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支持miR-92a通过下调肝细胞生长因子来抑制脂肪来源间充质基质细胞血管生成活性的数据。

Data supporting that miR-92a suppresses angiogenic activity of adipose-derived mesenchymal stromal cells by down-regulating hepatocyte growth factor.

作者信息

Efimenko Anastassia, Sagaradze Georgiy, Akopyan Zhanna, Lopatina Tatiana, Kalinina Natalia

机构信息

Faculty of Medicine, Lomonosov Moscow State University, 31-5, Lomonosovsky av, Moscow 119191 Russia.

出版信息

Data Brief. 2015 Dec 17;6:295-310. doi: 10.1016/j.dib.2015.12.021. eCollection 2016 Mar.

DOI:10.1016/j.dib.2015.12.021
PMID:26862575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4706626/
Abstract

This article contains the full list of miRNAs expressed in cultured mesenchymal stromal cells, which were isolated from human adipose tissue. We provide here data regarding the effect of miR-92a overexpression on MSCs viability and cellular content of HGF and angiopoietin-1. These are followed by the data regarding the effect of conditioned medium of MSC transfected with pre-miR-92a, anti-miR-92a or scramble oligos on HUVEC viability as well as their tube formation efficiency. We also demonstrate here data regarding the effect of extracellular vesicle depletion from MSCs conditioned medium on its ability to stimulate the tube formation by HUVEC. Data interpretation and discussion can be found in Kalinina et al. (2015) [1].

摘要

本文包含了从人脂肪组织分离培养的间充质基质细胞中表达的miRNA完整列表。我们在此提供了关于miR-92a过表达对间充质干细胞活力以及肝细胞生长因子(HGF)和血管生成素-1细胞含量影响的数据。随后是关于用pre-miR-92a、抗miR-92a或乱序寡核苷酸转染的间充质干细胞条件培养基对人脐静脉内皮细胞(HUVEC)活力及其管形成效率影响的数据。我们还在此展示了关于从间充质干细胞条件培养基中去除细胞外囊泡对其刺激人脐静脉内皮细胞管形成能力影响的数据。数据解读和讨论可在Kalinina等人(2015年)[1]中找到。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/7f6315ff7e68/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/cb85e122de94/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/8cbe4d3b20e2/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/d39a2349ec74/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/55b67549288d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/7f6315ff7e68/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/cb85e122de94/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/8cbe4d3b20e2/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/d39a2349ec74/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/55b67549288d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8565/4706626/7f6315ff7e68/gr5.jpg

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本文引用的文献

1
miR-92a regulates angiogenic activity of adipose-derived mesenchymal stromal cells.微小RNA-92a调控脂肪来源间充质基质细胞的血管生成活性。
Exp Cell Res. 2015 Nov 15;339(1):61-6. doi: 10.1016/j.yexcr.2015.10.007. Epub 2015 Oct 20.
2
Multilineage cells from human adipose tissue: implications for cell-based therapies.来自人类脂肪组织的多谱系细胞:对基于细胞的疗法的意义。
Tissue Eng. 2001 Apr;7(2):211-28. doi: 10.1089/107632701300062859.
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Culture of human endothelial cells derived from umbilical veins. Identification by morphologic and immunologic criteria.
从间充质干细胞分化出内皮样细胞和平滑肌细胞用于阴道重建血管化的方法和机制
Mol Biotechnol. 2018 Jun;60(6):396-411. doi: 10.1007/s12033-018-0079-2.
4
Activation of β-adrenergic receptors is required for elevated α1A-adrenoreceptors expression and signaling in mesenchymal stromal cells.β-肾上腺素受体的激活是间质基质细胞中α1A-肾上腺素能受体表达和信号转导上调所必需的。
Sci Rep. 2016 Sep 6;6:32835. doi: 10.1038/srep32835.
源自脐静脉的人内皮细胞培养。通过形态学和免疫学标准进行鉴定。
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