COL6A3-derived endotrophin links reciprocal interactions among hepatic cells in the pathology of chronic liver disease
Autor: | Jang Hyun Choi, Sang Min Lee, Jun Ho Lee, Philipp E. Scherer, Min Kim, Hyun Hee Shin, Jiyoung Oh, Jiyoung Park, Changhu Lee, Hyug Moo Kwon |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
business.industry Inflammation Chronic liver disease medicine.disease Pathology and Forensic Medicine Pathogenesis 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Fibrosis 030220 oncology & carcinogenesis Hepatocellular carcinoma medicine Hepatic stellate cell Cancer research Biomarker (medicine) medicine.symptom Hepatic fibrosis business |
Zdroj: | The Journal of Pathology. 247:99-109 |
ISSN: | 0022-3417 |
Popis: | Extracellular matrix dysregulation is associated with chronic liver disease. CollagenVI-alpha3 chain (COL6A3) is a biomarker for hepatic fibrosis and poor prognosis of hepatocellular carcinoma (HCC), but its function in liver pathology remains unknown. High levels of COL6A3 and its cleaved product, endotrophin (ETP) in tumor-neighboring regions are strongly associated with poor prognosis in HCC patients. Here, we report that the high levels of ETP in injured hepatocytes induce JNK-dependent hepatocyte apoptosis and activate nonparenchymal cells to lead further activation of hepatic inflammation, fibrosis, and apoptosis. Nevertheless ETP per se showed limited phenotypic changes in normal liver tissues. Furthermore, inhibition of ETP activity by utilizing neutralizing antibodies efficiently suppressed the pathological consequences in chronic liver diseases. Our results implicate ETP mechanistically as a crucial mediator in reciprocal interactions among various hepatic cell populations in the pathogenesis of chronic liver disease, and it could be a promising therapeutic target particularly in individuals with high local levels of COL6A3. Copyright © 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. |
Databáze: | OpenAIRE |
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