2007
DOI: 10.1111/j.1872-034x.2007.00237.x
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Human intrahepatic biliary epithelial cell as a possible modulator of hepatic regeneration: Potential role of biliary epithelial cell for hepatic remodeling in vivo

Abstract: Considering that some of these factors had been already reported to have direct autocrine mitogenic influence on HIBEC, these findings could further strengthen an active role of HIBEC as a modulator of hepatic regeneration, through its biological reactivity on inflamed milieu.

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Cited by 12 publications
(7 citation statements)
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References 14 publications
(15 reference statements)
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“…In fact, IL-6 together with TNF␣ is responsible for a hepatocyte entering to the state of replication competence [41]. It has been demonstrated that IL-6, IL-8, and MCP-1 are produced by human intrahepatic biliary epithelial cells through toll-like receptor 4, nuclear factor-kappa B, and mitogen activated protein kinase signaling pathways, and therefore are possibly mediating an innate immune system function and modulating hepatic regeneration in vivo [42,43]. Then in the proliferation phase, HGF and TGF␣ stimulate proliferation of hepatocytes.…”
Section: Resultsmentioning
confidence: 99%
“…In fact, IL-6 together with TNF␣ is responsible for a hepatocyte entering to the state of replication competence [41]. It has been demonstrated that IL-6, IL-8, and MCP-1 are produced by human intrahepatic biliary epithelial cells through toll-like receptor 4, nuclear factor-kappa B, and mitogen activated protein kinase signaling pathways, and therefore are possibly mediating an innate immune system function and modulating hepatic regeneration in vivo [42,43]. Then in the proliferation phase, HGF and TGF␣ stimulate proliferation of hepatocytes.…”
Section: Resultsmentioning
confidence: 99%
“…147 In this context, it should be noted that the biliary epithelium can release IL-8, GROa, and ENA-78. 148,149 Based on these properties, a possible role of CXCR1 and/or CXCR2 inflammatory alterations of the biliary tract can be vividly envisioned. Moreover, it might also be relevant to consider that CXCR1 and CXCR2 have a role in the propagation of malignant processes, 146,150,151 which could be particularly relevant for cholangiocellular carcinomas arising in PSC patients.…”
Section: Chromosome 2q35mentioning
confidence: 99%
“…We reported that unstimulated conditioned medium of human cholangiocytes in vitro were already rich in multiple humoral factors, including ELR+CXC chemokines, such as IL-8/CXCL8, growth-related oncoprotein (GRO), epithelial neutrophil chemoattractant (ENA-78), known chemoattractants with wide range of non-leukocytic activities [27]. Moreover, human cholangiocytes were found to be permissive in TLR2, 4 and 3 dependent pathways in vitro, the former of which caused increase in the secretion of IL-6, monocyte chemotactic protein-1 (MCP-1), and IL-8, upon activation with LPS or LTA, respectively [72].…”
Section: Biliary Epithelial Cellsmentioning
confidence: 99%
“…BECs are one of the sources of chemokines, and BECs spontaneously produce GRO-α/CXCL1, ENA-78/CXCL5, GCP-2/CXCL6, IL-8/CXCL8 ( Figure 5) [27,60]. Fractalkine (CX3CL1), consisting of a membrane-bound form and a soluble chemotactic form, is produced by several epithelial cells and is associated with cell adhesion and the chemoattractant for its receptor (CX3CR1)-expressing cells such as CD8+ and CD4+T cells.…”
Section: Biliary Epithelial Cells In Immunological Inflammationmentioning
confidence: 99%