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dc.contributor.authorKanafi, M.
dc.contributor.authorMamidi, M.
dc.contributor.authorSureshbabu, S.
dc.contributor.authorShahani, P.
dc.contributor.authorBhawna, C.
dc.contributor.authorWarrier, Sudha
dc.contributor.authorBhonde, R.
dc.date.accessioned2017-01-30T12:59:18Z
dc.date.available2017-01-30T12:59:18Z
dc.date.created2015-10-29T04:10:01Z
dc.date.issued2014
dc.identifier.citationKanafi, M. and Mamidi, M. and Sureshbabu, S. and Shahani, P. and Bhawna, C. and Warrier, S. and Bhonde, R. 2014. Generation of islet-like cell aggregates from human non-pancreatic cancer cell lines. Biotechnology Letters. 37 (1): pp. 227-233.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/27481
dc.identifier.doi10.1007/s10529-014-1662-7
dc.description.abstract

To explore a novel source for the derivation of islets, we examined the differentiation potential of human non-pancreatic cancer cell lines, HeLa (cervical carcinoma cell line) and MCF-7 (breast cancer cell line). These cells were subjected to a serum-free, three-step sequential differentiation protocol which gave two distinct cell populations: single cells and cellular aggregates. Subsequent analysis confirmed their identity as pancreatic acinar cells and islet-like cell aggregates (ICAs), as evidenced by amylase secretion and diphenylthiocarbazone staining respectively. Reverse transcriptase-PCR and immunocytochemistry assessment of the ICAs revealed the expression of pancreatic specific markers Ngn-3, Glut-2, Pax-6 and Isl-1. These ICAs secreted insulin in response to glucose challenge, confirming their functionality. We propose that ICAs generated from HeLa and MCF-7 cell lines could form a promising in vitro platform of human islet equivalents (hIEQs) for diabetes research.

dc.publisherKluwer Academic Publishers
dc.titleGeneration of islet-like cell aggregates from human non-pancreatic cancer cell lines
dc.typeJournal Article
dcterms.source.issn0141-5492
dcterms.source.titleBiotechnology Letters
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusFulltext not available


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