Dietary therapy of murine primary biliary cholangitis induces hepatocellular steatosis: A cautionary tale

IF 6 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Weici Zhang, Taha Al Tekreeti, Patrick S. C. Leung, Koichi Tsuneyama, Harleen Dhillon, Manuel Rojas, Luke S. Heuer, William M. Ridgway, Aftab A. Ansari, Howard A. Young, Charles R. Mackay, M. Eric Gershwin
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引用次数: 0

Abstract

Background and Aims

There is increased interest in utilizing dietary interventions to alter the progression of autoimmune diseases. These efforts are driven by associations of gut microbiota/metabolites with levels of short-chain fatty acids (SCFAs). Propionate is a key SCFA that is commonly used as a food preservative and is endogenously generated by bacterial fermentation of non-digestible carbohydrates in the gut. A thesis has suggested that a diet rich in propionate and other SCFAs can successfully modulate autoimmunity. Herein, we investigated the effect of long-term administration of propionylated high-amylose resistant starches (HAMSP) on the course of murine primary biliary cholangitis.

Materials and Methods

Groups of female ARE-Del mice were fed an HAMSP diet either before or after disease onset. A detailed immunobiological analysis was performed involving autoantibodies and rigorous T-cell phenotyping, including enumeration of T-cell subsets in the spleen, liver, intestinal intraepithelial lymphocytes and lamina propria by flow cytometry. Histopathological scores were used to assess the frequency and severity of liver inflammation and damage to hepatocytes and bile ducts.

Results

Our results demonstrate that a long-term propionate-yielding diet re-populated the T-cell pool with decreased naïve and central memory T-cell subsets and an increase in the effector memory T cells in mice. Similarly, long-term HAMSP intake reduced CD4+CD8+ double-positive T cells in intraepithelial lymphocytes and the intestinal lamina propria. Critically, HAMSP consumption led to moderate-to-severe hepatocellular steatosis in ARE-Del mice, independent of the stage of autoimmune cholangitis.

Conclusions

Our data suggest that administration of HAMSP induces both regulatory and effector T cells. Furthermore, HAMSP administration resulted in hepatocellular steatosis. Given the interest in dietary modulation of autoimmunity and because propionate is widely used as a food preservative, these data have significant implications. This study also provides new insights into the immunological and pathological effects of chronic propionate exposure.

小鼠原发性胆汁性胆管炎的饮食疗法会诱发肝细胞脂肪变性:一个值得警惕的故事
背景和目的:人们越来越关注利用饮食干预来改变自身免疫性疾病的进展。肠道微生物群/代谢物与短链脂肪酸(SCFAs)水平的关联推动了这些研究工作。丙酸盐是一种关键的 SCFA,通常用作食品防腐剂,由肠道内非消化性碳水化合物的细菌发酵产生。有论文指出,富含丙酸盐和其他 SCFAs 的饮食可成功调节自身免疫。在此,我们研究了长期服用丙酸化高淀粉抗性淀粉(HAMSP)对小鼠原发性胆汁性胆管炎病程的影响:在发病前或发病后给雌性 ARE-Del 小鼠组喂食 HAMSP 食物。进行了详细的免疫生物学分析,包括自身抗体和严格的 T 细胞表型分析,包括通过流式细胞术枚举脾脏、肝脏、肠上皮内淋巴细胞和固有膜中的 T 细胞亚群。组织病理学评分用于评估肝脏炎症以及肝细胞和胆管损伤的频率和严重程度:我们的研究结果表明,长期摄入丙酸盐饮食会重新填充小鼠的 T 细胞池,减少幼稚和中心记忆 T 细胞亚群,增加效应记忆 T 细胞。同样,长期摄入 HAMSP 会减少上皮内淋巴细胞和肠道固有层中的 CD4+CD8+ 双阳性 T 细胞。重要的是,摄入 HAMSP 会导致 ARE-Del 小鼠出现中度至重度肝细胞脂肪变性,与自身免疫性胆管炎的阶段无关:我们的数据表明,服用 HAMSP 可诱导调节性和效应 T 细胞。此外,服用 HAMSP 会导致肝细胞脂肪变性。鉴于人们对饮食调节自身免疫的关注,以及丙酸盐被广泛用作食品防腐剂,这些数据具有重要意义。这项研究还为慢性丙酸盐暴露的免疫学和病理学影响提供了新的见解。
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来源期刊
Liver International
Liver International 医学-胃肠肝病学
CiteScore
13.90
自引率
4.50%
发文量
348
审稿时长
2 months
期刊介绍: Liver International promotes all aspects of the science of hepatology from basic research to applied clinical studies. Providing an international forum for the publication of high-quality original research in hepatology, it is an essential resource for everyone working on normal and abnormal structure and function in the liver and its constituent cells, including clinicians and basic scientists involved in the multi-disciplinary field of hepatology. The journal welcomes articles from all fields of hepatology, which may be published as original articles, brief definitive reports, reviews, mini-reviews, images in hepatology and letters to the Editor.
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