Редактирование: ANGPTL4

Angiopoietin-related protein 4 precursor (Angiopoietin-like protein 4) (Hepatic fibrinogen/angiopoietin-related protein) (HFARP) [Contains: ANGPTL4 N-terminal chain; ANGPTL4 C-terminal chain] [ARP4] [HFARP] [PGAR] [PP1158] [PSEC0166] [UNQ171/PRO197]

==Publications==

{{medline-entry
|title=Involvement of ERK1/2 activation in the gene expression of senescence-associated secretory factors in human hepatic stellate cells.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30426301
|abstract=Senescent hepatic stellate cells (senescent HSCs) are found in patients with liver cirrhosis and have been thought to be involved in the development of hepatocellular carcinoma (HCC) in mice via the senescence-associated secretory proteins. However, in humans, which secretory proteins are involved and what regulate their expression remain unclear. In the current study, we characterized senescence-associated β-galactosidase-positive senescent human HSCs (hHSCs) induced by repetitive passaging. They exhibited enhanced expression of 14 genes for secretory protein and persistent phosphorylation of ERK1/2 protein but not JNK or p38 MAPK proteins. Enhanced nuclear ERK1/2 phosphorylation was observed in senescent hHSCs. Treatment of the senescent hHSCs with ERK1/2 inhibitor, SCH772984, significantly decreased the levels of angiopoietin like 4 ([[ANGPTL4]]), C-C motif chemokine ligand 7 (CCL7), Interleukin-8 (IL-8), platelet factor 4 variant 1 ([[PF4V1]]), and [[TNF]] superfamily member 15 ([[TNF]]SF15) mRNA levels in a dose-dependent manner. The enhanced phosphorylation of ERK1/2 and expression of [[ANGPTL4]], IL-8 and [[PF4V1]] genes were observed in both of senescent human dermal fibroblasts and X-ray-induced senescent hHSCs. However, transient ERK1/2 activation induced by epidermal growth factor could not mimic the gene profile of the senescent hHSCs. These results revealed involvement of ERK1/2 signaling in the regulation of senescence-associated secretory factors, suggesting that simultaneous induction of [[ANGPTL4]], IL-8, and [[PF4V1]] genes is a marker of hHSC senescence. This study will contribute to understanding roles of senescent hHSCs in liver diseases.
|mesh-terms=* Cell Line
* Cellular Senescence
* Enzyme Activation
* Gene Expression Regulation
* Hepatic Stellate Cells
* Humans
* MAP Kinase Signaling System
* Mitogen-Activated Protein Kinase 1
* Mitogen-Activated Protein Kinase 3
|keywords=* ERK1/2
* Fibroblast
* Hepatic stellate cell
* Secretory factor
* Senescence
|full-text-url=https://sci-hub.do/10.1007/s11010-018-3466-x
}}