| Literature DB >> 12606518 |
Tomoaki Morioka1, Hidenori Koyama, Hisako Yamamura, Shinji Tanaka, Shinya Fukumoto, Masanori Emoto, Hiroyuki Mizuguchi, Takao Hayakawa, Itaru Kojima, Katsuhito Takahashi, Yoshiki Nishizawa.
Abstract
Basic or h1-calponin is a smooth muscle-specific, actin-binding protein that is involved in the regulation of smooth muscle contractile activity. We found in this study the expression of mRNA and protein for h1-calponin in AR42J-B13 cells, which is a useful model for investigating islet beta-cell differentiation from pancreatic common precursor cells. Following treatment of AR42J cells with activin A and hepatocyte growth factor, the protein levels of h1-calponin decreased in a time-dependent manner during the course of the cell differentiation. When h1-calponin was continuously overexpressed by utilizing recombinant adenovirus-mediated gene transfer, the percentage of cell differentiation in h1-calponin overexpressing cells was markedly suppressed as compared with that in the cells without overexpression (6.7 +/- 2.5 vs. 28.6 +/- 3.2%, P < 0.001, Student's t test). Finally, overexpression of h1-calponin (65.6 +/- 3.4), or that lacking actin-binding domain (55.9 +/- 3.4%), significantly (P < 0.001) suppressed the activin A-stimulated transcriptional activity of activin responsive element (ARE), whereas calponin homology-domain disruption mutant did not (100.6 +/- 1.9%). These results suggest that regulation of h1-calponin is involved in the regulation of differentiation of AR42J cells into insulin-producing cells at least partly through modulating ARE transcriptional activity.Entities:
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Year: 2003 PMID: 12606518 DOI: 10.2337/diabetes.52.3.760
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461