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1
Dual Affinity Heparin-Based Hydrogels Achieve Pro-Regenerative Immunomodulation and Microvascular Remodeling.基于双亲和性肝素的水凝胶实现促再生免疫调节和微血管重塑。
ACS Biomater Sci Eng. 2018 Apr 9;4(4):1241-1250. doi: 10.1021/acsbiomaterials.6b00706. Epub 2017 Feb 20.
2
Intra-articular TSG-6 delivery from heparin-based microparticles reduces cartilage damage in a rat model of osteoarthritis.基于肝素的微球腔内递送 TSG-6 可减少骨关节炎大鼠模型的软骨损伤。
Biomater Sci. 2018 May 1;6(5):1159-1167. doi: 10.1039/C8BM00010G.
3
Quantitative analysis of immune cell subset infiltration of supraspinatus muscle after severe rotator cuff injury.严重肩袖损伤后冈上肌免疫细胞亚群浸润的定量分析
Regen Eng Transl Med. 2017 Jun;3(2):82-93. doi: 10.1007/s40883-017-0030-2. Epub 2017 May 8.
4
Delivery of stromal cell-derived factor 1α for tissue regeneration.用于组织再生的基质细胞衍生因子1α的递送
J Biol Eng. 2017 Jun 29;11:22. doi: 10.1186/s13036-017-0058-3. eCollection 2017.
5
Non-classical monocytes are biased progenitors of wound healing macrophages during soft tissue injury.非经典单核细胞是软组织损伤过程中伤口愈合巨噬细胞的偏向性祖细胞。
Sci Rep. 2017 Mar 27;7(1):447. doi: 10.1038/s41598-017-00477-1.
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Core-shell microparticles for protein sequestration and controlled release of a protein-laden core.用于蛋白质螯合和载有蛋白质的核心的控释的核壳微粒。
Acta Biomater. 2017 Jul 1;56:91-101. doi: 10.1016/j.actbio.2016.12.042. Epub 2016 Dec 21.
7
Hydrolysis and Sulfation Pattern Effects on Release of Bioactive Bone Morphogenetic Protein-2 from Heparin-Based Microparticles.水解和硫酸化模式对基于肝素的微粒释放生物活性骨形态发生蛋白-2的影响。
J Mater Chem B. 2015 Oct 28;3(40):8001-8009. doi: 10.1039/C5TB00933B. Epub 2015 Aug 28.
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Heparin-based hydrogels with tunable sulfation & degradation for anti-inflammatory small molecule delivery.具有可调节硫酸化和降解特性的肝素基水凝胶用于抗炎小分子递送。
Biomater Sci. 2016 Aug 16;4(9):1371-80. doi: 10.1039/c6bm00455e.
9
Monocytes and macrophages in tissue repair: Implications for immunoregenerative biomaterial design.组织修复中的单核细胞和巨噬细胞:对免疫再生生物材料设计的启示。
Exp Biol Med (Maywood). 2016 May;241(10):1084-97. doi: 10.1177/1535370216650293.
10
Spatially localized recruitment of anti-inflammatory monocytes by SDF-1α-releasing hydrogels enhances microvascular network remodeling.通过释放SDF-1α的水凝胶对抗炎单核细胞进行空间定位募集可增强微血管网络重塑。
Biomaterials. 2016 Jan;77:280-90. doi: 10.1016/j.biomaterials.2015.10.045. Epub 2015 Oct 23.

严重肩袖损伤后,局部递送基质细胞衍生因子-1α可增加冈上肌中促进愈合的骨髓来源细胞。

Localized SDF-1α Delivery Increases Pro-Healing Bone Marrow-Derived Cells in the Supraspinatus Muscle Following Severe Rotator Cuff Injury.

作者信息

Tellier L E, Krieger J R, Brimeyer A L, Coogan A C, Falis A A, Rinker T E, Schudel A, Thomas S N, Jarrett C D, Willett N J, Botchwey E A, Temenoff J S

机构信息

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA.

School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, GA.

出版信息

Regen Eng Transl Med. 2018 Jun;4(2):92-103. doi: 10.1007/s40883-018-0052-4. Epub 2018 Apr 23.

DOI:10.1007/s40883-018-0052-4
PMID:30288396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6166879/
Abstract

To examine how the chemotactic agent stromal cell-derived factor-1alpha (SDF-1α) modulates the unique cellular milieu within rotator cuff muscle following tendon injury, we developed an injectable, heparin-based microparticle platform to locally present SDF-1α within the supraspinatus muscle following severe rotator cuff injury. SDF-1α loaded, degradable, N-desulfated heparin-based microparticles were fabricated, injected into a rat model of severe rotator cuff injury, and were retained for up to 7 days at the site. The resultant inflammatory cell and mesenchymal stem cell populations were analyzed compared to uninjured contralateral controls and, after 7 days, the fold-change in anti-inflammatory, M2-like macrophages (CD11b+CD68+CD163+, 4.3X fold-change) and mesenchymal stem cells (CD29+CD44+CD90+, 3.0X, respectively) was significantly greater in muscles treated with SDF-1α loaded microparticles than unloaded microparticles or injury alone. Our results indicate that SDF-1α loaded microparticles may be a novel approach to shift the cellular composition within the supraspinatus muscle and create a more pro-regenerative milieu, which may provide a platform to improve muscle repair following rotator cuff injury in the future.

摘要

为了研究趋化因子基质细胞衍生因子-1α(SDF-1α)如何调节肌腱损伤后肩袖肌内独特的细胞环境,我们开发了一种可注射的、基于肝素的微粒平台,以便在严重肩袖损伤后将SDF-1α局部递送至冈上肌内。制备了负载SDF-1α的、可降解的、N-去硫酸化的基于肝素的微粒,将其注射到严重肩袖损伤的大鼠模型中,并在注射部位保留长达7天。将所得的炎症细胞和间充质干细胞群体与未受伤的对侧对照进行分析比较,7天后,在注射负载SDF-1α微粒的肌肉中,抗炎性、M2样巨噬细胞(CD11b+CD68+CD163+,变化倍数为4.3倍)和间充质干细胞(CD29+CD44+CD90+,变化倍数分别为3.0倍)的变化倍数显著高于注射未负载微粒的肌肉或仅受伤的肌肉。我们的结果表明,负载SDF-1α的微粒可能是一种改变冈上肌细胞组成并创造更有利于再生环境的新方法,这可能为未来改善肩袖损伤后的肌肉修复提供一个平台。