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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Current Stem Cell Research &amp; Therapy</journal-id><journal-title-group><journal-title xml:lang="en">Current Stem Cell Research &amp; Therapy</journal-title><trans-title-group xml:lang="ru"><trans-title>Current Stem Cell Research &amp; Therapy</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1574-888X</issn><issn publication-format="electronic">2212-3946</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">645579</article-id><article-id pub-id-type="doi">10.2174/011574888X267226231126185532</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Medicine</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Evaluation of Pancreatic β-cell Differentiation Efficiency of Human iPSC Lines for Clinical Use</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Horikawa</surname><given-names>Ayumi</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Tsuda</surname><given-names>Kyoko</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Yamamoto</surname><given-names>Takayoshi</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Michiue</surname><given-names>Tatsuo</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution>Department of Life Sciences (Biology), Graduate School of Arts and Sciences, University of Tokyo</institution></aff><pub-date date-type="pub" iso-8601-date="2024-11-01" publication-format="electronic"><day>01</day><month>11</month><year>2024</year></pub-date><volume>19</volume><issue>11</issue><issue-title xml:lang="ru"/><fpage>1449</fpage><lpage>1460</lpage><history><date date-type="received" iso-8601-date="2025-01-11"><day>11</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://journals.eco-vector.com/1574-888X/article/view/645579">https://journals.eco-vector.com/1574-888X/article/view/645579</self-uri><abstract xml:lang="en"><p id="idm46466589668624">Background:Transplantation of pancreatic β-cells generated from human induced pluripotent stem cells (hiPSCs) has great potential as a root treatment for type 1 diabetes. However, their current level of efficiency to differentiate into β-cells is still not at par for clinical use. Previous research has shown that differentiation efficiency varies among human embryonic stem cells and mouse-induced pluripotent stem cell lines. Therefore, selecting a suitable cell line for efficient induction into desired tissues and organs is crucial.</p><p id="idm46466589672624">Methods:In this study, we have evaluated the efficiency of 15 hiPSC lines available for clinical use to differentiate into pancreatic β-cells.</p><p id="idm46466589676592">Results:Our investigation has revealed induction efficiency to differ among the hiPSC lines, even when derived from the same donor. Among the hiPSC lines tested, the 16A01 cell line exhibited the highest insulin expression and low glucagon expression, suggesting that this cell line is suitable for differentiation into β-cells.</p><p id="idm46466589681648">Conclusion:Our study has demonstrated the importance of selecting a suitable hiPSC line for effective differentiation into β-cells.</p></abstract><kwd-group xml:lang="en"><kwd>iPS cells</kwd><kwd>β-cells</kwd><kwd>regenerative medicine</kwd><kwd>diabetes</kwd><kwd>insulin</kwd><kwd>stem cell</kwd><kwd>pancreas.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Foster, N.C.; Beck, R.W.; Miller, K.M.; Clements, M.A.; Rickels, M.R.; DiMeglio, L.A.; Maahs, D.M.; Tamborlane, W.V.; Bergenstal, R.; Smith, E.; Olson, B.A.; Garg, S.K. State of type 1 diabetes management and outcomes from the T1D exchange in 20162018. Diabetes Technol. 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