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基于乙醛脱氢酶活性的骨髓间充质基质细胞亚群的分离和鉴定。

Isolation and Characterization of Bone Marrow Mesenchymal Stromal Cell Subsets in Culture Based on Aldehyde Dehydrogenase Activity.

机构信息

1 Department of Haematology, Laboratory of Clinical Cell Therapy (LTCC), Jules Bordet Institute , Université Libre de Bruxelles (ULB), Campus Erasme, Bâtiment de Transfusion (Level +1), Brussels, Belgium .

2 Department of Cell Biology (CYTO-VUB), Liver Cell Biology Laboratory, Vrije Universiteit Brussel , Brussels, Belgium .

出版信息

Tissue Eng Part C Methods. 2018 Feb;24(2):89-98. doi: 10.1089/ten.TEC.2017.0312. Epub 2018 Jan 16.

Abstract

Mesenchymal stromal cells (MSCs) have particular properties that allow their use as therapeutic strategies for several cell-based applications. Historically, bone marrow (BM)-MSCs are isolated by culture adherence since specific cell surface markers are yet to be developed. This original work aimed to identify and characterize isolating expanded BM-MSCs based on their aldehyde dehydrogenase (ALDH) activity known to be a hallmark of stem cells and relevant for their isolation. We thus isolated by fluorescence-activated cell sorting technology two functionally different populations of BM-MSCs depending on their ALDH activity (ALDH and ALDH). Transcriptome analysis and profiling clearly demonstrated that both populations of BM-MSCs present distinct pattern of genes related to the main properties of MSCs (proliferation, response to hypoxia, angiogenesis, phenotype, stemness, multilineage, hematopoiesis, immunomodulation) in an ALDH activity dependent manner. Both BM-MSC populations look to significantly differ in terms of biological responses and functionalities. More functional analyses are needed to understand and characterize the properties of these ALDH populations. Collectively, our results highlight ALDH activity as a potential feature for isolating and segregating functional and/or competent subset of BM-MSC populations, which may account for better and more efficient therapeutic issue.

摘要

间充质基质细胞 (MSCs) 具有特殊的性质,使其可用于几种基于细胞的应用的治疗策略。从历史上看,骨髓 (BM)-MSCs 通过培养粘附进行分离,因为尚未开发出特定的细胞表面标志物。这项原始工作旨在根据其醛脱氢酶 (ALDH) 活性鉴定和表征分离的扩增 BM-MSCs,已知 ALDH 活性是干细胞的标志,与它们的分离有关。因此,我们通过荧光激活细胞分选技术根据其 ALDH 活性(ALDH+和 ALDH-)分离了两种功能不同的 BM-MSC 群体。转录组分析和分析清楚地表明,两种 BM-MSC 群体均表现出与 MSC 的主要特性(增殖、对缺氧的反应、血管生成、表型、干性、多谱系、造血、免疫调节)相关的基因的独特模式,这与 ALDH 活性有关。这两种 BM-MSC 群体在生物学反应和功能方面似乎存在显著差异。需要进行更多的功能分析来理解和表征这些 ALDH 群体的特性。总之,我们的结果强调了 ALDH 活性作为分离和分离功能和/或有能力的 BM-MSC 群体的潜在特征,这可能有助于更好和更有效的治疗问题。

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