Formation of insulin-producing cells from pancreatic acinar AR42J cells by hepatocyte growth factor

H Mashima, H Shibata, T Mine, I Kojima - Endocrinology, 1996 - academic.oup.com
H Mashima, H Shibata, T Mine, I Kojima
Endocrinology, 1996academic.oup.com
Pancreatic AR42J cells are derived from acinar cells and express both exocrine and
neuroendocrine properties. We have recently shown that these cells convert into insulin-
producing cells in vitro after treatment with activin A and betacellulin. Here, we investigated
the effect of hepatocyte growth factor (HGF) in those cells. When AR42J cells were
incubated with HGF, DNA synthesis was attenuated, and the amylase content was reduced
in a concentration-dependent manner. HGF-treated cells extended processes, but bundle …
Abstract
Pancreatic AR42J cells are derived from acinar cells and express both exocrine and neuroendocrine properties. We have recently shown that these cells convert into insulin-producing cells in vitro after treatment with activin A and betacellulin. Here, we investigated the effect of hepatocyte growth factor (HGF) in those cells. When AR42J cells were incubated with HGF, DNA synthesis was attenuated, and the amylase content was reduced in a concentration-dependent manner. HGF-treated cells extended processes, but bundle formation was not observed using an antibody against tubulin. Reverse both insulin and pancreatic polypeptide (PP) were expressed in HGF-treated, but not naive, AR42J cells. Immunocytochemical analysis indicated that approximately 3% of the HGF-treated cells were stained with antiinsulin antibody, and some were also stained with anti-PP antibody. When AR42J cells were exposed to a combination of activin A and HGF, cells extended longer processes, and over 10% of them were stained with antiinsulin antibody. In these cells, messenger RNAs for insulin, PP, glucose transporter 2, and glucokinase, but not those for glucagon or somatostatin, were expressed. A subclone of AR42J cells, AR42J-B13, was obtained. Most of the AR42J-B13 cells converted to insulin-producing cells after the incubation with activin A and HGF. Insulin secretion was augmented by tolbutamide, depolarizing concentrations of potassium, carbachol, and glucagon-like peptide-1 in these cells. These results indicate that HGF reduces the acinar cell-like property of AR42J cells and converts them into insulin-producing cells. The effect of HGF was markedly enhanced by activin A.
Oxford University Press