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High Concentrations of TNF-α Induce Cell Death during Interactions between Human Umbilical Cord Mesenchymal Stem Cells and Peripheral Blood Mononuclear Cells

机译:高浓度的TNF-α诱导人脐带间充质干细胞与外周血单个核细胞相互作用时细胞死亡

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摘要

Human umbilical cord mesenchymal stromal cells (hUC-MSCs) are currently being used as novel therapeutic agents in numerous clinical trials. Previous works have shown that hUC-MSCs possess profound immunomodulatory capacities through IL-1 stimulation produced by peripheral blood mononuclear cells (PBMCs), their main cellular partner in most pathophysiological and therapeutic situations. The present study was designed to explore the role of TNF-α in these interactions. In these experiments, we demonstrated that TNF-α originated from PBMCs under the influence of IL-1. We also showed that TNF-α acted differently depending upon the concentrations reached. At low concentrations it clearly contributed to IL-6 and monocyte chemotactic protein 1 (MCP-1) production. At high concentrations, used alone or in association with the TNF-related apoptosis-inducing ligand, TNF-α also stimulated hUC-MSC IL-6 but, more intensely, MCP-1 production. This stimulation was associated but independent of apoptosis induction in a process involving Inhibitor of Apoptosis Proteins. Interferon gamma (IFN-γ), tested to stimulate PBMC and tissue activation, amplified IL-6 and MCP-1 production and cell death by, apparently, a different process involving necrosis. Our findings bring new insights into the complex interactions between hUC-MSCs and PBMCs, involving cytokines, chemokines and cell death, and are of fundamental importance for tissue homeostasis.
机译:人脐带间充质基质细胞(hUC-MSC)目前在许多临床试验中被用作新型治疗剂。先前的研究表明,hUC-MSC通过外周血单核细胞(PBMC)产生的IL-1刺激具有强大的免疫调节能力,PBMC是大多数病理生理和治疗情况下的主要细胞伴侣。本研究旨在探讨TNF-α在这些相互作用中的作用。在这些实验中,我们证明了TNF-α在IL-1的影响下起源于PBMC。我们还表明,TNF-α的作用取决于达到的浓度。在低浓度下,它明显促进了IL-6和单核细胞趋化蛋白1(MCP-1)的产生。高浓度单独使用或与TNF相关的凋亡诱导配体结合使用时,TNF-α还能刺激hUC-MSC IL-6,但更能刺激MCP-1的产生。在涉及凋亡蛋白抑制剂的过程中,这种刺激是相关的,但与凋亡诱导无关。干扰素γ(IFN-γ)经过测试可刺激PBMC和组织激活,显然通过涉及坏死的不同过程放大了IL-6和MCP-1的产生以及细胞死亡。我们的发现为hUC-MSC与PBMC之间的复杂相互作用带来了新的见解,涉及细胞因子,趋化因子和细胞死亡,这对于组织动态平衡至关重要。

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