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      The marriage of immunomodulatory, angiogenic, and osteogenic capabilities in a piezoelectric hydrogel tissue engineering scaffold for military medicine

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          Abstract

          Background

          Most bone-related injuries to grassroots troops are caused by training or accidental injuries. To establish preventive measures to reduce all kinds of trauma and improve the combat effectiveness of grassroots troops, it is imperative to develop new strategies and scaffolds to promote bone regeneration.

          Methods

          In this study, a porous piezoelectric hydrogel bone scaffold was fabricated by incorporating polydopamine (PDA)-modified ceramic hydroxyapatite (PDA-hydroxyapatite, PHA) and PDA-modified barium titanate (PDA-BaTiO 3, PBT) nanoparticles into a chitosan/gelatin (Cs/Gel) matrix. The physical and chemical properties of the Cs/Gel/PHA scaffold with 0–10 wt% PBT were analyzed. Cell and animal experiments were performed to characterize the immunomodulatory, angiogenic, and osteogenic capabilities of the piezoelectric hydrogel scaffold in vitro and in vivo.

          Results

          The incorporation of BaTiO 3 into the scaffold improved its mechanical properties and increased self-generated electricity. Due to their endogenous piezoelectric stimulation and bioactive constituents, the as-prepared Cs/Gel/PHA/PBT hydrogels exhibited cytocompatibility as well as immunomodulatory, angiogenic, and osteogenic capabilities; they not only effectively induced macrophage polarization to M2 phenotype but also promoted the migration, tube formation, and angiogenic differentiation of human umbilical vein endothelial cells (HUVECs) and facilitated the migration, osteo-differentiation, and extracellular matrix (ECM) mineralization of MC3T3-E1 cells. The in vivo evaluations showed that these piezoelectric hydrogels with versatile capabilities significantly facilitated new bone formation in a rat large-sized cranial injury model. The underlying molecular mechanism can be partly attributed to the immunomodulation of the Cs/Gel/PHA/PBT hydrogels as shown via transcriptome sequencing analysis, and the PI3K/Akt signaling axis plays an important role in regulating macrophage M2 polarization.

          Conclusion

          The piezoelectric Cs/Gel/PHA/PBT hydrogels developed here with favorable immunomodulation, angiogenesis, and osteogenesis functions may be used as a substitute in periosteum injuries, thereby offering the novel strategy of applying piezoelectric stimulation in bone tissue engineering for the enhancement of combat effectiveness in grassroots troops.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s40779-023-00469-5.

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          Most cited references70

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          Flexible Nanogenerators for Energy Harvesting and Self-Powered Electronics.

          Flexible nanogenerators that efficiently convert mechanical energy into electrical energy have been extensively studied because of their great potential for driving low-power personal electronics and self-powered sensors. Integration of flexibility and stretchability to nanogenerator has important research significance that enables applications in flexible/stretchable electronics, organic optoelectronics, and wearable electronics. Progress in nanogenerators for mechanical energy harvesting is reviewed, mainly including two key technologies: flexible piezoelectric nanogenerators (PENGs) and flexible triboelectric nanogenerators (TENGs). By means of material classification, various approaches of PENGs based on ZnO nanowires, lead zirconate titanate (PZT), poly(vinylidene fluoride) (PVDF), 2D materials, and composite materials are introduced. For flexible TENG, its structural designs and factors determining its output performance are discussed, as well as its integration, fabrication and applications. The latest representative achievements regarding the hybrid nanogenerator are also summarized. Finally, some perspectives and challenges in this field are discussed.
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            Fracture healing: mechanisms and interventions.

            Fractures are the most common large-organ, traumatic injuries to humans. The repair of bone fractures is a postnatal regenerative process that recapitulates many of the ontological events of embryonic skeletal development. Although fracture repair usually restores the damaged skeletal organ to its pre-injury cellular composition, structure and biomechanical function, about 10% of fractures will not heal normally. This article reviews the developmental progression of fracture healing at the tissue, cellular and molecular levels. Innate and adaptive immune processes are discussed as a component of the injury response, as are environmental factors, such as the extent of injury to the bone and surrounding tissue, fixation and the contribution of vascular tissues. We also present strategies for fracture treatment that have been tested in animal models and in clinical trials or case series. The biophysical and biological basis of the molecular actions of various therapeutic approaches, including recombinant human bone morphogenetic proteins and parathyroid hormone therapy, are also discussed.
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              Periosteal matrix-derived hydrogel promotes bone repair through an early immune regulation coupled with enhanced angio- and osteogenesis

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                Author and article information

                Contributors
                wuping@wmu.edu.cn
                lin_shen168@163.com
                liuhuifan5@163.com
                2623830207@qq.com
                juanzhaohh@163.com
                1830157159@qq.com
                929788786@qq.com
                zli40@keuka.edu
                1421606840@qq.com
                luolihua81@126.com
                zhiqiangluo@hust.edu.cn
                wuminhao1991@whu.edu.cn
                orthopedics@whu.edu.cn
                xiaokunli@wmu.edu.cn
                wzhouguang@gmail.com
                Journal
                Mil Med Res
                Mil Med Res
                Military Medical Research
                BioMed Central (London )
                2095-7467
                2054-9369
                31 July 2023
                31 July 2023
                2023
                : 10
                : 35
                Affiliations
                [1 ]GRID grid.268099.c, ISNI 0000 0001 0348 3990, Key Laboratory of Imaging Diagnosis and Minimally Invasive Intervention Research, the Fifth Affiliated Hospital of Wenzhou Medical University, ; Lishui, 323000 Zhejiang China
                [2 ]GRID grid.268099.c, ISNI 0000 0001 0348 3990, Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine, Vision and Brain Health), School of Pharmaceutical Science, , Wenzhou Medical University, ; Wenzhou, 325000 Zhejiang China
                [3 ]GRID grid.413247.7, ISNI 0000 0004 1808 0969, Department of Spine Surgery and Musculoskeletal Tumor, , Zhongnan Hospital of Wuhan University, ; Wuhan, 430071 China
                [4 ]GRID grid.33199.31, ISNI 0000 0004 0368 7223, National Engineering Research Center for Nanomedicine, College of Life Science and Technology, , Huazhong University of Science and Technology, ; Wuhan, 430074 China
                [5 ]GRID grid.411902.f, ISNI 0000 0001 0643 6866, Department of Overseas Education College, , Jimei University, ; Xiamen, 361021 Fujian China
                [6 ]GRID grid.268099.c, ISNI 0000 0001 0348 3990, School and Hospital of Stomatology, , Wenzhou Medical University, ; Wenzhou, 325035 Zhejiang China
                Author information
                http://orcid.org/0000-0001-7374-6506
                Article
                469
                10.1186/s40779-023-00469-5
                10388535
                37525300
                5a6f29e1-a70d-4c9c-8608-90b41b3d0bd4
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 4 April 2023
                : 5 July 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 82202352
                Award ID: 82271629
                Award Recipient :
                Funded by: Translational Medicine and Interdisciplinary Research Joint Fund of Zhongnan Hospital of Wuhan University
                Award ID: ZNLH202202
                Funded by: Wenzhou Medical University grant
                Award ID: QTJ23004
                Categories
                Research
                Custom metadata
                © People´s Military Medical Press 2023

                piezoelectric hydrogel,tissue engineering scaffold,immunomodulation,angiogenesis,osteogenic differentiation

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