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
相关论文
共 23 条
[1]   MafB is required for islet β cell maturation [J].
Artner, Isabella ;
Bianchi, Bruno ;
Raum, Jeffrey C. ;
Guo, Min ;
Kaneko, Tomomi ;
Cordes, Sabine ;
Sieweke, Michael ;
Stein, Roland .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (10) :3853-3858
[2]   GLUCOSE-INDUCED INSULIN RELEASE IN ISLETS OF YOUNG-RATS - TIME-DEPENDENT POTENTIATION AND EFFECTS OF 2-BROMOSTEARATE [J].
BLISS, CR ;
SHARP, GWG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (05) :E890-E896
[3]  
Bonner-Weir Susan, 1997, P138
[4]   PARTIAL PANCREATECTOMY IN THE RAT AND SUBSEQUENT DEFECT IN GLUCOSE-INDUCED INSULIN RELEASE [J].
BONNERWEIR, S ;
TRENT, DF ;
WEIR, GC .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 71 (06) :1544-1553
[5]   A 2ND PATHWAY FOR REGENERATION OF ADULT EXOCRINE AND ENDOCRINE PANCREAS - A POSSIBLE RECAPITULATION OF EMBRYONIC-DEVELOPMENT [J].
BONNERWEIR, S ;
BAXTER, LA ;
SCHUPPIN, GT ;
SMITH, FE .
DIABETES, 1993, 42 (12) :1715-1720
[6]   HETEROGENEOUS SECRETION OF INDIVIDUAL B-CELLS IN RESPONSE TO D-GLUCOSE AND TO NONGLUCIDIC NUTRIENT SECRETAGOGUES [J].
BOSCO, D ;
MEDA, P ;
THORENS, B ;
MALAISSE, WJ .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 268 (03) :C611-C618
[7]   Proliferation and differentiation in the human fetal endocrine pancreas [J].
Bouwens, L ;
Lu, WG ;
DeKrijger, R .
DIABETOLOGIA, 1997, 40 (04) :398-404
[8]   CYTOKERATINS AS MARKERS OF DUCTAL CELL-DIFFERENTIATION AND ISLET NEOGENESIS IN THE NEONATAL RAT PANCREAS [J].
BOUWENS, L ;
WANG, RN ;
DEBLAY, E ;
PIPELEERS, DG ;
KLOPPEL, G .
DIABETES, 1994, 43 (11) :1279-1283
[9]   FUNCTIONAL MATURATION AND PROLIFERATION OF FETAL PANCREATIC BETA-CELLS [J].
HELLERSTROM, C ;
SWENNE, I .
DIABETES, 1991, 40 :89-93
[10]   Carbonic anhydrase II-positive pancreatic cells are progenitors for both endocrine and exocrine pancreas after birth [J].
Inada, Akari ;
Nienaber, Cameron ;
Katsuta, Hitoshi ;
Fujitani, Yoshio ;
Levine, Jared ;
Morita, Rina ;
Sharma, Arun ;
Bonner-Weir, Susan .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (50) :19915-19919