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增强肌腱再生:研究拓扑结构对脂肪来源干细胞分泌组的影响。

Enhancing Tendon Regeneration: Investigating the Impact of Topography on the Secretome of Adipose-Derived Stem Cells.

作者信息

Long Qiuzi, Liu Chuanquan, Zheng Haotian, Wang Mingyue, Liu Hanmei, Liu Yue, Cao Zhicheng, Sun Yuzhi, Mo Qingyun, Backman Ludvig J, Zhu Jialin, Hu Lizhi, Huang Jinlong, Zhang Wei, Chen Jialin

机构信息

Nanjing University of Chinese Medicine, Nanjing, 210029, China.

Center for Stem Cell and Regenerative Medicine, Southeast University, Nanjing, 210009, China.

出版信息

Adv Sci (Weinh). 2025 May;12(18):e2417447. doi: 10.1002/advs.202417447. Epub 2025 Mar 17.


DOI:10.1002/advs.202417447
PMID:40091553
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12079404/
Abstract

Tendons are vital for maintaining integrity and movement, but current treatment options are insufficient for their regeneration after injuries. Previous studies have shown that the secretome from mesenchymal stem cells (MSCs) promoted tendon regeneration. However, limited studies have explored the impact of the physical microenvironment on the secretome's efficacy of MSCs. In this study, it is shown that the topographic orientation regulates the secretome of human adipose-derived stem cells (ADSCs) and promotes tendon regeneration. Conditioned medium (CM) is collected from ADSCs cultured on the scaffolds with different topography. The results show that CM generated from aligned structure group has a potent effect in promoting cell migration and proliferation, tenogenic differentiation, macrophage polarization toward M2 phenotype, tendon structure and mechanical function recovery. Proteomic analysis revealed that the aligned structure can up-regulate the secretion of Extracellular matrix (ECM) proteins while down-regulate proinflammatory factors. This modulation activates the MAPK, GPCR and Integrin signaling pathways which may account for the enhanced effect on tendon regeneration. This study offers a promising and safer non-cell-based treatment option for tendon repair.

摘要

肌腱对于维持完整性和运动至关重要,但目前的治疗方法在肌腱损伤后的再生方面并不充分。先前的研究表明,间充质干细胞(MSCs)的分泌组可促进肌腱再生。然而,关于物理微环境对MSCs分泌组功效影响的研究较少。在本研究中,表明拓扑取向可调节人脂肪来源干细胞(ADSCs)的分泌组并促进肌腱再生。条件培养基(CM)取自培养于具有不同拓扑结构支架上的ADSCs。结果表明,由排列结构组产生的CM在促进细胞迁移和增殖、肌腱分化、巨噬细胞向M2表型极化、肌腱结构和力学功能恢复方面具有显著作用。蛋白质组学分析显示,排列结构可上调细胞外基质(ECM)蛋白的分泌,同时下调促炎因子。这种调节激活了MAPK、GPCR和整合素信号通路,这可能解释了对肌腱再生增强的作用。本研究为肌腱修复提供了一种有前景且更安全的非细胞治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/893e57ba4076/ADVS-12-2417447-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/eef46a13bf0b/ADVS-12-2417447-g012.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/9d4ea5ccc04c/ADVS-12-2417447-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/009439242fdf/ADVS-12-2417447-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/f233569e830e/ADVS-12-2417447-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/87e34ce50a54/ADVS-12-2417447-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/a5d1e1eb9a92/ADVS-12-2417447-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/40138c8152c7/ADVS-12-2417447-g009.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/893e57ba4076/ADVS-12-2417447-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/eef46a13bf0b/ADVS-12-2417447-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/e3a252f34f19/ADVS-12-2417447-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/9d4ea5ccc04c/ADVS-12-2417447-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/009439242fdf/ADVS-12-2417447-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/f233569e830e/ADVS-12-2417447-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/87e34ce50a54/ADVS-12-2417447-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/a5d1e1eb9a92/ADVS-12-2417447-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/40138c8152c7/ADVS-12-2417447-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/50ea6e396741/ADVS-12-2417447-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/ff46f4649ffa/ADVS-12-2417447-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064c/12079404/893e57ba4076/ADVS-12-2417447-g008.jpg

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本文引用的文献

[1]
Effects of adipose-derived mesenchymal stem cell conditioned medium on human tenocytes exposed to high glucose.

Ther Adv Musculoskelet Dis. 2024-1-8

[2]
Complement factor H attenuates TNF-α-induced inflammation by upregulating EIF3C in rheumatoid arthritis.

J Transl Med. 2023-11-23

[3]
Decellularization-Based Modification Strategy for Bioactive Xenografts Promoting Tendon Repair.

Adv Healthc Mater. 2024-2

[4]
Synovium-Derived Mesenchymal Stem Cell-Based Scaffold-Free Fibrocartilage Engineering for Bone-Tendon Interface Healing in an Anterior Cruciate Ligament Reconstruction Model.

Tissue Eng Regen Med. 2024-2

[5]
Cell-autonomous regulation of complement C3 by factor H limits macrophage efferocytosis and exacerbates atherosclerosis.

Immunity. 2023-8-8

[6]
An Update on Adipose-Derived Stem Cells for Regenerative Medicine: Where Challenge Meets Opportunity.

Adv Sci (Weinh). 2023-7

[7]
Mesenchymal stromal/stem cell (MSC)-derived exosomes in clinical trials.

Stem Cell Res Ther. 2023-4-7

[8]
Biomimetic natural biomaterials for tissue engineering and regenerative medicine: new biosynthesis methods, recent advances, and emerging applications.

Mil Med Res. 2023-3-28

[9]
Caveolin-1 is involved in fatty infiltration and bone-tendon healing of rotator cuff tear.

Mol Med. 2023-3-14

[10]
Targeting integrin pathways: mechanisms and advances in therapy.

Signal Transduct Target Ther. 2023-1-2

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