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研究 2D 和 3D 培养条件对人骨髓间充质干细胞分泌组体外和体内角膜伤口愈合治疗效果的影响。

Characterizing the impact of 2D and 3D culture conditions on the therapeutic effects of human mesenchymal stem cell secretome on corneal wound healing in vitro and ex vivo.

机构信息

Ophthalmology, Byers Eye Institute at Stanford University School of Medicine, Palo Alto, CA, United States.

Ophthalmology, Byers Eye Institute at Stanford University School of Medicine, Palo Alto, CA, United States; Chemical and Biological Engineering, Gachon University, Seongnam-si, Gyeonggi-do, Republic of Korea.

出版信息

Acta Biomater. 2019 Nov;99:247-257. doi: 10.1016/j.actbio.2019.09.022. Epub 2019 Sep 17.

Abstract

The therapeutic effects of secreted factors (secretome) produced by bone marrow-derived human mesenchymal stem cells (MSCs) were evaluated as a function of their growth in 2D culture conditions and on 3D electrospun fiber scaffolds. Electrospun fiber scaffolds composed of polycaprolactone and gelatin were fabricated to provide a 3D microenvironment for MSCs, and their mechanical properties were optimized to be similar to corneal tissue. The secretome produced by the MSCs cultured on 3D fiber matrices versus 2D culture dishes were analyzed using a Luminex immunoassay, and the secretome of MSCs cultured on the 3D versus 2D substrates showed substantial compositional differences. Concentrations of factors such as HGF and ICAM-1 were increased over 5 times in 3D cultures compared to 2D cultures. In vitro proliferation and scratch-based wound healing assays were performed to compare the effects of the secretome on corneal fibroblast cells (CFCs) when delivered synchronously from co-cultured MSCs through a trans-well co-culture system versus asynchronously after harvesting the factors separately and adding them to the media. Cell viability of CFCs was sustained for 6 days when co-cultured with MSCs seeded on the fibers but decreased with time under other conditions. Scratch assays showed 95% closure at 48 h when CFCs were co-cultured with MSCs seeded on fibers, while the control group only exhibited 50% closure at 48 h. Electrospun fibers seeded with MSCs were then applied to a rabbit corneal organ culture system, and MSCs seeded on fibers promoted faster epithelialization and less scarring. Corneas were fixed and stained for alpha smooth muscle actin (α-SMA), and then analyzed by confocal microscopy. Immunostaining showed that expression of α-SMA was lower in corneas treated with MSCs seeded on fibers, suggesting suppression of myofibroblastic transformation. MSCs cultured on electrospun fibers facilitate wound healing in CFCs and on explanted corneas through differential secretome profiles compared to MSCs cultured on 2D substrates. Future work is merited to further understand the nature and basis of these differences and their effects in animal models. STATEMENT OF SIGNIFICANCE: Previous studies have shown that the secretome of bone marrow-derived mesenchymal stem cells (MSC) is promotes corneal wound healing by facilitating improved wound closure rates and reduction of scarring and neovascularization. The present research is significant because it provides evidence for the modulation of the secretome as a function of the MSC culture environment. This leads to differential expression of therapeutic factors secreted, which can impact corneal epithelial and stromal healing after severe injury. In addition, this article shows that co-continuous delivery of the MSC secretome improves cell migration and proliferation over aliquoted delivery, and that MSCs grown on three-dimensional electrospun fiber constructs may provide a favorable microenvironment for cultured MSCs and as a carrier to deliver their secreted factors to the ocular surface.

摘要

研究了骨髓间充质干细胞(MSC)分泌因子(分泌组)的治疗效果,这些因子的产生取决于它们在二维培养条件和三维静电纺纤维支架上的生长情况。制备了由聚己内酯和明胶组成的静电纺纤维支架,为 MSC 提供 3D 微环境,并对其机械性能进行了优化,使其与角膜组织相似。使用 Luminex 免疫测定法分析了在 3D 纤维基质上培养的 MSC 与在 2D 培养皿上培养的 MSC 的分泌组,结果显示,在 3D 培养物中,HGF 和 ICAM-1 等因子的浓度比 2D 培养物高 5 倍以上。体外增殖和划痕愈合试验比较了在共培养系统中同步从共培养的 MSC 传递分泌因子与分别收获因子并添加到培养基中异步传递分泌因子对角膜成纤维细胞(CFC)的影响。当与纤维上接种的 MSC 共培养时,CFC 的细胞活力可维持 6 天,但在其他条件下随时间推移而降低。划痕试验显示,当 CFC 与纤维上接种的 MSC 共培养时,48 小时时 95%的划痕闭合,而对照组仅在 48 小时时闭合 50%。然后将纤维上接种的 MSC 应用于兔角膜器官培养系统,纤维上接种的 MSC 促进更快的上皮化和更少的瘢痕形成。固定和染色角膜用于α平滑肌肌动蛋白(α-SMA),然后通过共聚焦显微镜进行分析。免疫染色显示,纤维上接种的 MSC 处理的角膜中 α-SMA 的表达较低,提示肌成纤维转化受到抑制。与在 2D 基质上培养的 MSC 相比,在静电纺纤维上培养的 MSC 通过差异分泌组谱促进 CFC 中的伤口愈合和在离体角膜上的伤口愈合。值得进一步研究以更好地了解这些差异的性质和基础及其在动物模型中的作用。意义:先前的研究表明,骨髓间充质干细胞(MSC)的分泌组通过促进伤口闭合率的提高以及减少瘢痕形成和新生血管化来促进角膜伤口愈合。本研究具有重要意义,因为它提供了证据表明 MSC 培养环境是作为调节分泌组的因素。这导致了治疗因子分泌的差异表达,这可能会影响严重损伤后的角膜上皮和基质愈合。此外,本文表明,MSC 分泌组的连续共递送比分批递送更能促进细胞迁移和增殖,并且在三维静电纺纤维构建体上生长的 MSC 可为培养的 MSC 提供有利的微环境,并作为载体将其分泌因子递送至眼表面。

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