基于人类沃顿果冻间充质干细胞分泌组的局部凝胶的治疗应用潜力。

Q3 Biochemistry, Genetics and Molecular Biology Avicenna journal of medical biotechnology Pub Date : 2024-10-01 DOI:10.18502/ajmb.v16i4.16739
Wahyu Widowati, Ahmad Faried, Rimonta Febby Gunanegara, Fanny Rahardja, Fadhilah Haifa Zahiroh, Annisa Firdaus Sutendi, Faradhina Salfa Nindya, Rizal Azis, Renandy Kristianlie Ekajaya
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引用次数: 0

摘要

背景:糖尿病足溃疡(DFU)可能会因神经病变和血管问题而恶化。这种疾病可导致 14.3% 的患者死亡,因此需要有效的伤口愈合疗法。伤口愈合是一个复杂的生物过程,而人类沃顿果冻间充质干细胞(hWJMSCs)可能有助于控制糖尿病足溃疡的治疗问题。本研究的重点是利用凝胶载体从沃顿果冻间充质干细胞分泌组(hWJ-MSCs-Sec)中输送生物活性物质,作为治疗 DFU 的一种可能方法:为保证质量,hWJ-MSCs-Sec与卡波姆凝胶充分混合并冷冻干燥。方法:将 hWJMSCs-Sec 与卡波姆凝胶充分混合并冷冻干燥,然后进行 ELISA 检测,以确定 hWJMSCs-Sec 凝胶的特性,如角质细胞生长因子(KGF)、血小板衍生生长因子(PDGF)、肝细胞生长因子(HGF)、表皮生长因子(EGF)和肝素结合型 EGF 样生长因子(HB-EGF)。抗氧化活性还通过过氧化氢(H2O2)、一氧化氮(NO)和铁还原抗氧化力(FRAP)测定法进行了测定。使用 WST-8 进行增殖试验,并通过划痕人皮肤成纤维细胞(BJ 细胞)的迁移能力评估伤口愈合潜力:结果:与新鲜的hWJ-MSCs-Sec相比,冻干的hWJ-MSCs-Sec显示出更高水平的KGF、HGF、PDGF、EGF、HB-EGF和抗氧化活性。此外,与新鲜 hWJ-MSCs-Sec 的凝胶相比,冻干 hWJ-MSCs-Sec 的凝胶表现出更高的水平。用 hWJMSCs-Sec 和冻干 hWJ-MSCs-Sec 凝胶处理的 BJ 细胞上划伤的伤口闭合得更快,就证明了这一点:结论:冻干hWJ-MSCs-Sec凝胶的质量优于非冻干hWJ-MSCs-Sec凝胶。这表明冷冻干燥过程可以保持 hWJ-间充质干细胞-Sec 中的生物活性化学物质,从而有可能提高这种凝胶在促进伤口愈合的细胞再生方面的功效。
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The Potential of Human Wharton's Jelly Mesenchymal Stem Cells Secretome Based Topical Gel for Therapeutic Application.

Background: Diabetic Foot Ulcer (DFU) might be worsened by neuropathy and vascular issues. This condition can cause 14.3% fatality, stressing the need for effective wound healing therapy. Wound healing is a complex biological process, and human Wharton's Jelly Mesenchymal Stem Cells (hWJMSCs) may help manage DFU treatment issues. This research focuses on utilizing a gel carrier to deliver bioactive substances from Wharton's Jelly Mesenchymal Stem Cells secretome (hWJ-MSCs-Sec) as a possible treatment for DFU.

Methods: To maintain quality, hWJMSCs-Sec is thoroughly mixed with carbomer gel and freeze-dried. ELISA test is performed to determine the characterization of the gel of hWJMSCs-Sec such as Keratinocyte Growth Factor (KGF), Platelet-Derived Growth Factor (PDGF), Hepatocyte Growth Factor (HGF), Epidermal Growth Factor (EGF), and Heparin-Binding EGF-Like Growth Factor (HB-EGF). The antioxidant activity was also measured with Hydrogen peroxide (H2O2), Nitric oxide (NO), and Ferric Reducing Antioxidant Power (FRAP) assay. Proliferation assay was utilized using WST-8 and the wound healing potential was assessed via the migration cell ability of scratched-human skin fibroblast (BJ cells).

Results: The freeze-dried hWJ-MSCs-Sec showed higher levels of KGF, HGF, PDGF, EGF, HB-EGF, and the antioxidant activities compared to fresh hWJ-MSCs-Sec. Additionally, the gel of freeze-dried hWJ-MSCs-Sec exhibited higher levels compared to the gel of fresh hWJMSCs-Sec. This was evidenced by faster closure of scratched wounds on BJ cells treated with hWJMSCs-Sec and freeze-dried hWJ-MSCs-Sec gel.

Conclusion: The freeze-dried hWJ-MSCs-Sec gel exhibits superior quality compared to the non-freeze-dried hWJ-MSCs-Sec gel. This demonstrates that the freeze-drying procedure can maintain the bioactive chemicals found in hWJMSCs-Sec, potentially enhancing the efficacy of this gel in promoting cell regeneration for wound healing.

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来源期刊
Avicenna journal of medical biotechnology
Avicenna journal of medical biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
2.90
自引率
0.00%
发文量
43
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