4.2 Article

Identification of Markers for Newly Formed β-Cells in the Perinatal Period: A Time of Recognized β-Cell Immaturity

Journal

JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
Volume 58, Issue 4, Pages 369-376

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1369/jhc.2009.954909

Keywords

islet cells; beta-cells; immunohistochemistry

Categories

Funding

  1. National Institutes of Health [DK-44523, DK-66056, DK-61251]
  2. Joslin Diabetes Endocrine Research Center [DK-36836]
  3. Juvenile Diabetes Research Foundation [JDRF 1-2004-120, 1-2000-389]
  4. Endocrine Fellow Foundation award
  5. Lawson-Wilkins Fellowship

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Markers of beta-cell maturity would be useful in staging the differentiation of stem/progenitor cells to beta-cells whether in vivo or in vitro. We previously identified markers for newly formed beta-cells in regenerating rat pancreases after 90% partial pancreatectomy. To test the generality of these markers of newly formed beta-cells, we examined their expression during the perinatal period, a time of recognized beta-cell immaturity. We show by semiquantitative RT-PCR and immunostaining over the time course from embryonic day 18/20 to birth, 1 day, 2 days, 3 days, 7 days, and adult that MMP-2, CK-19, and SPD are truly markers of new and immature beta-cells and that their expression transiently peaks in the perinatal period and is not entirely synchronous. The shared expression of these markers among fetal, newborn, and newly regenerated beta-cells, but not adult, strongly supports their use as potential markers for new beta-cells in the assessment of both the maturity of stem cell derived insulin-producing cells and the presence of newly formed islets (neogenesis) in the adult pancreas. (J Histochem Cytochem 58:369-376, 2010)

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