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

被引:36
作者
Aye, Tandy [1 ]
Toschi, Elena [1 ]
Sharma, Arun [1 ]
Sgroi, Dennis [2 ]
Bonner-Weir, Susan [1 ]
机构
[1] Joslin Diabets Ctr, Sect Islet Transplantat & Cell Biol, Boston, MA 02215 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Pathol, Boston, MA USA
基金
美国国家卫生研究院;
关键词
islet cells; beta-cells; immunohistochemistry; INDUCED INSULIN RELEASE; ENDOCRINE PANCREAS; HUMAN FETAL; DIFFERENTIATION; PROLIFERATION; GLUCOSE; RAT; REGENERATION; EXPRESSION; MATURATION;
D O I
10.1369/jhc.2009.954909
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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)
引用
收藏
页码:369 / 376
页数:8
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