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<XML><RECORDS>
<RECORD>
	<REFERENCE_TYPE>31</REFERENCE_TYPE>
	<AUTHORS>
		<AUTHOR>Kikugawa, R.</AUTHOR>
		<AUTHOR>Katsuta, H.</AUTHOR>
		<AUTHOR>Akashi, T.</AUTHOR>
		<AUTHOR>Yatoh, S.</AUTHOR>
		<AUTHOR>Weir, G. C.</AUTHOR>
		<AUTHOR>Sharma, A.</AUTHOR>
		<AUTHOR>Bonner-Weir, S.</AUTHOR>
	</AUTHORS>
	<YEAR>2009</YEAR>
	<TITLE>Differentiation of COPAS-sorted non-endocrine pancreatic cells into insulin-positive cells in the mouse</TITLE>
	<SECONDARY_TITLE>Diabetologia</SECONDARY_TITLE>
	<DATE>Jan 30</DATE>
	<ISBN>1432-0428 (Electronic)</ISBN>
	<ACCESSION_NUMBER>19183938</ACCESSION_NUMBER>
	<ABSTRACT>AIMS/HYPOTHESIS: The regenerative process in the pancreas is of particular interest, since insulin-producing beta cells are lost in diabetes. Differentiation of new beta cells from pancreatic non-endocrine cells has been reported in vivo and in vitro, a finding that implies the existence of pancreatic stem/progenitor cells. However, while tissue-specific stem cells are well documented in skin, intestine and testis, pancreatic stem cells have been elusive. We hypothesised that pancreatic stem/progenitor cells within the non-endocrine fraction could be a source of new islets in vitro. METHODS: To test if there were such cells within the pancreas, we generated pancreatic cell aggregates from tissue remaining after islet isolation from mouse insulin promoter 1-green fluorescent protein (MIP-GFP) mice. To eliminate any contamination of insulin-positive cells, we deleted all GFP-positive aggregates using COPAS Select and cultured with Matrigel. Immunohistochemistry, quantitative real-time PCR and single-cell nested RT-PCR were performed to confirm formation of insulin-producing cells. RESULTS: The GFP-negative cells were expanded as monolayers and then differentiated into three-dimensional cystic structures. After 1 week of culture, GFP-positive cells were found as clusters or single cells. By quantitative real-time PCR, no insulin mRNA was detected immediately after COPAS sorting, but after differentiation insulin mRNA of the whole preparation was 1.91 +/- 0.31% that of purified MIP-GFP beta cells. All GFP-positive cells expressed insulin 1; most expressed insulin 2, pancreas duodenum homeobox-1 and cytokeratin 19 by single cell nested RT-PCR. CONCLUSIONS/INTERPRETATION: Our data support the concept that within the exocrine (acinar and ductal) pancreas of the adult mouse there are cells that can give rise to insulin-positive cells in vitro.</ABSTRACT>
	<NOTES>Journal article</NOTES>
	<URL>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=PubMed&amp;dopt=Citation&amp;list_uids=19183938</URL>
</RECORD>
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