We first performed in vivo studies in BDL mice to demonstrate the decrease of large IBDM and de novo proliferation of small ducts after GABA in vivo administration. Small and large cholangiocytes differentially respond to liver injury with changes in apoptotic, proliferative, and secretory activities.5, 10, 25 After BDL, only large cholangiocytes proliferate, leading to increased IBDM and secretin-stimulated choleresis by activation of cAMP signaling.5, 10 After damage of large ducts by CCl4, small cholangiocytes (resistant to CCl4-induced apoptosis) de novo proliferate selleckchem and acquire large cholangiocyte phenotypes to compensate for the loss of large duct
functions.10 The mechanisms by which small cholangiocytes acquire phenotypes of large cholangiocytes are unknown. The differential apoptotic and proliferative responses to GABA in vitro treatment does not depend on selleck products the different expression of GABA receptors, because both small and large cholangiocytes express the three GABA receptors that likely mediate these effects. Indeed, our recent study20 in human cholangiocarcinoma
cells has shown that blocking of GABAA, GABAB, and GABAC receptors prevents GABA inhibition of cholangiocarcinoma proliferation. The reason why GABA damages only large ducts may also be the result of sensitization from obstructive cholestasis and subsequent biliary/seric accumulation26 as well as dysregulation of GABA metabolism during liver damage.27 The higher resistance of small cholangiocytes to GABA may also depend on their more undifferentiated nature,
whereas large (more differentiated) cholangiocytes are more susceptible to injury.11 Indeed, the presence of a larger nucleus and a smaller cytoplasm in small cholangiocytes suggests the undifferentiated nature of these cells.28 Large cholangiocytes (displaying a larger cytoplasm) are perhaps more differentiated cells and more susceptible to damage.28 The higher expression of the antiapoptotic protein, B-cell lymphoma 2, by small ducts in normal and cirrhotic human liver may also explain the higher resistance of small cholangiocytes to injury.29 The higher expression of Ca2+-dependent signaling may contribute to the higher resistance of the small cholangiocyte MCE公司 compartment to injury, as suggested in other cell systems.30 We propose several speculations to explain why small cholangiocytes differentiate in vivo into large cholangiocytes when the latter cells are damaged. During damage of large ducts, there must be a compensatory mechanism in the biliary epithelium (represented by small bile duct compartment) that is activated (acquiring traits of large cholangiocytes)10, 31 to maintain the homeostasis of the biliary tree. Also, the differentiation of small, undifferentiated cholangiocytes into large (more senescent) cholangiocytes may be a natural process of senescence accelerated by GABA.