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Updated: Apr 30, 2026

Suppression of Pro-fibrotic Signaling Potentiates Factor-mediated Reprogramming of Mouse Embryonic Fibroblasts into Induced Cardiomyocytes
Published on: June 3, 2018
CBRH-7919 cell supernate promotes fibroblasts to express cyclooxygenase-2 and hepatocyte growth factor
1Department of Hepatobiliary Surgery, First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, People's Republic of China.
Background:
Transplanted cells need a microenvironment for proliferation and neovascularization. As an important component of the microenvironment, fibroblasts play a role in the process of tumor growth. With that in mind, we planned to activate fibroblasts in vitro and investigate the expression of cyclooxygenase-2 (COX-2) and hepatocyte growth factor (HGF) which can promote the proliferation and neovascularization of the transplanted liver cells.
Methods:
Fibroblasts were isolated from 20-day-old fetal Sprague-Dawley rats and incubated in the absence or presence of rat hepatoma CBRH-7919 cell supernate. On days 1, 2, 3, 5, and 7 the incubated fibroblasts were taken for detection of the levels of HGF and COX-2 by immunocytochemistry and the levels of HGF mRNA and COX-2 mRNA by reverse-transcription polymerase chain reaction.
Results:
When incubated in the presence of CBRH-7919 cell supernate, the fibroblasts could be activated to myofibroblasts that expressed alpha-smooth muscle actin at a high level, and the fibroblasts expressed COX-2, COX-2 mRNA, HGF, and HGF mRNA at higher levels, reaching a peak on day 3 and maintained at high levels until on day 7.
Conclusions:
Fibroblasts can be activated by CBRH-7919 cell supernate. Activated fibroblasts can express COX-2 and HGF at higher levels. Maybe we can take advantage of the activated fibroblasts to promote the neovascularization and proliferation of transplanted liver cells.
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