Transcriptome analysis identifies a robust gene expression program in the mouse intestinal epithelium on aging

被引:7
作者
Kazakevych, Juri [1 ]
Stoyanova, Elena [1 ]
Liebert, Anke [1 ,3 ]
Varga-Weisz, Patrick [1 ,2 ]
机构
[1] Babraham Inst, Cambridge CB22 3AT, England
[2] Univ Essex, Sch Biol Sci, Genom & Computat Biol, Colchester, Essex, England
[3] Francis Crick Inst, London NW1 1AT, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
INFLAMMATORY MONOCYTES; RECEPTORS; MICE; DIFFERENTIATION; PERMEABILITY; DYSFUNCTION; RECRUITMENT; IMMUNITY; MARKER; TISSUE;
D O I
10.1038/s41598-019-46966-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The intestinal epithelium undergoes constant regeneration driven by intestinal stem cells. How old age affects the transcriptome in this highly dynamic tissue is an important, but poorly explored question. Using transcriptomics on sorted intestinal stem cells and adult enterocytes, we identified candidate genes, which change expression on aging. Further validation of these on intestinal epithelium of multiple middle-aged versus old-aged mice highlighted the consistent up-regulation of the expression of the gene encoding chemokine receptor Ccr2, a mediator of inflammation and several disease processes. We observed also increased expression of Strc, coding for stereocilin, and dramatically decreased expression of Rps4l, coding for a ribosome subunit. Ccr2 and Rps4l are located close to the telomeric regions of chromosome 9 and 6, respectively. As only few genes were differentially expressed and we did not observe significant protein level changes of identified ageing markers, our analysis highlights the overall robustness of murine intestinal epithelium gene expression to old age.
引用
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页数:8
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