Hepatocellular organellar abnormalities following elimination of hepatitis C virus

Author:

Aoyagi Haruyo1,Iijima Hiroko2,Gaber Eman S.1,Zaitsu Takuma1,Matsuda Mami1,Wakae Kosho1,Watashi Koichi1,Suzuki Ryosuke1,Masaki Takahiro13ORCID,Kahn Jeffrey4,Saito Takeshi4,El‐Kassas Mohamed5,Shimada Noritomo6,Kato Keizo7,Enomoto Masaru8,Hayashi Kazuhiko9ORCID,Tsubota Akihito10,Mimata Ayako11,Sakamaki Yuriko11,Ichinose Shizuko12,Muramatsu Masamichi1,Wake Kenjiro13,Wakita Takaji1,Aizaki Hideki1ORCID

Affiliation:

1. Department of Virology II National Institute of Infectious Diseases Tokyo Japan

2. Department of Internal Medicine, Division of Hepatobiliary and Pancreatic Disease Hyogo College of Medicine Hyogo Japan

3. Department of Laboratory Medicine The Jikei University School of Medicine Tokyo Japan

4. Department of Medicine, Division of Gastrointestinal and Liver Diseases, Keck School of Medicine University of Southern California Los Angeles California USA

5. Endemic Medicine Department, Faculty of Medicine Helwan University Cairo Egypt

6. Division of Gastroenterology and Hepatology Ootakanomori Hospital Chiba Japan

7. Division of Gastroenterology and Hepatology Shinmatsudo Central General Hospital Chiba Japan

8. Department of Hepatology Osaka Metropolitan University Osaka Japan

9. Division of Gastroenterology and Hepatology Meijo Hospital Nagoya Japan

10. Core Research Facilities, Research Center for Medical Science The Jikei University School of Medicine Tokyo Japan

11. Research Core Tokyo Medical and Dental University Tokyo Japan

12. Department of Plastic, Reconstructive and Aesthetic Surgery Nippon Medical School Tokyo Japan

13. Liver Research Unit Minophagen Pharmaceutical Co., Ltd. Tokyo Japan

Abstract

AbstractBackground and aimsThe future development of hepatocellular carcinoma (HCC) in patients after sustained virologic response (SVR) is an important issue. The purposes of this study were to investigate pathological alterations in organelle of the liver of SVR patients and to characterize organelle abnormalities that may be related to carcinogenesis after SVR.MethodsThe ultrastructure of liver biopsy specimens from patients with chronic hepatitis C (CHC) and SVR were compared to cell and mouse models and assessed semi‐quantitatively using transmission electron microscopy.ResultsHepatocytes in patients with CHC showed abnormalities in the nucleus, mitochondria, endoplasmic reticulum, lipid droplet, and pericellular fibrosis, comparable to those seen in hepatitis C virus (HCV)‐infected mice and cells. DAA treatment significantly reduced organelle abnormalities such as the nucleus, mitochondria, and lipid droplet in the hepatocytes of patients and mice after SVR, and cured cells, but it did not change dilated/degranulated endoplasmic reticulum and pericellular fibrosis in patients and mice after SVR. Further, samples from patients with a post‐SVR period of >1 year had significantly larger numbers of abnormalities in the mitochondria and endoplasmic reticulum than those of <1 year. A possible cause of organelle abnormalities in patients after SVR could be oxidative stress of the endoplasmic reticulum and mitochondria associated with abnormalities of the vascular system due to fibrosis. Interestingly, abnormal endoplasmic reticulum was associated with patients with HCC for >1 year after SVR.ConclusionsThese results indicate that patients with SVR exhibit a persistent disease state and require long‐term follow‐up to detect early signs of carcinogenesis.

Publisher

Wiley

Subject

Hepatology

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