Molecular properties of adult mouse gastric and intestinal epithelial progenitors in their niches

被引:137
作者
Giannakis, M
Stappenbeck, TS
Mills, JC
Leip, DG
Lovett, M
Clifton, SW
Ippolito, JE
Glasscock, JI
Arumugam, M
Brent, MR
Gordon, JI
机构
[1] Washington Univ, Ctr Genome Sci, St Louis, MO 63108 USA
[2] Washington Univ, Dept Mol Biol & Pharmacol, St Louis, MO 63108 USA
[3] Washington Univ, Dept Pathol & Immunol, St Louis, MO 63108 USA
[4] Washington Univ, Dept Genet, St Louis, MO 63108 USA
[5] Washington Univ, Lab Computat Genom, St Louis, MO 63108 USA
关键词
D O I
10.1074/jbc.M512118200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have sequenced 36,641 expressed sequence tags from laser capture microdissected adult mouse gastric and small intestinal epithelial progenitors, obtaining 4031 and 3324 unique transcripts, respectively. Using Gene Ontology ( GO) terms, each data set was compared with cDNA libraries from intact adult stomach and small intestine. Genes in GO categories enriched in progenitors were filtered against genes in GO categories represented in hematopoietic, neural, and embryonic stem cell transcriptomes and mapped onto transcription factor networks, plus canonical signal transduction and metabolic pathways. Wnt/beta-catenin, phosphoinositide-3/Akt kinase, insulin-like growth factor-1, vascular endothelial growth factor, integrin, and gamma-aminobutyric acid receptor signaling cascades, plus glycerolipid, fatty acid, and amino acid metabolic pathways are among those prominently represented in adult gut progenitors. The results reveal shared as well as distinctive features of adult gut stem cells when compared with other stem cell populations.
引用
收藏
页码:11292 / 11300
页数:9
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