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机械处理脂肪组织在骨关节炎治疗中的潜在体外再生特性展望。

Prospects on the Potential In Vitro Regenerative Features of Mechanically Treated-Adipose Tissue for Osteoarthritis Care.

机构信息

Laboratorio RAMSES, IRCCS Istituto Ortopedico Rizzoli, Bologna, 40136, Italy.

Laboratorio di ImmunoReumatologia e Rigenerazione Tissutale, IRCCS Istituto Ortopedico Rizzoli, Bologna, 40136, Italia.

出版信息

Stem Cell Rev Rep. 2021 Aug;17(4):1362-1373. doi: 10.1007/s12015-020-10099-2. Epub 2021 Jan 19.

DOI:10.1007/s12015-020-10099-2
PMID:33469783
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8316247/
Abstract

Gathering a better grasp on the adipose stromal vascular fraction (SVF) is demanding among clinicians for osteoarthritis (OA) care because of its promising but multifaceted clinical outcomes. The aim of this preclinical in vitro study was to test whether the mechanical approach with Hy-Tissue SVF system, a class IIa CE marked device of adipose tissue micro-fragmentation, influences the biological features and functions of SVF. We compared mechanical generated-SVF (mSVF) with the enzymatic generated-SVF (eSVF) by testing cell survival, phenotype, differentiation, and paracrine properties using ELISA assays. Both adipose SVF showed 80% viable cells and enrichment for CD-44 marker. The mSVF product preserved the functions of cell populations within the adipose tissue; however, it displayed lowered nucleated cell recovery and CFU-F than eSVF. As for multipotency, mSVF and eSVF showed similar differentiation commitment for osteochondral lineages. Both adipose SVF exhibited an increased release of VEGF, HGF, IGF-1 and PDGF-bb, involved in pathways mediating osteochondral repair and cell migration. Both mSVF and eSVF also displayed high release for the anti-inflammatory cytokine IL-10. After in vitro culture, supernatants from both mSVF and eSVF groups showed a low release of cytokines except for IL-10, thereby giving evidence of functional changes after culture expansion. In this study, mSVF showed active cell populations in the adipose tissue comparable to eSVF with excellent survival, differentiation and paracrine properties under a new mechanical adipose tissue micro-fragmentation system; thereby suggesting its potential use as a minimally invasive technique for OA treatment.

摘要

临床医生在骨关节炎(OA)治疗中需要更好地了解脂肪基质血管部分(SVF),因为其具有有前途但多方面的临床结果。本临床前体外研究的目的是测试使用 Hy-Tissue SVF 系统进行机械方法(一种 IIa 类 CE 标记的脂肪组织微碎片设备)是否会影响 SVF 的生物学特征和功能。我们通过使用 ELISA 测定来测试细胞存活,表型,分化和旁分泌特性,比较了机械产生的-SVF(mSVF)与酶产生的-SVF(eSVF)。两种脂肪 SVF 均显示出 80%的活细胞和 CD-44 标志物的富集。mSVF 产品保留了脂肪组织内细胞群体的功能;但是,与 eSVF 相比,其核细胞回收和 CFU-F 降低。就多能性而言,mSVF 和 eSVF 显示出相似的成骨软骨谱系分化承诺。两种脂肪 SVF 均表现出参与介导骨软骨修复和细胞迁移的途径中 VEGF、HGF、IGF-1 和 PDGF-bb 的释放增加。mSVF 和 eSVF 也表现出抗炎细胞因子 IL-10 的高释放。体外培养后,mSVF 和 eSVF 两组的上清液均显示出除 IL-10 以外的细胞因子低释放,从而证明培养扩增后存在功能变化。在这项研究中,mSVF 显示出与 eSVF 相当的脂肪组织中的活性细胞群体,具有出色的生存能力,分化能力和旁分泌特性,在新型机械脂肪组织微碎片系统下;因此,建议将其作为一种微创技术用于 OA 治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/21b5b311cc23/12015_2020_10099_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/109ffc65310e/12015_2020_10099_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/19214a58eb3d/12015_2020_10099_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/a84756cc788f/12015_2020_10099_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/e2c8306271f0/12015_2020_10099_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/4da9889e1177/12015_2020_10099_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/21b5b311cc23/12015_2020_10099_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/109ffc65310e/12015_2020_10099_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/19214a58eb3d/12015_2020_10099_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/a84756cc788f/12015_2020_10099_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/e2c8306271f0/12015_2020_10099_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/4da9889e1177/12015_2020_10099_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ffa/8316247/21b5b311cc23/12015_2020_10099_Fig6_HTML.jpg

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