Beyond scoring: a modern interpretation of disease progression in chronic liver disease

Gut ◽  
2013 ◽  
Vol 62 (9) ◽  
pp. 1234-1241 ◽  
Author(s):  
Matteo Rosselli ◽  
Jane MacNaughtan ◽  
Rajiv Jalan ◽  
Massimo Pinzani
2017 ◽  
Author(s):  
Yi Xiong ◽  
Adriana Souza Torsoni ◽  
Feihua Wu ◽  
Hong Shen ◽  
Yan Liu ◽  
...  

SummaryHepatocyte replication maintains liver homeostasis and integrity. It is impaired in chronic liver disease, promoting disease progression. Herein, we have identified NF-kB-inducing kinase (NIK) as an unrecognized suppressor of hepatocyte replication. Hepatic NIK was aberrantly activated in chronic liver disease. Hepatocyte-specific deletion of NIK or its downstream mediator IKKα substantially accelerated hepatocyte proliferation and liver regeneration following partial hepatectomy. Mechanistically, NIK and IKKα suppressed the mitogenic JAK2/STAT3 pathway, thereby inhibiting hepatocyte cell cycle progression. Remarkably, inactivation of hepatic NIK largely reversed suppression of the hepatic JAK2/STAT3 pathway, hepatocyte replication, and liver regeneration induced by either chronic liver injury or metabolic stress. Our data suggest that hepatic NIK acts as a rheostat for liver regeneration to restrain liver overgrowth. Pathologic activation of hepatic NIK blocks hepatocyte replication, likely contributing to liver disease progression.


eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Yi Xiong ◽  
Adriana Souza Torsoni ◽  
Feihua Wu ◽  
Hong Shen ◽  
Yan Liu ◽  
...  

Reparative hepatocyte replication is impaired in chronic liver disease, contributing to disease progression; however, the underlying mechanism remains elusive. Here, we identify Map3k14 (also known as NIK) and its substrate Chuk (also called IKKα) as unrecognized suppressors of hepatocyte replication. Chronic liver disease is associated with aberrant activation of hepatic NIK pathways. We found that hepatocyte-specific deletion of Map3k14 or Chuk substantially accelerated mouse hepatocyte proliferation and liver regeneration following partial-hepatectomy. Hepatotoxin treatment or high fat diet feeding inhibited the ability of partial-hepatectomy to stimulate hepatocyte replication; remarkably, inactivation of hepatic NIK markedly increased reparative hepatocyte proliferation under these liver disease conditions. Mechanistically, NIK and IKKα suppressed the mitogenic JAK2/STAT3 pathway, thereby inhibiting cell cycle progression. Our data suggest that hepatic NIK and IKKα act as rheostats for liver regeneration by restraining overgrowth. Pathological activation of hepatic NIK or IKKα likely blocks hepatocyte replication, contributing to liver disease progression.


2013 ◽  
Vol 58 ◽  
pp. S460
Author(s):  
C. Paternostro ◽  
C. Busletta ◽  
C. Turato ◽  
S. Cannito ◽  
G. Villano ◽  
...  

2013 ◽  
Vol 45 ◽  
pp. S2
Author(s):  
C. Paternostro ◽  
C. Busletta ◽  
C. Turato ◽  
S. Cannito ◽  
A. Biasiolo ◽  
...  

2016 ◽  
Vol 48 (10) ◽  
pp. 1214-1219 ◽  
Author(s):  
Mònica Pons ◽  
Macarena Simón-Talero ◽  
Laura Millán ◽  
Meritxell Ventura-Cots ◽  
Begoña Santos ◽  
...  

2015 ◽  
Vol 36 (3) ◽  
pp. 370-377 ◽  
Author(s):  
Katharine M. Irvine ◽  
Leesa F. Wockner ◽  
Mihir Shanker ◽  
Kevin J. Fagan ◽  
Leigh U. Horsfall ◽  
...  

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