Plasma-Based Scaffold Containing Bone-Marrow Mononuclear Cells Promotes Wound Healing in a Mouse Model of Pressure Injury.

IF 3.2 4区 医学 Q3 CELL & TISSUE ENGINEERING
Maria Alvarez-Viejo, Luis Romero-Rosal, Marcos Perez-Basterrechea, Jose M García-Gala, Pablo Hernando-Rodriguez, Jesus Marana-Gonzalez, Miriam Rubiera-Valdes, Blanca Vivanco-Allende, Angeles Fernandez-Rodriguez, Eva Martinez-Revuelta, Silvia Perez-Lopez
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引用次数: 0

Abstract

Pressure injuries, or pressure ulcers, are a common problem that may lead to infections and major complications, besides being a social and economic burden due to the costs of treatment and hospitalization. While surgery is sometimes necessary, this also has complications such as recurrence or wound dehiscence. Among the newer methods of pressure injury treatment, advanced therapies are an interesting option. This study examines the healing properties of bone marrow mononuclear cells (BM-MNCs) embedded in a plasma-based scaffold in a mouse model. Pressure ulcers were created on the backs of mice (2 per mouse) using magnets and assigned to a group of ulcers that were left untreated (Control, n = 15), treated with plasma scaffold (Plasma, n = 15), or treated with plasma scaffold containing BM-MNC (Plasma + BM-MNC, n = 15). Each group was examined at three time points (3, 7, and 14 days) after the onset of treatment. At each time point, animals were subjected to biometric assessment, bioluminescence imaging, and tomography. Once treatment had finished, skin biopsies were processed for histological and wound healing reverse transcription polymerase chain reaction (RT-PCR) array studies. While wound closure percentages were higher in the Plasma and Plasma + BM-MNC groups, differences were not significant, and thus descriptive data are provided. In all individuals, the presence of donor cells was revealed by immunohistochemistry on posttreatment onset Days 3, 7, and 14. In the Plasma + BM-MNC group, less inflammation was observed by positron emission tomography-computed tomography (PET/CT) imaging of the mice at 7 days, and a complete morphometabolic response was produced at 14 days, in accordance with histological results. A much more pronounced inflammatory process was observed in controls than in the other two groups, and this persisted until Day 14 after treatment onset. RT-PCR array gene expression patterns were also found to vary significantly, with the greatest difference noted between both treatments at 14 days when 11 genes were differentially expressed.

含骨髓单核细胞的血浆基支架促进压力损伤小鼠模型的伤口愈合
压伤或压疮是一种常见的问题,除了因治疗和住院费用而造成社会和经济负担外,还可能导致感染和重大并发症。虽然有时需要进行手术治疗,但也会出现复发或伤口开裂等并发症。在治疗压力性损伤的新方法中,先进疗法是一种有趣的选择。本研究在小鼠模型中研究了嵌入血浆基支架的骨髓单核细胞(BM-MNCs)的愈合特性。用磁铁在小鼠背上造成褥疮(每只小鼠 2 个),并将褥疮分为未处理组(对照组,n = 15)、用血浆支架处理组(血浆组,n = 15)或用含有骨髓单核细胞的血浆支架处理组(血浆 + 骨髓单核细胞组,n = 15)。每组在治疗开始后的三个时间点(3 天、7 天和 14 天)进行检查。在每个时间点,对动物进行生物计量评估、生物发光成像和断层扫描。治疗结束后,对皮肤活检进行组织学和伤口愈合反转录聚合酶链反应(RT-PCR)阵列研究。虽然血浆组和血浆 + BM-MNC 组的伤口闭合率较高,但差异并不显著,因此提供了描述性数据。在治疗后第 3、7 和 14 天,免疫组化显示所有患者体内都存在供体细胞。在血浆 + BM-MNC 组,小鼠在 7 天时的正电子发射断层扫描(PET/CT)成像观察到的炎症较少,14 天时产生了完全的形态代谢反应,与组织学结果一致。对照组的炎症过程比其他两组明显得多,这种情况一直持续到治疗开始后的第 14 天。RT-PCR 阵列基因表达模式也有显著差异,两种治疗方法在 14 天时差异最大,有 11 个基因表达不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Transplantation
Cell Transplantation 生物-细胞与组织工程
CiteScore
6.00
自引率
3.00%
发文量
97
审稿时长
6 months
期刊介绍: Cell Transplantation, The Regenerative Medicine Journal is an open access, peer reviewed journal that is published 12 times annually. Cell Transplantation is a multi-disciplinary forum for publication of articles on cell transplantation and its applications to human diseases. Articles focus on a myriad of topics including the physiological, medical, pre-clinical, tissue engineering, stem cell, and device-oriented aspects of the nervous, endocrine, cardiovascular, and endothelial systems, as well as genetically engineered cells. Cell Transplantation also reports on relevant technological advances, clinical studies, and regulatory considerations related to the implantation of cells into the body in order to provide complete coverage of the field.
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