scholarly journals Cluster of Differentiation 44 Promotes Liver Fibrosis and Serves as a Biomarker in Congestive Hepatopathy

2021 ◽  
Author(s):  
Yosuke Osawa ◽  
Hironari Kawai ◽  
Tomoyuki Tsunoda ◽  
Haruki Komatsu ◽  
Miku Okawara ◽  
...  
2020 ◽  
Vol 21 (24) ◽  
pp. 9420
Author(s):  
José Ignacio Fortea ◽  
Ángela Puente ◽  
Antonio Cuadrado ◽  
Patricia Huelin ◽  
Raúl Pellón ◽  
...  

Liver disease resulting from heart failure (HF) has generally been referred as “cardiac hepatopathy”. One of its main forms is congestive hepatopathy (CH), which results from passive venous congestion in the setting of chronic right-sided HF. The current spectrum of CH differs from earlier reports with HF, due to ischemic cardiomyopathy and congenital heart disease having surpassed rheumatic valvular disease. The chronic passive congestion leads to sinusoidal hypertension, centrilobular fibrosis, and ultimately, cirrhosis (“cardiac cirrhosis”) and hepatocellular carcinoma after several decades of ongoing injury. Contrary to primary liver diseases, in CH, inflammation seems to play no role in the progression of liver fibrosis, bridging fibrosis occurs between central veins to produce a “reversed lobulation” pattern and the performance of non-invasive diagnostic tests of liver fibrosis is poor. Although the clinical picture and prognosis is usually dominated by the underlying heart condition, the improved long-term survival of cardiac patients due to advances in medical and surgical treatments are responsible for the increased number of liver complications in this setting. Eventually, liver disease could become as clinically relevant as cardiac disease and further complicate its management.


2020 ◽  
Vol 73 ◽  
pp. S518
Author(s):  
Hironari Kawai ◽  
Yosuke Osawa ◽  
Yuriko Tsutsui ◽  
Yuichi Yoshida ◽  
Taizo Mori ◽  
...  

Author(s):  
Joshua A. Rushakoff ◽  
Evan P. Kransdorf ◽  
Jignesh K. Patel ◽  
Jon A. Kobashigawa ◽  
Vinay Sundaram ◽  
...  

2021 ◽  
Vol 30 ◽  
pp. 096368972110040
Author(s):  
Weina Li ◽  
Fei He

Transfer of exogenous macrophages represents an alternative technique to treat liver fibrosis. At present, bone marrow-derived monocytes and stem cells are the main sources for exogenous macrophages. Kupffer cells (KCs) are the resident macrophages in the liver and play a critical role in the liver homeostasis and diseases. It is unclear whether infusion of KCs can treat liver fibrosis. In this study, we observed that granulocyte-macrophage colony stimulating factor (GM-CSF) could improve the purity of cultured KCs and significantly up-regulate the expression of Cluster of Differentiation 11b (CD11b). The most important point is that GM-CSF could significantly promote the proliferation of KCs in vitro. KCs expanded in vitro still had the potential of M1/M2 polarization and phagocytosis. Furthermore, infusion of these KCs could ameliorate liver fibrosis induced by carbon tetrachloride (CCl4) in mice. Together, our results suggest that KCs are likely to be another source for macrophage therapy.


Hepatology ◽  
2021 ◽  
Author(s):  
Hironari Kawai ◽  
Yosuke Osawa ◽  
Michitaka Matsuda ◽  
Tomoyuki Tsunoda ◽  
Keisuke Yanagida ◽  
...  

2005 ◽  
Vol 35 (6) ◽  
pp. 68-69
Author(s):  
JEFF EVANS
Keyword(s):  

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