An anti-eCIRP strategy for necrotizing enterocolitis.

IF 6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Colleen P Nofi, Jose M Prince, Mariana R Brewer, Monowar Aziz, Ping Wang
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引用次数: 0

Abstract

Background: Necrotizing enterocolitis (NEC) is a severe gastrointestinal disease characterized by intestinal inflammation and injury, with high mortality risk. Extracellular cold-inducible RNA-binding protein (eCIRP) is a recently discovered damage-associated molecular pattern that propagates inflammation and tissue injury; however, the role of eCIRP in NEC remains unknown. We hypothesize that eCIRP exacerbates NEC pathogenesis and the novel eCIRP-scavenging peptide, milk fat globule-epidermal growth factor-factor VIII (MFG-E8)-derived oligopeptide 3 (MOP3), attenuates NEC severity, serving as a new therapeutic strategy to treat NEC.

Methods: Stool samples from premature neonates were collected prospectively and eCIRP levels were measured. Wild-type (WT) and CIRP-/- mouse pups were subjected to NEC utilizing a combination of hypoxia and hypercaloric formula orogastric gavage with lipopolysaccharide supplementation. In parallel, WT pups were treated with MOP3 or vehicle. Endpoints including NEC severity, intestinal injury, barrier dysfunction, lung injury, and overall survival were determined.

Results: Stool samples from NEC neonates had elevated eCIRP levels compared to healthy age-matched controls (p < 0.05). CIRP-/- pups were significantly protected from NEC severity, intestinal injury, bowel inflammation, intestinal barrier dysfunction, lung injury, and systemic inflammation. NEC survival was 100% for CIRP-/- pups compared to 65% for WT (p < 0.05). MOP3 treatment recapitulated the benefits afforded by CIRP-knockdown, preventing NEC severity, improving inflammatory profiles, and attenuating organ injury. MOP3 treatment improved NEC survival to 80% compared to 50% for vehicle treatment (p < 0.05).

Conclusions: eCIRP exacerbates NEC evidenced by protection with CIRP-deficiency and administration of MOP3, a CIRP-directed therapeutic, in a murine model. Thus, eCIRP is a novel target with human relevance, and MOP3 is a promising treatment for lethal NEC.

针对坏死性小肠结肠炎的抗 eCIRP 策略。
背景:坏死性小肠结肠炎(NEC坏死性小肠结肠炎(NEC)是一种以肠道炎症和损伤为特征的严重胃肠道疾病,死亡率很高。细胞外冷诱导 RNA 结合蛋白(eCIRP)是最近发现的一种损伤相关分子模式,可传播炎症和组织损伤;然而,eCIRP 在坏死性小肠结肠炎中的作用仍然未知。我们假设 eCIRP 会加剧 NEC 的发病机制,而新型 eCIRP 清除肽--乳脂球-表皮生长因子-因子 VIII(MFG-E8)衍生的寡肽 3(MOP3)--会减轻 NEC 的严重程度,从而成为治疗 NEC 的新疗法:方法:对早产新生儿的粪便样本进行前瞻性采集,并测定 eCIRP 水平。对野生型(WT)和 CIRP-/- 小鼠幼崽进行 NEC 试验,采用缺氧和高热量配方口服结合补充脂多糖的方法。与此同时,WT幼鼠接受MOP3或药物治疗。终点包括NEC严重程度、肠道损伤、屏障功能障碍、肺损伤和总存活率:结果:与健康的年龄匹配对照组相比,NEC 新生儿粪便样本中的 eCIRP 水平升高(p -/-幼崽在 NEC 严重程度、肠道损伤、肠道炎症、肠道屏障功能障碍、肺损伤和全身炎症方面受到显著保护。CIRP-/- 幼崽的 NEC 存活率为 100%,而 WT 幼崽的存活率为 65%(p 结论:在小鼠模型中,CIRP 缺失和给予 MOP3(一种 CIRP 引导的疗法)的保护证明了 eCIRP 会加重 NEC。因此,eCIRP 是一个与人类相关的新靶点,而 MOP3 是一种治疗致命性 NEC 的有前途的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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