Journal
CELLS
Volume 9, Issue 3, Pages -Publisher
MDPI
DOI: 10.3390/cells9030558
Keywords
Src; saracatinib; PP2; liver fibrosis; HSC; TGF-beta; hepatocyte; CTGF; Smad3; autophagy
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Funding
- Korea Health technology R&D Project through the Korea Health Industry Development Institute (KHIDI) - Ministry of Health & Welfare, Republic of Korea [HI16C1501]
- National Research Foundation of Korea (NRF) - Korea Government (MSIP) [NRF-2018R1D1A1B07040372, NRF-2018R1A1A3A04078527]
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The SRC kinase family comprises non-receptor tyrosine kinases that are ubiquitously expressed in all cell types. Although Src is reportedly activated in pulmonary and renal fibrosis, little is known regarding its role in liver fibrosis. This study investigated whether the inhibition of Src protects against liver fibrosis. The expression of Src was upregulated in thioacetamide (TAA)-induced fibrotic mouse liver and cirrhosis of patients, and phospho-Src was upregulated during activation of hepatic stellate cells (HSC). In addition, Src inhibition reduced the expression of alpha-smooth muscle actin (alpha SMA) in primary HSCs and suppressed transforming growth factor beta (TGF-beta)-induced expression of connective tissue growth factor (CTGF) in hepatocytes. Src inhibitor Saracatinib also attenuated TAA-induced expression of type I collagen, alpha SMA, and CTGF in mouse liver tissues. The antifibrotic effect of Src inhibitors was associated with the downregulation of Smad3, but not of signal transducer and activator of transcription 3 (STAT3). In addition, Src inhibition increased autophagy flux and protected against liver fibrosis. These results suggest that Src plays an important role in liver fibrosis and that Src inhibitors could be treat liver fibrosis.
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