间充质干细胞衍生的外泌体增强羊膜提取物促进角膜角质细胞增殖

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biotechnology Progress Pub Date : 2024-04-11 DOI:10.1002/btpr.3465
Fatma Zehra Erkoc-Biradli, Berkay Erenay, Alp Ozgun, Hayriye Öztatlı, Ferda Işık, Utku Ateş, Rıfat Rasier, Bora Garipcan
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引用次数: 0

摘要

羊膜提取物(AME)和Wharton's jelly间充质干细胞衍生外泌体(WJ-MSC-Exos)是很有前景的治疗方案,它们在组织工程和再生医学,特别是皮肤和角膜伤口愈合应用方面的潜力已得到探索。AME 是人类羊膜的一种提取物,已知含有大量细胞因子和生长因子,因此在局部应用方面极具吸引力。同样,WJ-间充质干细胞提取物也因其伤口愈合特性而备受关注。虽然 WJ-间充质干细胞-Exos 和 AME 已被分别用于伤口愈合研究,但它们的联合协同效应尚未得到广泛研究。在这项研究中,我们评估了 AME 和 WJ-MSC-Exos 单独或联合使用对角膜角质细胞增殖的影响,以及它们促进体外细胞迁移、伤口愈合的能力和对细胞形态的影响。我们的研究结果表明,外泌体(3 × 105 Exo/mL)和AME(50 μg/mL)可协同促进角膜角质细胞的增殖。与第 3 天仅使用 50 μg/mL AME 处理相比,联合使用这些溶液(3 × 105 Exo/mL + 50 μg/mL)可增加细胞增殖(**** p <0.0001)。这种混合处理(3 × 105 Exo/mL + 50 μg/mL)与单独的 WJ-MSC-Exo 处理(3 × 105 Exo/mL)相比,提高了伤口闭合率(*p < 0.05)。总之,角膜角质细胞经AME和WJ-间充质干细胞-Exo(3 × 105 Exo/mL + 50 μg/mL)混合物处理后,其增殖和伤口愈合趋势均有所增强。联合使用AME和WJ-间充质干细胞-Exo可为角膜修复研究奠定良好的基础。
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Mesenchymal stem cells derived-exosomes enhanced amniotic membrane extract promotes corneal keratocyte proliferation

Amniotic membrane extract (AME) and Wharton's jelly mesenchymal stem cells derived-exosomes (WJ-MSC-Exos) are promising therapeutic solutions explored for their potential in tissue engineering and regenerative medicine, particularly in skin and corneal wound healing applications. AME is an extract form of human amniotic membrane and known to contain a plethora of cytokines and growth factors, making it a highly attractive option for topical applications. Similarly, WJ-MSC-Exos have garnered significant interest for their wound healing properties. Although WJ-MSC-Exos and AME have been used separately for wound healing research, their combined synergistic effects have not been studied extensively. In this study, we evaluated the effects of both AME and WJ-MSC-Exos, individually and together, on the proliferation of corneal keratocytes as well as their ability to promote in vitro cell migration, wound healing, and their impact on cellular morphology. Our findings indicated that the presence of both exosomes (3 × 105 Exo/mL) and AME (50 μg/mL) synergistically enhance the proliferation of corneal keratocytes. Combined use of these solutions (3 × 105 Exo/mL + 50 μg/mL) increased cell proliferation compared to only 50 μg/mL AME treatment on day 3 (**** p < 0.0001). This mixture treatment (3 × 105 Exo/mL + 50 μg/mL) increased wound closure rate compared to isolated WJ-MSC-Exo treatment (3 × 105 Exo/mL) (*p < 0.05). Overall, corneal keratocytes treated with AME and WJ-MSC-Exo (3 × 105 Exo/mL + 50 μg/mL) mixture resulted in enhanced proliferation and wound healing tendency. Utilization of combined use of AME and WJ-MSC-Exo can pave the way for a promising foundation for corneal repair research.

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来源期刊
Biotechnology Progress
Biotechnology Progress 工程技术-生物工程与应用微生物
CiteScore
6.50
自引率
3.40%
发文量
83
审稿时长
4 months
期刊介绍: Biotechnology Progress , an official, bimonthly publication of the American Institute of Chemical Engineers and its technological community, the Society for Biological Engineering, features peer-reviewed research articles, reviews, and descriptions of emerging techniques for the development and design of new processes, products, and devices for the biotechnology, biopharmaceutical and bioprocess industries. Widespread interest includes application of biological and engineering principles in fields such as applied cellular physiology and metabolic engineering, biocatalysis and bioreactor design, bioseparations and downstream processing, cell culture and tissue engineering, biosensors and process control, bioinformatics and systems biology, biomaterials and artificial organs, stem cell biology and genetics, and plant biology and food science. Manuscripts concerning the design of related processes, products, or devices are also encouraged. Four types of manuscripts are printed in the Journal: Research Papers, Topical or Review Papers, Letters to the Editor, and R & D Notes.
期刊最新文献
Non-thermal plasma decontamination of microbes: a state of the art. Mechanistic model of minute virus of mice elution behavior in anion exchange chromatography purification. Comparing in silico flowsheet optimization strategies in biopharmaceutical downstream processes. General strategies for IgG-like bispecific antibody purification. Issue Information
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