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曲美他嗪和二氮嗪对人胚胎干细胞来源的间充质干细胞分泌组免疫调节活性的影响。

The effect of Trimetazidine and Diazoxide on immunomodulatory activity of human embryonic stem cell-derived mesenchymal stem cell secretome.

作者信息

Jahandideh Saeed, Maghsood Faezeh, Ghahhari Nastaran Mohammadi, Lotfinia Majid, Mohammadi Mohammad, Johari Behrooz, Kadivar Mehdi

机构信息

Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran.

Department of Biology, Basic Science Faculty, Shahid Chamran University, Ahvaz, Iran.

出版信息

Tissue Cell. 2017 Oct;49(5):597-602. doi: 10.1016/j.tice.2017.08.003. Epub 2017 Aug 16.

Abstract

Comprehensive proteome profiling of the factors secreted by mesenchymal stem cells (MSCs), referred to as secretome, revealed that it consists of cytokines, chemokines, growth factors, extracellular matrix proteins, and components of regeneration, vascularization, and hematopoiesis pathways. Harnessing this MSC secretome for therapeutic applications requires the optimization of production of secretary molecules. A variety of preconditioning methods have been introduced, which subject cells to stimulatory molecules to create the preferred response and stimulate persistent effects. Pharmacological preconditioning uses small molecules and drugs to increase survival of MSCs after transplantation or prolong release of effective secretary factors such as cytokines that improve immune system responses. In this study, we investigated the effect of secretome of human embryonic-derived mesenchymal stem cells (hESC-MSCs) preconditioned with Trimetazidine (TMZ) and Diazoxide (DZ) on immunomodulatory efficiency of these cells in LPS-induced peripheral blood mononuclear cells (PBMCs). PBMCs were isolated from human peripheral blood and treated with concentrated hESC-MSC-derived conditioned medium and then, the secreted levels of IL-10, TNFα and IL-1β were assessed by ELISA after induction with LPS. The results showed that TMZ and DZ-conditioned medium significantly enhanced immunomodulatory potential of hESC-MSCs by increasing the secretion of IL-10, TNFα and IL-1β from LPS- induced PBMCs. We also found that hESC-MSCs did not secrete mentioned cytokines prior to or after the preconditioning with TMZ and DZ. In conclusion, our results implied that TMZ and DZ can be used to promote the immunomodulatory effects of hESC-MSC secretome. It is obvious that for applying of these findings in clinical demands, the potency of different pre-conditioned MSCs secretome on immune response needs to be more clarified.

摘要

对间充质干细胞(MSC)分泌的因子进行全面的蛋白质组分析,即所谓的分泌组,结果显示其由细胞因子、趋化因子、生长因子、细胞外基质蛋白以及再生、血管生成和造血途径的成分组成。将这种MSC分泌组用于治疗应用需要优化分泌分子的产生。已经引入了多种预处理方法,这些方法使细胞接触刺激分子以产生优选的反应并刺激持续效应。药理学预处理使用小分子和药物来提高MSC移植后的存活率或延长有效分泌因子(如改善免疫系统反应的细胞因子)的释放。在本研究中,我们研究了用曲美他嗪(TMZ)和二氮嗪(DZ)预处理的人胚胎来源间充质干细胞(hESC-MSC)的分泌组对这些细胞在脂多糖(LPS)诱导的外周血单个核细胞(PBMC)中的免疫调节效率的影响。从人外周血中分离PBMC,并用浓缩的hESC-MSC来源的条件培养基处理,然后在用LPS诱导后通过酶联免疫吸附测定(ELISA)评估IL-10、TNFα和IL-1β的分泌水平。结果表明,TMZ和DZ预处理的培养基通过增加LPS诱导的PBMC中IL-10、TNFα和IL-1β的分泌,显著增强了hESC-MSC的免疫调节潜力。我们还发现,hESC-MSC在TMZ和DZ预处理之前或之后均不分泌上述细胞因子。总之,我们的结果表明TMZ和DZ可用于促进hESC-MSC分泌组的免疫调节作用。显然,为了将这些发现应用于临床需求,需要更明确不同预处理的MSC分泌组对免疫反应的效力。

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