Apoptotic Body Engulfment by a Human Stellate Cell Line Is Profibrogenic

• DOI: 10.1097/01.lab.0000069036.63405.5c
• Publication Date: 2013-09-04T18:33:22Z
• Authors: Ali Canbay; Pavel Taimr; Natalie Torok; Hajime Higuchi; Scott Friedman; Gregory J Gores
• Keywords: Liver Cirrhosis; 0301 basic medicine; Nocodazole; Apoptosis; Microtubules; p38 Mitogen-Activated Protein Kinases; Collagen Type I; Cell Line; Transforming Growth Factor beta1; Phosphatidylinositol 3-Kinases; 03 medical and health sciences; Transforming Growth Factor beta; Hepatocytes; Humans; RNA, Messenger; Mitogen-Activated Protein Kinases

Hepatocyte apoptosis and stellate cell activation are both features of chronic liver diseases, but a relationship between these events has not been explored. In macrophages, engulfment of apoptotic bodies induces expression of transforming growth factor-beta (TGF-beta), a profibrogenic cytokine. We examined whether a similar response occurs in stellate cells. Fluorescently labeled hepatocyte apoptotic bodies were added to cultures of primary and immortalized human stellate cells. Stellate cells, but not hepatocytes, readily engulfed apoptotic bodies in a time-dependent manner as assessed by confocal microscopy. The activation of primary and immortalized human stellate cells after incubation with apoptotic bodies, as well as their fibrogenic activity, was indicated by an increase in alpha-smooth muscle actin (primary cells), TGF-beta1, and collagen alpha1(I) mRNA (primary and immortalized cells). The profibrogenic response was dependent upon apoptotic body engulfment, because nocodazole, a microtubule-inhibiting agent, blocked both the engulfment and the increase of TGF-beta1 and collagen alpha1(I) mRNA. As described in primary rodent stellate cells, up-regulation of collagen alpha1(I) mRNA was inhibited by a PI-3K inhibitor (LY294002) and a p38 mitogen-activated protein kinase inhibitor (SB203580) in LX-1 cells. In conclusion, these data support a model in which engulfment of hepatocyte apoptotic bodies by stellate cells leads to a fibrogenic response by eliciting a kinase-signaling pathway.