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人骨髓间充质干细胞/基质细胞暴露于炎症环境中会增加 ICAM-1 的表达并释放富含这种黏附分子的微囊泡:分析 TNF-α 和 IFN- 的参与。

Human Bone Marrow Mesenchymal Stem/Stromal Cells Exposed to an Inflammatory Environment Increase the Expression of ICAM-1 and Release Microvesicles Enriched in This Adhesive Molecule: Analysis of the Participation of TNF- and IFN-.

机构信息

Mesenchymal Stem Cells Laboratory, Oncology Research Unit, Oncology Hospital, National Medical Center (IMSS), Mexico City C.P. 06720, Mexico.

Immunology and Stem Cells Laboratory, FES Zaragoza, National Autonomous University of Mexico (UNAM), Mexico City C.P. 09230, Mexico.

出版信息

J Immunol Res. 2020 Nov 30;2020:8839625. doi: 10.1155/2020/8839625. eCollection 2020.

Abstract

Bone marrow mesenchymal stem/stromal cells (BM-MSCs) have immunoregulatory capacity; therefore, they have been used in different clinical protocols in which it is necessary to decrease the immune response. This capacity is mainly regulated by TNF- and IFN-, and it has been observed that cell-cell contact, mainly mediated by ICAM-1, is important for MSCs to carry out efficient immunoregulation. Therefore, in the present work, we analyzed the effect of TNF- alone or in combination with IFN- on the expression of ICAM-1. Besides, given the importance of cell contact in the immunoregulatory function of MSCs, we analyzed whether these cells release ICAM-1 microvesicles (MVs). Our results show for the first time that TNF- is capable of increasing the early expression of ICAM-1 in human BM-MSCs. Also, we observed that TNF- and IFN- have a synergistic effect on the increase in the expression of ICAM-1. Furthermore, we found that BM-MSCs exposed to an inflammatory environment release MVs enriched in ICAM-1 (MVs-ICAM-1). The knowledge generated in this study will contribute to the improvement of conditioning protocols that favor the therapeutic effect of these cells or their products.

摘要

骨髓间充质干细胞(BM-MSCs)具有免疫调节能力;因此,它们已被用于不同的临床方案中,这些方案需要降低免疫反应。这种能力主要受 TNF-α 和 IFN-调控,并且已经观察到细胞间接触,主要由 ICAM-1 介导,对于 MSCs 进行有效的免疫调节很重要。因此,在本工作中,我们分析了 TNF-α 单独或与 IFN-联合对 ICAM-1 表达的影响。此外,鉴于细胞接触在 MSCs 的免疫调节功能中的重要性,我们分析了这些细胞是否释放含有 ICAM-1 的微泡(MVs)。我们的结果首次表明,TNF-α 能够增加人 BM-MSCs 中 ICAM-1 的早期表达。此外,我们观察到 TNF-α 和 IFN-对 ICAM-1 表达的增加具有协同作用。此外,我们发现暴露于炎症环境中的 BM-MSCs 释放富含 ICAM-1 的微泡(MVs-ICAM-1)。本研究产生的知识将有助于改进有利于这些细胞或其产物治疗效果的调理方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/7723491/a5a9fa7e77d0/JIR2020-8839625.001.jpg

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