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Wound trauma mediated inflammatory signaling attenuates a tissue regenerative response in MRL/MpJ mice

机译:伤口创伤介导的炎症信号减弱了MRL / MpJ小鼠的组织再生反应

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Background Severe trauma can induce pathophysiological responses that have marked inflammatory components. The development of systemic inflammation following severe thermal injury has been implicated in immune dysfunction, delayed wound healing, multi-system organ failure and increased mortality. Methods In this study, we examined the impact of thermal injury-induced systemic inflammation on the healing response of a secondary wound in the MRL/MpJ mouse model, which was anatomically remote from the primary site of trauma, a wound that typically undergoes scarless healing in this specific strain. Ear-hole wounds in MRL/MpJ mice have previously displayed accelerated healing and tissue regeneration in the absence of a secondary insult. Results Severe thermal injury in addition to distal ear-hole wounds induced marked local and systemic inflammatory responses in the lungs and significantly augmented the expression of inflammatory mediators in the ear tissue. By day 14, 61% of the ear-hole wounds from thermally injured mice demonstrated extensive inflammation with marked inflammatory cell infiltration, extensive ulceration, and various level of necrosis to the point where a large percentage (38%) had to be euthanized early during the study due to extensive necrosis, inflammation and ear deformation. By day 35, ear-hole wounds in mice not subjected to thermal injury were completely closed, while the ear-hole wounds in thermally injured mice exhibited less inflammation and necrosis and only closed partially (62%). Thermal injury resulted in marked increases in serum levels of IL-6, TNFα, KC (CXCL1), and MIP-2α (CXCL2). Interestingly, attenuated early ear wound healing in the thermally injured mouse resulted in incomplete tissue regeneration in addition to a marked inflammatory response, as evidenced by the histological appearance of the wound and increased transcription of potent inflammatory mediators. Conclusion These findings suggest that the observed systemic inflammatory response of a severe thermal injury undoubtedly has an adverse effect on wound healing and tissue regeneration.
机译:背景严重的外伤可引起具有明显炎症成分的病理生理反应。严重热损伤后全身炎症的发展与免疫功能障碍,伤口愈合延迟,多系统器官衰竭和死亡率增加有关。方法在本研究中,我们在MRL / MpJ小鼠模型中检查了热损伤引起的全身炎症对继发性伤口愈合反应的影响,该模型在解剖学上远离创伤的主要部位,该伤口通常经历无疤痕愈合在这个特定的应变。在没有第二次侮辱的情况下,MRL / MpJ小鼠的耳孔伤口先前已显示出加速的愈合和组织再生。结果除远端耳孔伤口外,严重的热损伤还引起肺部明显的局部和全身炎症反应,并显着增强了耳组织中炎症介质的表达。到第14天,来自热损伤小鼠的耳孔伤口中有61%表现出广泛的炎症反应,并伴有明显的炎症细胞浸润,广泛的溃疡形成和各种程度的坏死,以致在早期必须对大比例(38%)实施安乐死该研究由于广泛的坏死,炎症和耳朵变形。到第35天,未遭受热损伤的小鼠的耳孔伤口已完全闭合,而受到热损伤的小鼠的耳孔伤口表现出较少的炎症和坏死,仅部分闭合(62%)。热损伤导致血清IL-6,TNFα,KC(CXCL1)和MIP-2α(CXCL2)的水平明显升高。有趣的是,热损伤小鼠的早期耳朵伤口愈合减弱,除了明显的炎症反应外,还导致组织再生不完全,伤口的组织学表现和有效的炎症介质转录增加证明了这一点。结论这些发现表明,观察到的严重热损伤的全身炎症反应无疑对伤口愈合和组织再生有不利影响。

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