Pedrazza Leonardo, Cunha Aline Andrea, Luft Carolina, Nunes Nailê Karine, Schimitz Felipe, Gassen Rodrigo Benedetti, Breda Ricardo Vaz, Donadio Marcio Vinícius Fagundes, de Souza Wyse Angela Terezinha, Pitrez Paulo Marcio Condessa, Rosa Jose Luis, de Oliveira Jarbas Rodrigues
Laboratório de Pesquisa em Biofísica Celular e Inflamação, Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Rio Grande do Sul, Brazil.
Laboratório de Respirologia Pediátrica, Centro Infant, Instituto de Pesquisas Biomédicas (IPB), Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Rio Grande do Sul, Brazil.
J Cell Physiol. 2017 Dec;232(12):3552-3564. doi: 10.1002/jcp.25816. Epub 2017 Feb 9.
Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are syndromes of acute hypoxemic respiratory failure resulting from a variety of direct and indirect injuries to the gas exchange parenchyma of the lungs. During the ALI, we have an increase release of proinflammatory cytokines and high reactive oxygen species (ROS) formation. These factors are responsible for the release and activation of neutrophil-derived proteases and the formation of neutrophil extracellular traps (NETs). The excessive increase in the release of NETs cause damage to lung tissue. Recent studies have studies involving the administration of mesenchymal stem cells (MSCs) for the treatment of experimental ALI has shown promising results. In this way, the objective of our study is to evaluate the ability of MSCs, in a lipopolysaccharide (LPS)-induced ALI model, to reduce inflammation, oxidative damage, and consequently decrease the release of NETs. Mice were submitted lung injury induced by intratracheal instillation of LPS and subsequently treated or not with MSCs. Treatment with MSCs was able to modulate pulmonary inflammation, decrease oxidative damage, and reduce the release of NETs. These benefits from treatment are evident when we observe a significant increase in the survival curve in the treated animals. Our results demonstrate that MSCs treatment is effective for the treatment of ALI. For the first time, it is described that MSCs can reduce the formation of NETs and an experimental model of ALI. This finding is directly related to these cells modulate the inflammatory response and oxidative damage in the course of the pathology.
急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)是由肺部气体交换实质的各种直接和间接损伤导致的急性低氧性呼吸衰竭综合征。在ALI期间,促炎细胞因子的释放增加,活性氧(ROS)大量生成。这些因素导致中性粒细胞衍生蛋白酶的释放和激活以及中性粒细胞胞外陷阱(NETs)的形成。NETs释放的过度增加会对肺组织造成损害。最近涉及给予间充质干细胞(MSCs)治疗实验性ALI的研究显示出了有前景的结果。通过这种方式,我们研究的目的是评估在脂多糖(LPS)诱导的ALI模型中,MSCs减轻炎症、氧化损伤并进而减少NETs释放的能力。通过气管内滴注LPS诱导小鼠发生肺损伤,随后对其进行或不进行MSCs治疗。MSCs治疗能够调节肺部炎症,减少氧化损伤,并减少NETs的释放。当我们观察到治疗组动物的生存曲线显著上升时,治疗带来的这些益处就很明显了。我们的结果表明,MSCs治疗对ALI有效。首次描述了MSCs可以减少NETs的形成以及ALI的实验模型。这一发现与这些细胞在病理过程中调节炎症反应和氧化损伤直接相关。