脐带(UC)血清、人血小板裂解液以及纳米姜黄素和藏红花素对人脐带间充质基质细胞(MSCs)增殖和存活的协同作用

IF 2.2
Akram Sheikh, Javad Baharara, Najmeh Kaffash Farkhad, Mahmoud Reza Jafari, Mohammad Amin Kerachian, Jalil Tavakol Afshari
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引用次数: 0

摘要

胎牛血清(FBS)是间充质基质细胞(MSC)培养的常规补充物,存在伦理问题、批次差异和病原体传播风险。本研究旨在评估人源性脐带血清(UCS)和人血小板裂解液(HPL)作为FBS的无xeno替代品,并评估纳米姜黄素和藏红花素作为补充剂对人脐带源性间充质干细胞增殖和存活的协同作用。方法:人脐带来源的MSCs在添加10%胎牛血清(对照)、UCS或HPL的培养基中培养。分别用纳米姜黄素(0.3 μM)或藏红花素(2.5 μM)单独或联合处理。MTT法检测细胞增殖,Annexin V/PI流式细胞术检测细胞凋亡,RT-qPCR法检测多能基因(Sox2、Nanog、Oct4)表达。结果:与FBS对照组相比,UCS和HPL补充剂显著增加了MSC增殖(p < 0.001)。具体来说,UCS减少了大约50%的人口倍增时间。添加藏红花素可减少高达30%的细胞凋亡(p = 0.04),并显著提高多能基因Sox2和Nanog的表达,特别是在添加HPL的培养中。相比之下,在所有测试条件下,纳米姜黄素抑制MSC增殖并增加凋亡。讨论:结果表明,UCS和HPL是FBS有效、可行的替代方案,可促进MSC的卓越扩展。藏红花素的抗凋亡和增强干细胞的特性突出了其作为提高培养质量和细胞存活率的有价值的添加剂的潜力。纳米姜黄素观察到的细胞毒性作用强调了对剂量优化研究的迫切需要。本研究的主要局限性是补充剂使用了固定浓度,这需要进一步研究不同剂量的补充剂。结论:UCS和HPL是MSC生物制造中FBS的可靠的、合乎伦理的替代品。藏红花素可以通过提高细胞存活率和维持干细胞特性来进一步提高培养效果。这些发现支持了优化的、无异种培养系统的发展,用于可扩展的MSC生产,这对于推进再生医学治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Efficacy of Umbilical Cord (UC) Serum, Human Platelet Lysate, and the Synergistic Effect of Nano-curcumin and Crocin as Supplements in the Proliferation and Survival of Human UC-derived Mesenchymal Stromal Cells (MSCs).

Introduction: Fetal Bovine Serum (FBS), the conventional supplement for Mesenchymal Stromal Cell (MSC) culture, presents ethical issues, batch variability, and risks of pathogen transmission. This study aimed to evaluate human-derived Umbilical Cord Serum (UCS) and Human Platelet Lysate (HPL) as xeno-free alternatives to FBS and to assess the synergistic effects of nano-curcumin and crocin as supplements to enhance the proliferation and survival of human umbilical cord-derived MSCs.

Methods: Human umbilical cord-derived MSCs were cultured in media supplemented with 10% FBS (control), UCS, or HPL. These groups were further treated with nano-curcumin (0.3 μM) or crocin (2.5 μM), either individually or in combination. Cell proliferation was measured using the MTT assay, apoptosis was assessed by Annexin V/PI flow cytometry, and pluripotency gene expression (Sox2, Nanog, Oct4) was analyzed by RT-qPCR.

Results: UCS and HPL supplements significantly increased MSC proliferation compared to the FBS control (p < 0.001). Specifically, UCS reduced the population doubling time by approximately 50%. Supplementation with crocin reduced apoptosis by up to 30% (p = 0.04) and significantly enhanced the expression of the pluripotency genes Sox2 and Nanog, particularly in cultures supplemented with HPL. In contrast, nano-curcumin inhibited MSC proliferation and increased apoptosis across all tested conditions.

Discussions: The results demonstrate that UCS and HPL are effective, viable alternatives to FBS, promoting superior MSC expansion. The anti-apoptotic and stemness-enhancing properties of crocin highlight its potential as a valuable additive for improving culture quality and cell survival. The cytotoxic effects observed with nano-curcumin underscore a critical need for dose-optimization studies. The primary limitation of this study is the use of fixed concentrations for the supplements, which warrants further investigation across a range of doses.

Conclusion: UCS and HPL are robust, ethically sound replacements for FBS in MSC biomanufacturing. Crocin can further enhance culture outcomes by improving cell survival and maintaining stem cell properties. These findings support the development of optimized, xeno-free culture systems for scalable MSC production, which is crucial for advancing regenerative medicine therapies.

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