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通过利用 c-Jun N-末端激酶 3 的年龄改变的激活来加速体内骨愈合。

Accelerating bone healing in vivo by harnessing the age-altered activation of c-Jun N-terminal kinase 3.

机构信息

Tissue Engineering Research Group, Department of Anatomy and Regenerative Medicine, Royal College of Surgeons in Ireland (RCSI), Dublin 2 D02 YN77, Ireland; Advanced Materials Bio-Engineering Research Centre (AMBER), RCSI and TCD, Dublin 2 D02 PN40, Ireland.

Tissue Engineering Research Group, Department of Anatomy and Regenerative Medicine, Royal College of Surgeons in Ireland (RCSI), Dublin 2 D02 YN77, Ireland; Trinity Centre for Biomedical Engineering, Trinity Biomedical Sciences Institute, Trinity College Dublin (TCD), Dublin 2 D02 PN40, Ireland.

出版信息

Biomaterials. 2021 Jan;268:120540. doi: 10.1016/j.biomaterials.2020.120540. Epub 2020 Nov 27.

Abstract

We have recently demonstrated that c-Jun N-terminal kinase 3 (JNK3) is a key modulator of the enhanced osteogenic potential of stem cells derived from children when compared to those derived from adults. In this study, we formulated a JNK3-activator nanoparticle (JNK3*) that recapitulates the immense osteogenic potential of juvenile cells in adult stem cells by facilitating JNK3 activation. Moreover, we aimed to functionalize a collagen-based scaffold by incorporating the JNK3* in order to develop an advanced platform capable of accelerating bone healing by recruitment of host stem cells. Our data, in vitro and in vivo, demonstrated that the immense osteogenic potential of juvenile cells could be recapitulated in adult stem cells by facilitating JNK3 activation. Moreover, our results revealed that the JNK3* functionalized 3D scaffold induced the fastest bone healing and greatest blood vessel infiltration when implanted in critical-size rat calvarial defects in vivo. JNK3*scaffold fastest bone healing in vivo was associated with its capacity to recruit host stem cells to the site of injury and promote angiogenic-osteogenic coupling (e.g. Vegfa, Tie1, Runx2, Alp and Igf2 upregulation). In summary, this study has demonstrated the potential of harnessing knowledge of age-altered stem cell mechanobiology in order to develop a materials-based functionalization approach for the repair of large tissue defects.

摘要

我们最近证明,与成人来源的干细胞相比,c-Jun N 端激酶 3(JNK3)是儿童来源的干细胞增强成骨潜能的关键调节因子。在这项研究中,我们设计了一种 JNK3 激活剂纳米颗粒(JNK3*),通过促进 JNK3 激活来重现幼年细胞巨大的成骨潜能。此外,我们旨在通过将 JNK3掺入胶原基支架中来对其进行功能化,从而开发一种能够通过募集宿主干细胞来加速骨愈合的先进平台。我们的体外和体内数据表明,通过促进 JNK3 激活可以在成人干细胞中重现幼年细胞巨大的成骨潜能。此外,我们的结果表明,当植入大鼠颅骨临界大小缺损的体内时,JNK3功能化的 3D 支架可诱导最快的骨愈合和最大的血管浸润。JNK3*支架在体内的最快骨愈合与其招募宿主干细胞到损伤部位并促进血管生成和成骨偶联的能力(例如 Vegfa、Tie1、Runx2、Alp 和 Igf2 的上调)有关。总之,这项研究表明,利用年龄改变的干细胞机械生物学知识来开发基于材料的功能化方法修复大组织缺陷具有潜力。

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