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受生理学启发的多层纳米纤维膜调控内源性干细胞募集和成骨分化用于分阶段骨再生。

Physiology-Inspired Multilayer Nanofibrous Membranes Modulating Endogenous Stem Cell Recruitment and Osteo-Differentiation for Staged Bone Regeneration.

机构信息

Department of Orthopedics, The First Affiliated Hospital, School of Life Science, Bengbu Medical College, Bengbu, 233030, China.

Anhui Province Key Laboratory of Tissue Transplantation, Bengbu Medical College, Bengbu, 233030, China.

出版信息

Adv Healthc Mater. 2022 Nov;11(21):e2201457. doi: 10.1002/adhm.202201457. Epub 2022 Sep 2.

DOI:10.1002/adhm.202201457
PMID:36027596
Abstract

Bone regeneration involves a cascade of sophisticated, multiple-staged cellular and molecular events, where early-phase stem cell recruitment mediated by chemokines and late-phase osteo-differentiation induced by pro-osteogenic factors play the crucial roles. Herein, enlightened by a bone physiological and regenerative mechanism, the multilayer nanofibrous membranes (PLLA@SDF-1α@MT01) consisting of PLLA/MT01 micro-sol electrospun nanofibers as intima and PLLA/PEG/SDF-1α electrospun nanofibers as adventitia are fabricated through micro-sol electrospinning and manual multi-layer stacking technologies. In vitro releasing profiles show that PLLA@SDF-1α@MT01 represents the rapid release of stromal cell-derived SDF-1α (SDF-1α) in the outer layers, while with long-term sustained release of MT01 in the inner layer. Owing to interconnected porosity like the natural bone extracellular matrix and improved hydrophilia, PLLA@SDF-1α@MT01 manifests good biocompatibility both in vitro and in vivo. Furthermore, PLLA@SDF-1α@MT01 can promote bone marrow mesenchymal stem cells (BMSCs) migration by amplifying the SDF-1α/CXCR4 axis and stimulating BMSCs osteo-differentiation via activating the MAPK pathway in vitro. PLLA@SDF-1α@MT01, with a programmed dual-delivery system, exhibits the synergetic promotion of bone regeneration and vascularization by emulating key characteristics of the staged bone repair in vivo. Overall, PLLA@SDF-1α@MT01 that mimics the endogenous cascades of bone regeneration can enrich the physiology-mimetic staged regenerative strategy and represent a promising tissue-engineered scaffold for the bone defect.

摘要

骨再生涉及一系列复杂的、多阶段的细胞和分子事件,其中趋化因子介导的早期干细胞募集和前成骨因子诱导的晚期成骨分化起着关键作用。在此,受骨生理和再生机制的启发,通过微溶胶静电纺丝和手动多层堆叠技术制备了由 PLLA/MT01 微溶胶静电纺纳米纤维作为内膜和 PLLA/PEG/SDF-1α 静电纺纳米纤维作为外膜组成的多层纳米纤维膜(PLLA@SDF-1α@MT01)。体外释放曲线表明,PLLA@SDF-1α@MT01 在外层表现出基质细胞衍生的 SDF-1α(SDF-1α)的快速释放,而在内层则表现出 MT01 的长期持续释放。由于具有类似于天然骨细胞外基质的互联孔隙率和提高的亲水性,PLLA@SDF-1α@MT01 在体外和体内均表现出良好的生物相容性。此外,PLLA@SDF-1α@MT01 可以通过放大 SDF-1α/CXCR4 轴促进骨髓间充质干细胞(BMSCs)迁移,并通过体外激活 MAPK 通路刺激 BMSCs 成骨分化。PLLA@SDF-1α@MT01 具有程控双输送系统,通过模拟体内分期骨修复的关键特征,表现出协同促进骨再生和血管化的作用。总之,模仿内源性骨再生级联反应的 PLLA@SDF-1α@MT01 可以丰富生理模拟分期再生策略,并为骨缺损提供有前途的组织工程支架。

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