Deconstructing Pancreas Developmental Biology

被引:52
作者
Benitez, Cecil M. [1 ]
Goodyer, William R. [1 ]
Kim, Seung K. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Med, Div Oncol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
SECRETORY GRANULE BIOGENESIS; ALPHA-CELL-DIFFERENTIATION; ISLET BETA-CELL; HISTONE METHYLTRANSFERASE COMPLEX; ENDOCRINE PANCREAS; INSULIN-SECRETION; TRANSCRIPTION FACTOR; CHROMOGRANIN-A; ACINAR-CELL; GLUCOSE-METABOLISM;
D O I
10.1101/cshperspect.a012401
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The relentless nature and increasing prevalence of human pancreatic diseases, in particular, diabetes mellitus and adenocarcinoma, has motivated further understanding of pancreas organogenesis. The pancreas is a multifunctional organ whose epithelial cells govern a diversity of physiologically vital endocrine and exocrine functions. The mechanisms governing the birth, differentiation, morphogenesis, growth, maturation, and maintenance of the endocrine and exocrine components in the pancreas have been discovered recently with increasing tempo. This includes recent studies unveiling mechanisms permitting unexpected flexibility in the developmental potential of immature and mature pancreatic cell subsets, including the ability to interconvert fates. In this article, we describe how classical cell biology, genetic analysis, lineage tracing, and embryological investigations are being complemented by powerful modern methods including epigenetic analysis, time-lapse imaging, and flow cytometry-based cell purification to dissect fundamental processes of pancreas development.
引用
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页数:17
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