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使用无光毒性蓝光增强条件培养基的血管生成功效以促进伤口愈合。

Fortifying angiogenic efficacy of conditioned media using phototoxic-free blue light for wound healing.

作者信息

Kim Sung-Won, Im Gwang-Bum, Kim Yeong Hwan, Bhang Suk Ho

机构信息

School of Chemical Engineering, Sungkyunkwan University Suwon South Korea.

Present address: Department of Cardiac Surgery Boston Children's Hospital and Harvard Medical School Boston Massachusetts USA.

出版信息

Bioeng Transl Med. 2022 Dec 8;8(3):e10462. doi: 10.1002/btm2.10462. eCollection 2023 May.

DOI:10.1002/btm2.10462
PMID:37206233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10189464/
Abstract

We used a blue organic light-emitting diode (bOLED) to increase the paracrine factors secreted from human adipose-derived stem cells (hADSCs) for producing conditioned medium (CM). Our results showed that while the bOLED irradiation promotes a mild-dose reactive oxygen generation that enhances the angiogenic paracrine secretion of hADSCs, it does not induce phototoxicity. The bOLED enhances paracrine factors via a cell-signaling mechanism involving hypoxia-inducible factor 1 alpha. This study demonstrated that the CM resulting from bOLED treatment shows improved therapeutic effects on mouse wound-healing models. This method contributes to overcoming the barriers to stem-cell therapies, including the toxicity and low yields from other methods such as nanoparticles, synthetic polymers, and even cell-derived vesicles.

摘要

我们使用蓝色有机发光二极管(bOLED)来增加人脂肪来源干细胞(hADSCs)分泌的旁分泌因子,以制备条件培养基(CM)。我们的结果表明,虽然bOLED照射会促进适度剂量的活性氧生成,从而增强hADSCs的血管生成旁分泌分泌,但它不会诱导光毒性。bOLED通过涉及缺氧诱导因子1α的细胞信号传导机制增强旁分泌因子。这项研究表明,bOLED处理产生的CM对小鼠伤口愈合模型具有更好的治疗效果。这种方法有助于克服干细胞疗法的障碍,包括纳米颗粒、合成聚合物甚至细胞衍生囊泡等其他方法的毒性和低产量问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/6eae6ec0c09b/BTM2-8-e10462-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/192f00519d71/BTM2-8-e10462-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/8b9f23eac802/BTM2-8-e10462-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/59788e648658/BTM2-8-e10462-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/fc5d84122a6b/BTM2-8-e10462-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/6eae6ec0c09b/BTM2-8-e10462-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/192f00519d71/BTM2-8-e10462-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/8b9f23eac802/BTM2-8-e10462-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/59788e648658/BTM2-8-e10462-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/fc5d84122a6b/BTM2-8-e10462-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c0/10189464/6eae6ec0c09b/BTM2-8-e10462-g004.jpg

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