The Adult Mouse and Human Pancreas Contain Rare Multipotent Stem Cells that Express Insulin

被引:180
作者
Smukler, Simon R. [1 ]
Arntfield, Margot E. [1 ]
Razavi, Rozita [1 ]
Bikopoulos, George [2 ]
Karpowicz, Phillip [1 ]
Seaberg, Raewyn [1 ]
Dai, Feihan [2 ]
Lee, Simon [2 ]
Ahrens, Rosemary [3 ]
Fraser, Paul E. [3 ]
Wheeler, Michael B. [2 ]
van der Kooy, Derek [1 ,3 ]
机构
[1] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Med Biophys, Toronto, ON M5S 1A8, Canada
基金
加拿大健康研究院;
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; GREEN FLUORESCENT PROTEIN; BETA-CELLS; PROGENITOR CELLS; PRECURSOR CELLS; POSITIVE CELLS; NEURAL CREST; ISLET CELLS; IN-VITRO; PROLIFERATION;
D O I
10.1016/j.stem.2011.01.015
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The search for putative precursor cells within the pancreas has been the focus of extensive research. Previously, we identified rare pancreas-derived multipotent precursor (PMP) cells in the mouse with the intriguing capacity to generate progeny in the pancreatic and neural lineages. Here, we establish the embryonic pancreas as the developmental source of PMPs through lineage-labeling experiments. We also show that PMPs express insulin and can contribute to multiple pancreatic and neural cell types in vivo. In addition, we have isolated PMPs from adult human islet tissue that are also capable of extensive proliferation, self-renewal, and generation of multiple differentiated pancreatic and neural cell types. Finally, both mouse and human PMP-derived cells ameliorated diabetes in transplanted mice. These findings demonstrate that the adult Mammalian pancreas contains a population of insulin(+) multipotent stem cells and suggest that these cells may provide a promising line of investigation toward potential therapeutic benefit.
引用
收藏
页码:281 / 293
页数:13
相关论文
共 36 条
[1]   No evidence for mouse pancreatic β-cell epithelial-mesenchymal transition in vitro [J].
Atouf, Fouad ;
Park, Cheol Hong ;
Pechhold, Klaus ;
Ta, Malancha ;
Choi, Yong ;
Lumelsky, Nadya L. .
DIABETES, 2007, 56 (03) :699-702
[2]   All β cells contribute equally to islet growth and maintenance [J].
Brennand, Kristen ;
Huangfu, Danwei ;
Melton, Doug .
PLOS BIOLOGY, 2007, 5 (07) :1520-1529
[3]   Assessment of human pancreatic islet architecture and composition by laser scanning confocal microscopy [J].
Brissova, M ;
Fowler, MJ ;
Nicholson, WE ;
Chu, A ;
Hirshberg, B ;
Harlan, DM ;
Powers, AC .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2005, 53 (09) :1087-1097
[4]   Islet-derived fibroblast-like cells are not derived via epithelial-mesenchymal transition from Pdx-1 or insulin-positive cells [J].
Chase, Lucas G. ;
Ulloa-Montoya, Fernando ;
Kidder, Benjamin L. ;
Verfaillie, Catherine M. .
DIABETES, 2007, 56 (01) :3-7
[5]   Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase [J].
Danielian, PS ;
Muccino, D ;
Rowitch, DH ;
Michael, SK ;
McMahon, AP .
CURRENT BIOLOGY, 1998, 8 (24) :1323-1326
[6]   Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation [J].
Dor, Y ;
Brown, J ;
Martinez, OI ;
Melton, DA .
NATURE, 2004, 429 (6987) :41-46
[7]   Notch signalling suppresses apoptosis in adult human and mouse pancreatic islet cells [J].
Dror, V. ;
Nguyen, V. ;
Walia, P. ;
Kalynyak, T. B. ;
Hill, J. A. ;
Johnson, J. D. .
DIABETOLOGIA, 2007, 50 (12) :2504-2515
[8]  
Dupin E, 2006, ADV EXP MED BIOL, V589, P96
[9]  
ECHELARD Y, 1994, DEVELOPMENT, V120, P2213
[10]   A dermal niche for multipotent adult skin-derived precursor cells [J].
Fernandes, KJL ;
McKenzie, IA ;
Mill, P ;
Smith, KM ;
Akhavan, M ;
Barnabé-Heider, F ;
Biernaskie, J ;
Junek, A ;
Kobayashi, NR ;
Toma, JG ;
Kaplan, DR ;
Labosky, PA ;
Rafuse, V ;
Hui, CC ;
Miller, FD .
NATURE CELL BIOLOGY, 2004, 6 (11) :1082-U16