Differentiation of new insulin-producing cells is induced by injury in adult pancreatic islets

被引:190
作者
Fernandes, A
King, LC
Guz, Y
Stein, R
Wright, CVE
Teitelman, G
机构
[1] SUNY HLTH SCI CTR, DEPT ANAT & CELL BIOL, BROOKLYN, NY 11203 USA
[2] VANDERBILT UNIV, MED CTR, DEPT CELL BIOL, NASHVILLE, TN 37232 USA
[3] VANDERBILT UNIV, MED CTR, DEPT PHYSIOL & MOL BIOPHYS, NASHVILLE, TN 37232 USA
关键词
D O I
10.1210/en.138.4.1750
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The ability of the adult pancreas to generate new insulin (beta) cells has been controversial because of difficulties in unequivocally identifying the precursor population. We recently determined that beta cells were generated during development from precursors that expressed the homeodamain-containing transcription factor pancreas duodenum homeobox gene-1 (PDX-1). To investigate whether PDX-1(+) stem cells are present in adult pancreas, we examined two animal models of diabetes. One model was produced by injecting adult mice with streptozotocin (SZ), a toxin that produces hyperglycemia due to rapid and massive beta cell death. After SZ-mediated elimination of existing IN+/PDX-1(+) cells, a population of somatostatin (SOM)(+)/PDX-1(divided by) cells, a cell type thought to represent an embryonic islet precursor cell, appeared in islets. The appearance of SOM(+)/PDX-1(+) cells was followed in time by the differentiation to SOM(+)/IN+/PDX-1(+) cells. SOM (+)/PDX-1(+) cells also appeared in islets of nonobese diabetic mice, a strain of mice in which beta cell destruction is immune-mediated. Our findings establish the existence of PDX-1(+) beta cell precursors in the adult pancreas and indicate that their differentiation is induced by islet injury.
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页码:1750 / 1762
页数:13
相关论文
共 52 条
[1]
HYBRID INSULIN GENES REVEAL A DEVELOPMENTAL LINEAGE FOR PANCREATIC ENDOCRINE-CELLS AND IMPLY A RELATIONSHIP WITH NEURONS [J].
ALPERT, S ;
HANAHAN, D ;
TEITELMAN, G .
CELL, 1988, 53 (02) :295-308
[2]
[Anonymous], 1986, OPTICS
[3]
INSULITIS AND DIABETES IN NOD MICE REDUCED BY PROPHYLACTIC INSULIN THERAPY [J].
ATKINSON, MA ;
MACLAREN, NK ;
LUCHETTA, R .
DIABETES, 1990, 39 (08) :933-937
[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]
RESPONSES OF NEONATAL RAT ISLETS TO STREPTOZOTOCIN - LIMITED B-CELL REGENERATION AND HYPERGLYCEMIA [J].
BONNERWEIR, S ;
TRENT, DF ;
HONEY, RN ;
WEIR, GC .
DIABETES, 1981, 30 (01) :64-69
[7]
REGULATION OF ISLET BETA-CELL PROLIFERATION BY PROLACTIN IN RAT ISLETS [J].
BRELJE, TC ;
PARSONS, JA ;
SORENSON, RL .
DIABETES, 1994, 43 (02) :263-273
[8]
BRODSKY G, 1969, DIABETES, V18, P606
[9]
THE MIDGESTATIONAL HUMAN FETAL PANCREAS CONTAINS CELLS COEXPRESSING ISLET HORMONES [J].
DEKRIJGER, RR ;
AANSTOOT, HJ ;
KRANENBURG, G ;
REINHARD, M ;
VISSER, WJ ;
BRUINING, GJ .
DEVELOPMENTAL BIOLOGY, 1992, 153 (02) :368-375
[10]
ULTRASTRUCTURAL-STUDY OF PANCREATIC-B CELL REGENERATION IN NEWBORN RATS AFTER DESTRUCTION BY STREPTOZOTOCIN [J].
DUTRILLAUX, MC ;
PORTHA, B ;
ROZE, C ;
HOLLANDE, E .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1982, 39 (02) :173-185