Persistent expression of PDX-1 in the pancreas causes acinar-to-ductal metaplasia through Stat3 activation

The transcription factor pancreatic and duodenal homeobox factor 1 (PDX-1) is expressed in pancreatic progenitor cells. In exocrine pancreas, PDX-1 is down-regulated during late development, while re-up-regulation of PDX-1 has been reported in pancreatic cancer and pancreatitis. To determine whether...

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Veröffentlicht in:Genes & development 2006-06, Vol.20 (11), p.1435-1440
Hauptverfasser: Miyatsuka, Takeshi, Kaneto, Hideaki, Shiraiwa, Toshihiko, Matsuoka, Taka-aki, Yamamoto, Kaoru, Kato, Ken, Nakamura, Yumiko, Akira, Shizuo, Takeda, Kiyoshi, Kajimoto, Yoshitaka, Yamasaki, Yoshimitsu, Sandgren, Eric P, Kawaguchi, Yoshiya, Wright, Christopher V E, Fujitani, Yoshio
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Sprache:eng
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Zusammenfassung:The transcription factor pancreatic and duodenal homeobox factor 1 (PDX-1) is expressed in pancreatic progenitor cells. In exocrine pancreas, PDX-1 is down-regulated during late development, while re-up-regulation of PDX-1 has been reported in pancreatic cancer and pancreatitis. To determine whether sustained expression of PDX-1 could affect pancreas development, PDX-1 was constitutively expressed in all pancreatic lineages by transgenic approaches. The transgenic pancreas was markedly small with the replacement of acinar cells by duct-like structures, accompanied by activated Stat3. Genetic ablation of Stat3 in the transgenic pancreas profoundly suppressed the metaplastic phenotype. These results provide a mechanism of pancreatic metaplasia by which persistent PDX-1 expression cell-autonomously induces acinar-to-ductal transition through Stat3 activation.
ISSN:0890-9369
1549-5477
DOI:10.1101/gad.1412806