发最佳的基因治疗模型方面仍然存在局限性。为了克服rAAV基因治疗的挑战,组织工程结合基因治疗已成为一种更有前途的替代方案。将rAAV病毒载体整合到生物材料中,具有更可控的基因表达、更低的免疫反应和更高的效率。许多生物材料和结构已经与rAAV病毒载体结合,每种都有其自身的优点和局限性。这篇综述的目的是给一个广泛的介绍联合治疗和这项新技术的最新进展。
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引用次数: 2
Physicochemical properties of respiratory droplets and their role in COVID-19 pandemics: a critical review. 呼吸道飞沫的物理化学性质及其在COVID-19大流行中的作用:一项重要综述
Pub Date : 2021-01-01 DOI: 10.3877/cma.j.issn.2096-112X.2021.01.003
Ting Ge, Shengfeng Cheng, Tg

The ongoing coronavirus disease 2019 (COVID-19) pandemic is a serious challenge faced by the global community. Physical scientists can help medical workers and biomedical scientists, engineers, and practitioners, who are working on the front line, to slow down and eventually contain the spread of the COVID-19 virus. This review is focused on the physicochemical characteristics, including composition, aerodynamics, and drying behavior of respiratory droplets as a complex and multicomponent soft matter system, which are the main carrier of the virus for interpersonal transmission. The distribution and dynamics of virus particles within a droplet are also discussed. Understanding the characteristics of virus-laden respiratory droplets can lead to better design of personal protective equipment, frequently touched surfaces such as door knobs and touchscreens, and filtering equipment for indoor air circulation. Such an understanding also provides the scientific basis of public policy, including social distancing rules and public hygiene guidelines, implemented by governments around the world.

正在发生的2019冠状病毒病(COVID-19)大流行是国际社会面临的严峻挑战。物理科学家可以帮助在第一线工作的医务工作者、生物医学科学家、工程师和从业人员减缓并最终遏制COVID-19病毒的传播。本文综述了作为病毒人际传播主要载体的呼吸道飞沫作为一个复杂的多组分软物质系统的物理化学特征,包括组成、空气动力学和干燥行为。还讨论了病毒颗粒在液滴内的分布和动力学。了解携带病毒的呼吸道飞沫的特征,可以更好地设计个人防护装备,经常接触的表面,如门把手和触摸屏,以及室内空气循环的过滤设备。这种认识也为世界各国政府实施的公共政策提供了科学依据,包括保持社会距离规则和公共卫生准则。
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引用次数: 3
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Biomaterials Translational
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