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在注射脐带血源性间充质干细胞后的野百合碱诱导的肺动脉高压大鼠中的基因芯片分析

Microarray analysis after umbilical cord blood derived mesenchymal stem cells injection in monocrotaline-induced pulmonary artery hypertension rats.

作者信息

Lee Jae Chul, Kim Kwan Chang, Yang Yoon Sun, Oh Wonil, Choi Soo Jin, Choe Soo Young, Hong Young Mi

机构信息

Department of Pediatrics, Ewha Womans University School of Medicine, Seoul, Korea. ; Department of Biology, School of Life Sciences, Chungbuk National University, Cheongju, Korea.

Department of Thoracic and Cardiovascular Surgery, Ewha Womans University School of Medicine, Seoul, Korea.

出版信息

Anat Cell Biol. 2014 Dec;47(4):217-26. doi: 10.5115/acb.2014.47.4.217. Epub 2014 Dec 23.

Abstract

Pulmonary arterial hypertension (PAH) is associated with structural alterations of lung vasculature. PAH is still a devastating disease needing an aggressive therapeutic approach. Despite the therapeutic potential of human umbilical cord mesenchymal stem cells (MSCs), the molecular parameters to define the stemness remain largely unknown. Using high-density oligonucleotide microarrays, the differential gene expression profiles between a fraction of mononuclear cells of human umbilical cord blood (UCB) and its MSC subpopulation were obtained. Of particular interest was a subset of 46 genes preferentially expressed at 7-fold or higher in the group treated with human UCB-MSCs. This subset contained numerous genes involved in the inflammatory response, immune response, lipid metabolism, cell adhesion, cell migration, cell differentiation, apoptosis, cell growth, transport, cell proliferation, transcription, and signal transduction. Our results provide a foundation for a more reproducible and reliable quality control using genotypic analysis for the definition of human UCB-MSCs. Therefore, our results will provide a basis for studies on molecular mechanisms controlling the core properties of human MSCs.

摘要

肺动脉高压(PAH)与肺血管结构改变相关。PAH仍然是一种需要积极治疗方法的毁灭性疾病。尽管人脐带间充质干细胞(MSCs)具有治疗潜力,但定义干性的分子参数在很大程度上仍然未知。利用高密度寡核苷酸微阵列,获得了人脐带血(UCB)单核细胞部分与其MSC亚群之间的差异基因表达谱。特别令人感兴趣的是一组46个基因的子集,这些基因在用人类UCB-MSCs处理的组中优先以7倍或更高的水平表达。该子集包含许多参与炎症反应、免疫反应、脂质代谢、细胞粘附、细胞迁移、细胞分化、凋亡、细胞生长、转运、细胞增殖、转录和信号转导的基因。我们的结果为使用基因分型分析来定义人UCB-MSCs提供了更可重复和可靠的质量控制基础。因此,我们的结果将为研究控制人MSCs核心特性的分子机制提供基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ecc/4276895/c46aead28d5e/acb-47-217-g001.jpg

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