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人血小板衍生外泌体产品给药后对体外神经突生长的剂量反应分析。

Dose-response analysis after administration of a human platelet-derived exosome product on neurite outgrowth in vitro.

作者信息

Saffari Sara, Rademakers Daan J, Pulos Nicholas, Shin Alexander Y

机构信息

Department of Orthopedic Surgery, Division of Hand and Microvascular Surgery, Mayo Clinic, Rochester, Minnesota, USA.

Department of Plastic Surgery, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, The Netherlands.

出版信息

Biotechnol Bioeng. 2023 Nov;120(11):3191-3199. doi: 10.1002/bit.28520. Epub 2023 Aug 4.

Abstract

Modulating the nerve's local microenvironment using exosomes is proposed to enhance nerve regeneration. This study aimed to determine the optimal dose of purified exosome product (PEP) required to exert maximal neurite extension. An in vitro dorsal root ganglion (DRG) neurite outgrowth assay was used to evaluate the effect of treatment with (i) 5% PEP, (ii) 10% PEP, (iii) 15% PEP, or (iv) 20% PEP on neurite extension (N = 9/group), compared to untreated controls. After 72 h, neurite extension was measured to quantify nerve regeneration. Live cell imaging was used to visualize neurite outgrowth during incubation. Treatment with 5% PEP resulted in the longest neurite extension and was superior to the untreated DRG (p = 0.003). Treatment with 10% PEP, 15% PEP, and 20% PEP was found to be comparable to controls (p = 0.12, p = 0.06, and p = 0.41, respectively) and each other. Live cell imaging suggested that PEP migrated towards the DRG neural regeneration site, compared to the persistent homogenous distribution of PEP in culture media alone. 5% PEP was found to be the optimal concentration for nerve regeneration based on this in vitro dose-response analysis.

摘要

有人提出利用外泌体调节神经的局部微环境以促进神经再生。本研究旨在确定发挥最大神经突延伸所需的纯化外泌体产品(PEP)的最佳剂量。使用体外背根神经节(DRG)神经突生长试验来评估用(i)5% PEP、(ii)10% PEP、(iii)15% PEP或(iv)20% PEP处理对神经突延伸的影响(每组N = 9),并与未处理的对照组进行比较。72小时后,测量神经突延伸以量化神经再生。使用活细胞成像观察孵育过程中的神经突生长。用5% PEP处理导致最长的神经突延伸,且优于未处理的DRG(p = 0.003)。发现用10% PEP、15% PEP和20% PEP处理与对照组相当(分别为p = 0.12、p = 0.06和p = 0.41),且它们之间也相当。活细胞成像表明,与单独培养基中PEP持续均匀分布相比,PEP向DRG神经再生部位迁移。基于此体外剂量反应分析,发现5% PEP是神经再生的最佳浓度。

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