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肠细胞中 IKKβ 的抑制会加剧脓毒症引起的肠道损伤,并使死亡率恶化。

Inhibition of IKKβ in enterocytes exacerbates sepsis-induced intestinal injury and worsens mortality.

机构信息

1Department of Anesthesiology, University of Colorado Anschutz Medical Campus, Aurora, CO. 2Department of Surgery, Washington University School of Medicine, St. Louis, MO. 3Emory Center for Critical Care and Department of Surgery, Emory Healthcare and Emory University School of Medicine, Atlanta, GA. 4Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA.

出版信息

Crit Care Med. 2013 Oct;41(10):e275-85. doi: 10.1097/CCM.0b013e31828a44ed.

Abstract

OBJECTIVES

Nuclear factor-κB is a critical regulator of cell-survival genes and the host inflammatory response. The purpose of this study was to investigate the role of enterocyte-specific NF-kB in sepsis through selective ablation of IkB kinase.

DESIGN

Prospective, randomized controlled study.

SETTING

Animal laboratories in university medical centers.

SUBJECTS AND INTERVENTIONS

Mice lacking functional NF-kB in their intestinal epithelium (Vil-Cre/Ikkβ) and wild-type mice were subjected to sham laparotomy or cecal ligation and puncture. Animals were killed at 24 hours or followed 7 days for survival.

MEASUREMENTS AND MAIN RESULTS

Septic wild-type mice had decreased villus length compared with sham mice, whereas villus atrophy was further exacerbated in septic Vil-Cre/Ikkβ mice. Sepsis induced an increase in intestinal epithelial apoptosis compared with sham mice, which was further exacerbated in Vil-Cre/Ikkβ mice. Sepsis induced intestinal hyperpermeability in wild-type mice compared with sham mice, which was further exacerbated in septic Vil-Cre/Ikkβ mice. This was associated with increased intestinal expression of claudin-2 in septic wild-type mice, which was further increased in septic Vil-Cre/Ikkβ mice. Both, pro-inflammatory and anti-inflammatory cytokines were increased in serum following cecal ligation and puncture, and interleukin 10 and monocyte chemoattractant protein-1 levels were higher in septic Vil-Cre/Ikkβ mice than in septic wild-type mice. All septic mice were bacteremic, but no differences in bacterial load were identified between wild-type and Vil-Cre/Ikkβ mice. To determine the functional significance of these results, animals were followed for survival. Septic wild-type mice had lower mortality than septic Vil-Cre/Ikkβ mice (47% vs 80%, p<0.05). Antitumor necrosis factor administration decreased intestinal apoptosis, permeability, and mortality in wild-type septic mice, and a similar improvement in intestinal integrity and survival were seen when antitumor necrosis factor was given to Vil-Cre/Ikkβ mice.

CONCLUSIONS

Enterocyte-specific NF-kB has a beneficial role in sepsis by partially preventing sepsis-induced increases in apoptosis and permeability, which are associated with worsening mortality.

摘要

目的

核因子-κB 是细胞存活基因和宿主炎症反应的关键调节因子。本研究旨在通过选择性消融 IkB 激酶来研究肠上皮细胞特异性 NF-κB 在脓毒症中的作用。

设计

前瞻性、随机对照研究。

地点

大学医学中心的动物实验室。

对象和干预措施

缺乏肠道上皮 NF-κB 功能的小鼠(Vil-Cre/Ikkβ)和野生型小鼠接受假手术或盲肠结扎和穿孔。动物在 24 小时或 7 天后死亡以进行存活观察。

测量和主要结果

与假手术组相比,脓毒症野生型小鼠的绒毛长度降低,而脓毒症 Vil-Cre/Ikkβ 小鼠的绒毛萎缩进一步加重。与假手术组相比,脓毒症诱导的肠上皮细胞凋亡增加,而 Vil-Cre/Ikkβ 小鼠的凋亡进一步加重。与假手术组相比,脓毒症诱导的野生型小鼠肠道通透性增加,而脓毒症 Vil-Cre/Ikkβ 小鼠的通透性进一步增加。这与脓毒症野生型小鼠肠道 Claudin-2 表达增加有关,而脓毒症 Vil-Cre/Ikkβ 小鼠的 Claudin-2 表达进一步增加。盲肠结扎和穿孔后血清中促炎和抗炎细胞因子均增加,脓毒症 Vil-Cre/Ikkβ 小鼠的白细胞介素 10 和单核细胞趋化蛋白-1 水平高于脓毒症野生型小鼠。所有脓毒症小鼠均发生菌血症,但野生型和 Vil-Cre/Ikkβ 小鼠之间的细菌负荷无差异。为了确定这些结果的功能意义,动物被观察存活。与脓毒症 Vil-Cre/Ikkβ 小鼠相比,脓毒症野生型小鼠的死亡率较低(47%比 80%,p<0.05)。抗肿瘤坏死因子治疗降低了野生型脓毒症小鼠的肠细胞凋亡、通透性和死亡率,当给予 Vil-Cre/Ikkβ 小鼠抗肿瘤坏死因子时,也观察到肠完整性和存活率的类似改善。

结论

肠上皮细胞特异性 NF-κB 在脓毒症中具有有益作用,可部分预防脓毒症引起的凋亡和通透性增加,从而降低死亡率。

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