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代谢功能障碍相关脂肪性肝病中细胞内细胞器的异常

Abnormalities of intracellular organelles in metabolic dysfunction-associated steatotic disease.

作者信息

Kido Hidenori, Mizukoshi Eishiro, Yanagi Masahiro, Shihui Li, Seike Takuya, Nakagawa Hidetoshi, Yamashima Tetsumori, Shiraishi Yoshitake, Ozaki Noriyuki, Harada Kenichi, Okada Hikari, Goto Hisanori, Kimura Kumi, Yamamoto Yasuhiko, Yamashita Taro

机构信息

Department of Gastroenterology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Ishikawa, Japan.

Department of Psychiatry and Behavioral Science, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Ishikawa, Japan.

出版信息

J Gastroenterol. 2025 May 9. doi: 10.1007/s00535-025-02257-5.

Abstract

BACKGROUND

The concept of metabolic dysfunction-associated steatotic disease (MASLD) is increasingly being recognized. The mechanisms contributing to hepatocellular injury include oxidative stress owing to mitochondrial dysfunction, endoplasmic reticulum (ER) stress owing to abnormal protein accumulation in the rough ER, and disruption of cellular homeostasis and metabolic regulation to autophagic dysfunction. However, the morphological abnormalities of these intracellular organelles remain unclear.

METHODS

Liver tissues from model mice of MASLD, patients with MASLD, and respective controls were subjected to histopathological examination using light microscopy, and intracellular organelles were analyzed via transmission electron microscopy (TEM).

RESULTS

In model mice of MASLD, the progression of MASLD pathology was associated with abnormalities in mitochondria, glycogen granules, and rough ER. Based on these findings, the electron microscopic observations of these intracellular organelles were classified, weighted, and evaluated in liver tissues of patients with MASLD. The electron microscopic findings were significantly relatively frequent in patients with MASLD and correlated with existing histopathological scoring.

CONCLUSIONS

Using TEM, we identified characteristic abnormalities in intracellular organelles specific to MASLD. These findings contribute to the understanding of the mechanisms underlying hepatocellular injury in MASLD.

摘要

背景

代谢功能障碍相关脂肪性肝病(MASLD)的概念日益受到认可。导致肝细胞损伤的机制包括线粒体功能障碍引起的氧化应激、粗面内质网中蛋白质异常积累导致的内质网(ER)应激,以及细胞内稳态和代谢调节因自噬功能障碍而受到破坏。然而,这些细胞内细胞器的形态学异常仍不清楚。

方法

对MASLD模型小鼠、MASLD患者及各自的对照的肝组织进行光学显微镜组织病理学检查,并通过透射电子显微镜(TEM)分析细胞内细胞器。

结果

在MASLD模型小鼠中,MASLD病理进展与线粒体、糖原颗粒和粗面内质网异常有关。基于这些发现,对MASLD患者肝组织中这些细胞内细胞器的电子显微镜观察结果进行分类、加权和评估。电子显微镜检查结果在MASLD患者中显著相对常见,且与现有的组织病理学评分相关。

结论

通过透射电子显微镜,我们确定了MASLD特有的细胞内细胞器特征性异常。这些发现有助于理解MASLD中肝细胞损伤的潜在机制。

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