The pancreatic ductal epithelium serves as a potential pool of progenitor cells

被引:221
作者
Bonner-Weir, S [1 ]
Toschi, E [1 ]
Inada, A [1 ]
Reitz, P [1 ]
Fonseca, SY [1 ]
Aye, T [1 ]
Sharma, A [1 ]
机构
[1] Harvard Univ, Sch Med, Joslin Diabet Ctr, Dept Med,Res Div, Boston, MA 02215 USA
关键词
beta-cell growth; endocrine pancreas; pancreatic; progenitors;
D O I
10.1111/j.1399-543X.2004.00075.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
With the increasing success of islet transplantation, beta-cell replacement therapy has had renewed interest. To make such a therapy available to more than a few of the thousands of patients with diabetes, new sources of insulin-producing cells must become readily available. The most promising sources are stem cells, whether embryonic or adult stem cells. Clearly identifiable adult pancreatic stem cells have yet to be characterized. Although considerable evidence suggests their possibility, recent lineage-tracing experiments challenge their existence. Even in light of these lineage-tracing experiments, we suggest that evidence for neogenesis or new islet formation after birth remains strong. Our work has suggested that the pancreatic duct epithelium itself serves as a pool for progenitors for both islet and acinar tissues after birth and into adulthood and, thus, that the duct epithelium can be considered 'facultative stem cells'. We will develop our case for this hypothesis in this perspective.
引用
收藏
页码:16 / 22
页数:7
相关论文
共 48 条
[41]  
TOSCHI E, 2004, GENE EXPRESSION P S2, V53
[42]   Nestin-lineage cells contribute to the microvasculature but not endocrine cells of the islet [J].
Treutelaar, MK ;
Skidmore, JM ;
Dias-Leme, CL ;
Hara, M ;
Zhang, LZ ;
Simeone, D ;
Martin, DM ;
Burant, CF .
DIABETES, 2003, 52 (10) :2503-2512
[43]   REGULATION OF PANCREATIC DUCT EPITHELIAL GROWTH-INVITRO [J].
VERME, TB ;
HOOTMAN, SR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (06) :G833-G840
[44]   PANCREATIC GASTRIN STIMULATES ISLET DIFFERENTIATION OF TRANSFORMING GROWTH-FACTOR ALPHA-INDUCED DUCTULAR PRECURSOR CELLS [J].
WANG, TC ;
BONNERWEIR, S ;
OATES, PS ;
CHULAK, M ;
SIMON, B ;
MERLINO, GT ;
SCHMIDT, EV ;
BRAND, SJ .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (03) :1349-1356
[45]   Exendin-4 stimulates both β-cell replication and neogenesis, resulting in increased β-cell mass and improved glucose tolerance in diabetic rats [J].
Xu, G ;
Stoffers, DA ;
Habener, JF ;
Bonner-Weir, S .
DIABETES, 1999, 48 (12) :2270-2276
[46]   Recombinant human betacellulin promotes the neogenesis of β-cells and ameliorates glucose intolerance in mice with diabetes induced by selective alloxan perfusion [J].
Yamamoto, K ;
Miyagawa, J ;
Waguri, M ;
Sasada, R ;
Igarashi, K ;
Li, M ;
Nammo, T ;
Moriwaki, M ;
Imagawa, A ;
Yamagata, K ;
Nakajima, H ;
Namba, M ;
Tochino, Y ;
Hanafusa, T ;
Matsuzawa, Y .
DIABETES, 2000, 49 (12) :2021-2027
[47]   Selective β-cell loss and β-cell expansion in patients with type 2 diabetes mellitus in Korea [J].
Yoon, KH ;
Ko, SH ;
Cho, JH ;
Lee, JM ;
Ahn, YB ;
Song, KH ;
Yoo, SJ ;
Kang, MI ;
Cha, BY ;
Lee, KW ;
Son, HY ;
Kang, SK ;
Kim, HS ;
Lee, IK ;
Bonner-Weir, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (05) :2300-2308
[48]   Recovery of the endogenous β cell function in the NOD model of autoimmune diabetes [J].
Zorina, TD ;
Subbotin, VM ;
Bertera, S ;
Alexander, AM ;
Haluszczak, C ;
Gambrell, B ;
Bottino, R ;
Styche, AJ ;
Trucco, M .
STEM CELLS, 2003, 21 (04) :377-388