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本文引用的文献

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Anti-donor immune responses elicited by allogeneic mesenchymal stem cells: what have we learned so far?同种异体间充质干细胞引发的抗供体免疫反应:我们迄今为止学到了什么?
Immunol Cell Biol. 2013 Jan;91(1):40-51. doi: 10.1038/icb.2012.67. Epub 2012 Dec 4.
2
Impaired biomechanical properties correlate with neoangiogenesis as well as VEGF and MMP-3 expression during rat patellar tendon healing.在大鼠髌腱愈合过程中,生物力学性能的受损与新生血管形成以及 VEGF 和 MMP-3 的表达相关。
J Orthop Res. 2012 Dec;30(12):1952-7. doi: 10.1002/jor.22147. Epub 2012 May 21.
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Interleukin-1 beta influences on lysyl oxidases and matrix metalloproteinases profile of injured anterior cruciate ligament and medial collateral ligament fibroblasts.白细胞介素-1β对损伤前交叉韧带和内侧副韧带成纤维细胞赖氨酰氧化酶和基质金属蛋白酶谱的影响。
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Immunogenicity of allogeneic mesenchymal stem cells.同种异体间充质干细胞的免疫原性。
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The immunomodulatory capacity of mesenchymal stem cells.间充质干细胞的免疫调节能力。
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Mesenchymal stem/stromal cells (MSCs): role as guardians of inflammation.间充质干细胞(MSCs):作为炎症守护者的角色。
Mol Ther. 2012 Jan;20(1):14-20. doi: 10.1038/mt.2011.211. Epub 2011 Oct 18.
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Combined effects of TNF-α, IL-1β, and HIF-1α on MMP-2 production in ACL fibroblasts under mechanical stretch: an in vitro study.TNF-α、IL-1β 和 HIF-1α 对机械拉伸下 ACL 成纤维细胞 MMP-2 产生的联合作用:一项体外研究。
J Orthop Res. 2011 Jul;29(7):1008-14. doi: 10.1002/jor.21349. Epub 2011 Feb 22.
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Mesenchymal stem cells: mechanisms of inflammation.间充质干细胞:炎症机制。
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Human gingiva-derived mesenchymal stem cells elicit polarization of m2 macrophages and enhance cutaneous wound healing.人牙龈间充质干细胞诱导 m2 巨噬细胞极化并增强皮肤伤口愈合。
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使用间充质干细胞增强内侧副韧带愈合:细胞反应和细胞因子谱的剂量效应。

Enhanced medial collateral ligament healing using mesenchymal stem cells: dosage effects on cellular response and cytokine profile.

机构信息

Department of Orthopedics and Rehabilitation, University of Wisconsin, 1111 Highland Ave., 5th Floor WIMR, Madison, WI, 53705, USA.

出版信息

Stem Cell Rev Rep. 2014 Feb;10(1):86-96. doi: 10.1007/s12015-013-9479-7.

DOI:10.1007/s12015-013-9479-7
PMID:24174129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3946728/
Abstract

Mesenchymal stem cells (MSCs) have potential therapeutic applications for musculoskeletal injuries due to their ability to differentiate into several tissue cell types and modulate immune and inflammatory responses. These immune-modulatory properties were examined in vivo during early stage rat medial collateral ligament healing. Two different cell doses (low dose 1 × 10(6) or high dose 4 × 10(6) MSCs) were administered at the time of injury and compared with normal ligament healing at days 5 and 14 post-injury. At both times, the high dose MSC group demonstrated a significant decrease in M2 macrophages compared to controls. At day 14, fewer M1 macrophages were detected in the low dose group compared to the high dose group. These results, along with significant changes in procollagen I, proliferating cells, and endothelialization suggest that MSCs can alter the cellular response during healing in a dose-dependent manner. The higher dose ligaments also had increased expression of several pro-inflammatory cytokines at day 5 (IL-1β, IFNγ, IL-2) and increased expression of IL-12 at day 14. Mechanical testing at day 14 revealed increased failure strength and stiffness in low dose ligaments compared to controls. Based on these improved mechanical properties, MSCs enhanced functional healing when applied at a lower dose. Different doses of MSCs uniquely affected the cellular response and cytokine expression in healing ligaments. Interestingly, the lower dose of cells proved to be most effective in improving functional properties.

摘要

间充质干细胞(MSCs)因其能够分化为多种组织细胞类型并调节免疫和炎症反应,因此在肌肉骨骼损伤方面具有潜在的治疗应用。这些免疫调节特性在早期大鼠内侧副韧带愈合过程中进行了体内研究。在损伤时给予两种不同的细胞剂量(低剂量 1×10(6)或高剂量 4×10(6)MSCs),并与损伤后 5 天和 14 天的正常韧带愈合进行比较。在这两个时间点,与对照组相比,高剂量 MSC 组的 M2 巨噬细胞数量明显减少。在第 14 天,低剂量组的 M1 巨噬细胞数量比高剂量组少。这些结果,以及前胶原 I、增殖细胞和内皮化的显著变化表明,MSCs 可以以剂量依赖的方式改变愈合过程中的细胞反应。在第 5 天(IL-1β、IFNγ、IL-2)和第 14 天(IL-12),高剂量韧带的几种促炎细胞因子表达也增加。第 14 天的力学测试显示,与对照组相比,低剂量韧带的失效强度和刚度增加。基于这些改善的机械性能,当以较低剂量应用时,MSCs 增强了功能愈合。不同剂量的 MSCs 独特地影响了愈合韧带中的细胞反应和细胞因子表达。有趣的是,较低剂量的细胞在改善功能特性方面最为有效。