Pancreas Organogenesis: From Bud to Plexus to Gland

被引:452
作者
Pan, Fong Cheng
Wright, Chris [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Cell & Dev Biol, Nashville, TN 37232 USA
关键词
pancreas organogenesis; patterning; tubulogenesis; tip-trunk compartmentalization; plexus remodeling; branching morphogenesis; endocrine specification and differentiation; exocrine development; human pancreas; reprogramming; ISLET BETA-CELL; NUCLEAR FACTOR 3-BETA; EMBRYONIC STEM-CELLS; STIMULATED INSULIN-SECRETION; TRANSCRIPTION FACTOR MIST1; FIBROBLAST GROWTH-FACTORS; DEVELOPING MOUSE PANCREAS; HOMEODOMAIN PROTEIN PDX1; LOOP-HELIX COMPLEX; HOMEOBOX GENE HEX;
D O I
10.1002/dvdy.22584
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Pancreas oganogenesis comprises a coordinated and highly complex interplay of signaling events and transcriptional networks that guide a step-wise process of organ development from early bud specification all the way to the final mature organ state. Extensive research on pancreas development over the last few years, largely driven by a translational potential for pancreatic diseases (diabetes, pancreatic cancer, and so on), is markedly advancing our knowledge of these processes. It is a tenable goal that we will one day have a clear, complete picture of the transcriptional and signaling codes that control the entire organogenetic process, allowing us to apply this knowledge in a therapeutic context, by generating replacement cells in vitro, or perhaps one day to the whole organ in vivo. This review summarizes findings in the past 5 years that we feel are amongst the most significant in contributing to the deeper understanding of pancreas development. Rather than try to cover all aspects comprehensively, we have chosen to highlight interesting new concepts, and to discuss provocatively some of the more controversial findings or proposals. At the end of the review, we include a perspective section on how the whole pancreas differentiation process might be able to be unwound in a regulated fashion, or redirected, and suggest linkages to the possible reprogramming of other pancreatic cell-types in vivo, and to the optimization of the forward-directed-differentiation of human embryonic stem cells (hESC), or induced pluripotential cells (iPSC), towards mature beta-cells. Developmental Dynamics 240:530-565, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:530 / 565
页数:36
相关论文
共 288 条
[1]   Molecular regulation of pancreatic β-cell mass development, maintenance, and expansion [J].
Ackermann, Amanda M. ;
Gannon, Maureen .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2007, 38 (1-2) :193-206
[2]   DEVELOPMENT OF THE HUMAN-PANCREAS - VARIATIONS AND PATHOLOGY - A TENTATIVE CLASSIFICATION [J].
ADDA, G ;
HANNOUN, L ;
LOYGUE, J .
ANATOMIA CLINICA, 1984, 5 (04) :275-283
[3]   Combined ectopic expression of Pdx1 and Ptf1a/p48 results in the stable conversion of posterior endoderm into endocrine and exocrine pancreatic tissue [J].
Afelik, Solomon ;
Chen, Yonglong ;
Pieler, Tomas .
GENES & DEVELOPMENT, 2006, 20 (11) :1441-1446
[4]  
Ahlgren U, 1996, DEVELOPMENT, V122, P1409
[5]   Independent requirement for ISL1 in formation of pancreatic mesenchyme and islet cells [J].
Ahlgren, U ;
Pfaff, SL ;
Jessell, TM ;
Edlund, T ;
Edlund, H .
NATURE, 1997, 385 (6613) :257-260
[6]   β-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the β-cell phenotype and maturity onset diabetes [J].
Ahlgren, U ;
Jonsson, J ;
Jonsson, L ;
Simu, K ;
Edlund, H .
GENES & DEVELOPMENT, 1998, 12 (12) :1763-1768
[7]   Mesenchymal Bone Morphogenetic Protein Signaling Is Required for Normal Pancreas Development [J].
Ahnfelt-Ronne, Jonas ;
Ravassard, Philippe ;
Pardanaud-Glavieux, Corinne ;
Scharfmann, Raphael ;
Serup, Palle .
DIABETES, 2010, 59 (08) :1948-1956
[8]   Osteo-chondroprogenitor cells are derived from Sox9 expressing precursors [J].
Akiyama, H ;
Kim, JE ;
Nakashima, K ;
Balmes, G ;
Iwai, N ;
Deng, JM ;
Zhang, ZP ;
Martin, JF ;
Behringer, RR ;
Nakamura, T ;
de Crombrugghe, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (41) :14665-14670
[9]   Dre recombinase, like Cre, is a highly efficient site-specific recombinase in E-coli, mammalian cells and mice [J].
Anastassiadis, Konstantinos ;
Fu, Jun ;
Patsch, Christoph ;
Hu, Shengbiao ;
Weidlich, Stefanie ;
Duerschke, Kristin ;
Buchholz, Frank ;
Edenhofer, Frank ;
Stewart, A. Francis .
DISEASE MODELS & MECHANISMS, 2009, 2 (9-10) :508-515
[10]   Notch signalling controls pancreatic cell differentiation [J].
Apelqvist, Å ;
Li, H ;
Sommer, L ;
Beatus, P ;
Anderson, DJ ;
Honjo, T ;
de Angelis, MH ;
Lendahl, U ;
Edlund, H .
NATURE, 1999, 400 (6747) :877-881