首页> 外文期刊>Frontiers in Immunology >d(?) Lactic Acid-Induced Adhesion of Bovine Neutrophils onto Endothelial Cells Is Dependent on Neutrophils Extracellular Traps Formation and CD11b Expression
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d(?) Lactic Acid-Induced Adhesion of Bovine Neutrophils onto Endothelial Cells Is Dependent on Neutrophils Extracellular Traps Formation and CD11b Expression

机译:d(?)牛中性粒细胞乳酸诱导的内皮细胞黏附取决于中性粒细胞胞外陷阱的形成和CD11b的表达

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Bovine ruminal acidosis is of economic importance as it contributes to reduced milk and meat production. This phenomenon is mainly attributed to an overload of highly fermentable carbohydrate, resulting in increased d(?) lactic acid levels in serum and plasma. Ruminal acidosis correlates with elevated acute phase proteins in blood, along with neutrophil activation and infiltration into various tissues leading to laminitis and aseptic polysynovitis. Previous studies in bovine neutrophils indicated that d(?) lactic acid decreased expression of L-selectin and increased expression of CD11b to concentrations higher than 6 mM, suggesting a potential role in neutrophil adhesion onto endothelia. The two aims of this study were to evaluate whether d(?) lactic acid influenced neutrophil and endothelial adhesion and to trigger neutrophil extracellular trap (NET) production (NETosis) in exposed neutrophils. Exposure of bovine neutrophils to 5 mM d(?) lactic acid elevated NET release compared to unstimulated neutrophil negative controls. Moreover, this NET contains CD11b and histone H4 citrullinated, the latter was dependent on PAD4 activation, a critical enzyme in DNA decondensation and NETosis. Furthermore, NET formation was dependent on d(?) lactic acid plasma membrane transport through monocarboxylate transporter 1 (MCT1). d(?) lactic acid enhanced neutrophil adhesion onto endothelial sheets as demonstrated by in vitro neutrophil adhesion assays under continuous physiological flow conditions, indicating that cell adhesion was a NET- and a CD11b/ICAM-1-dependent process. Finally, d(?) lactic acid was demonstrated for the first time to trigger NETosis in a PAD4- and MCT1-dependent manner. Thus, d(?) lactic acid-mediated neutrophil activation may contribute to neutrophil-derived pro-inflammatory processes, such as aseptic laminitis and/or polysynovitis in animals suffering acute ruminal acidosis.
机译:牛瘤胃酸中毒具有经济重要性,因为它有助于减少牛奶和肉类的产量。这种现象主要归因于高度可发酵的碳水化合物的超负荷,导致血清和血浆中乳酸(d)含量增加。瘤胃酸中毒与血液中急性期蛋白的升高,嗜中性粒细胞的活化和浸润进入各种组织相关,从而导致椎板炎和无菌性多囊炎。以前在牛嗜中性粒细胞中的研究表明,d(β)乳酸可降低L-选择素的表达,并增加CD11b的表达,使其浓度高于6 mM,表明在嗜中性粒细胞粘附到内皮上具有潜在作用。这项研究的两个目的是评估d(?)乳酸是否影响嗜中性粒细胞和内皮细胞的粘附,以及在暴露的嗜中性粒细胞中引发嗜中性粒细胞胞外捕集(NET)产生(NETosis)。与未刺激的嗜中性粒细胞阴性对照相比,牛嗜中性粒细胞暴露于5 mM d(α)乳酸可提高NET释放。此外,该NET包含CD11b和瓜氨酸化的组蛋白H4,后者依赖于PAD4活化,PAD4活化是DNA解聚和NETosis的关键酶。此外,NET的形成取决于通过单羧酸盐转运蛋白1(MCT1)的d(α)乳酸质膜的转运。 d(α)乳酸增强了嗜中性粒细胞在内皮层上的粘附,如在连续生理流动条件下进行的体外嗜中性粒细胞粘附测定所表明的那样,表明细胞粘附是依赖NET和CD11b / ICAM-1的过程。最后,首次证明了d(α)乳酸以PAD4和MCT1依赖性方式触发NETosis。因此,d(α)乳酸介导的嗜中性粒细胞活化可能导致中性粒细胞衍生的促炎过程,例如患有急性瘤胃酸中毒的动物中的无菌性层板炎和/或多发性滑膜炎。

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