Expression of islet-specific microRNAs during human pancreatic development

被引:198
作者
Joglekar, Mugdha V. [1 ]
Joglekar, Vinay M. [2 ]
Hardikar, Anandwardhan A. [1 ]
机构
[1] Natl Ctr Cell Sci, Stem Cells & Diabet Sect, Lab 12, Pune 411007, Maharashtra, India
[2] Shree Seva Med Fdn, Satara 412801, Maharashtra, India
关键词
Human pancreas development; Islet; microRNA; miR-375; miR-7; Insulin; Diabetes; HUMAN-FETAL PANCREAS; ZEBRAFISH; CELLS;
D O I
10.1016/j.gep.2008.10.001
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
During pancreatic islet development, sequential changes in gene expression are known to be necessary for efficient differentiation and function of the endocrine pancreas. Several studies till now have demonstrated that microRNAs (miRNAs), which regulate translation of gene transcripts, influence gene expression cascades involved in pancreas development. Some of these miRNAs: miR-7 and miR-375 have been known to be expressed at high levels in pancreas and are also known to be involved in Zebrafish pancreas development as well as insulin secretion in mice. We demonstrate here that 4 different islet-specific microRNAs (miR-7, miR-9, miR-375 and miR-376) are expressed at high levels during human pancreatic islet development. Of these, miR-375, is seen to be differentially expressed in human islet beta- as well as non-beta-cells. Though no significant difference in abundance of miR-375 was noted in either cell type, analysis of islet-specific miRNA and mRNA in single cells show that non-p cells contain higher levels of miR-375. Our data demonstrate that miRNAs that are known to be regulated during Zebrafish pancreatic development may play similar role in human pancreatic islet development. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 113
页数:5
相关论文
共 17 条
[1]
Quantitative differential expression analysis reveals miR-7 as major islet microRNA [J].
Bravo-Egana, Valia ;
Rosero, Samuel ;
Molano, R. Damaris ;
Pileggi, Antonello ;
Ricordi, Camillo ;
Dominguez-Bendala, Juan ;
Pastori, Ricardo L. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 366 (04) :922-926
[2]
Epithelial-to-mesenchymal transition generates proliferative human islet precursor cells [J].
Gershengorn, MC ;
Hardikar, AA ;
Wei, CJ ;
Geras-Raaka, E ;
Marcus-Samuels, B ;
Raaka, BM .
SCIENCE, 2004, 306 (5705) :2261-2264
[3]
New pancreas from old: microregulators of pancreas regeneration [J].
Joglekar, Mugdha V. ;
Parekh, Vishal S. ;
Hardikar, Anandwardhan A. .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2007, 18 (10) :393-400
[4]
MicroRNA profiling of developing and regenerating pancreas reveal post-transcriptional regulation of neurogenin3 [J].
Joglekar, Mugdha V. ;
Parekh, Vishal S. ;
Mehta, Sameet ;
Bhonde, Ramesh R. ;
Hardikar, Anandwardhan A. .
DEVELOPMENTAL BIOLOGY, 2007, 311 (02) :603-612
[5]
Targeted inhibition of miRNA maturation with morpholinos reveals a role for miR-375 in pancreatic islet development (Publication with Expression of Concern. See vol. 20, 2022) [J].
Kloosterman, Wigard P. ;
Lagendijk, Anne K. ;
Ketting, Rene F. ;
Moulton, Jon D. ;
Plasterk, Ronald H. A. .
PLOS BIOLOGY, 2007, 5 (08) :1738-1749
[6]
DEVELOPMENT OF A METHOD FOR ISOLATION OF ISLETS FROM HUMAN-FETAL PANCREAS [J].
KOVER, K ;
MOORE, WV .
DIABETES, 1989, 38 (07) :917-924
[7]
MicroRNA expression is required for pancreatic islet cell genesis in the mouse [J].
Lynn, Francis C. ;
Skewes-Cox, Peter ;
Kosaka, Yasuhiro ;
McManus, Michael T. ;
Harfe, Brian D. ;
German, Michael S. .
DIABETES, 2007, 56 (12) :2938-2945
[8]
Transcription factor expression in the developing human fetal endocrine pancreas [J].
Lyttle, B. M. ;
Krishnamurthy, J. Li M. ;
Fellows, F. ;
Wheeler, M. B. ;
Goodyer, C. G. ;
Wang, R. .
DIABETOLOGIA, 2008, 51 (07) :1169-1180
[9]
From endoderm formation to liver and pancreas development in zebrafish [J].
Ober, EA ;
Field, HA ;
Stainier, DYR .
MECHANISMS OF DEVELOPMENT, 2003, 120 (01) :5-18
[10]
A new mathematical model for relative quantification in real-time RT-PCR [J].
Pfaffl, MW .
NUCLEIC ACIDS RESEARCH, 2001, 29 (09) :E45