TY - JOUR
T1 - Distinct microRNA expression profiles in follicle-associated epithelium and villous epithelium
AU - Nakato, Gaku
AU - Hase, Koji
AU - Ohno, Hiroshi
N1 - Funding Information:
This study was supported in part by Grant-in-Aid for Research Activity Start-up (G.N.) (Grant number: 22890238 ), Grants-in-Aid for Young Scientists (B) (G.N.) (Grant number: 24790485 ) and Young Scientists (A) (K.H.) (Grant number: 24249029 ), Scientific Research (A) (H.O.) (Grant number: 22689017 ) from the Japan Society for the Promotion of Science , Grant-in-Aid For Scientific Research on Priority Areas (K.H. and H.O.) (Grant number: 19041072 ) from the Ministry of Education, Culture, Sports, Science and Technology of Japan , Advanced Research and Development Programs for Medical Innovation from the Japan Agency for Medical Research and Development (H.O.) (Grant number: 15gm0710009h0002 ), and Sasakawa Scientific Research Grant from the Japan Science Society (G.N.) (Grant number: 22-453 ).
Publisher Copyright:
© 2015.
PY - 2015/9/1
Y1 - 2015/9/1
N2 - M cells in follicle-associated epithelium (FAE) covering intestinal lymphoid follicles serve as a portal of entry for particulate antigens (Kanaya and Ohno, 2014 [1]). Despite their biological significance, molecular mechanisms that govern M-cell differentiation and function have not been fully elucidated. MicroRNAs (miRNAs) have a role to control host gene expression profiles that modulate cellular physiology and characteristic. Many studies have shown that miRNAs regulate diverse biological processes including developmental timing, differentiation and growth control of cells and tissues (Ivey and Srivastava, 2010 [2]). miRNAs are also relevant to differentiation and function of intestinal epithelium (McKenna et al., 2010 [3]; Runtsch et al., 2014 [4]). Expression profiles and functions of miRNAs in the intestinal epithelium have been examined in jejunal and colonic mucosa [3]. In contrast, those in FAE remain uncharacterized. To address this deficiency, we isolated Peyer's Patch (PP) FAE and villous epithelium (VE) surrounding the FAE, and compared the miRNA expression profiles of FAE and VE by microarray analysis. This revealed that 43 miRNAs were up-regulated, whereas 9 miRNAs were down-regulated, in FAE compared to VE. A unique pattern of miRNA expression by FAE may reflect important diversity in cellular phenotypes and/or functional features of FAE. All microarray data has been deposited at GEO under accession number GSE46264.
AB - M cells in follicle-associated epithelium (FAE) covering intestinal lymphoid follicles serve as a portal of entry for particulate antigens (Kanaya and Ohno, 2014 [1]). Despite their biological significance, molecular mechanisms that govern M-cell differentiation and function have not been fully elucidated. MicroRNAs (miRNAs) have a role to control host gene expression profiles that modulate cellular physiology and characteristic. Many studies have shown that miRNAs regulate diverse biological processes including developmental timing, differentiation and growth control of cells and tissues (Ivey and Srivastava, 2010 [2]). miRNAs are also relevant to differentiation and function of intestinal epithelium (McKenna et al., 2010 [3]; Runtsch et al., 2014 [4]). Expression profiles and functions of miRNAs in the intestinal epithelium have been examined in jejunal and colonic mucosa [3]. In contrast, those in FAE remain uncharacterized. To address this deficiency, we isolated Peyer's Patch (PP) FAE and villous epithelium (VE) surrounding the FAE, and compared the miRNA expression profiles of FAE and VE by microarray analysis. This revealed that 43 miRNAs were up-regulated, whereas 9 miRNAs were down-regulated, in FAE compared to VE. A unique pattern of miRNA expression by FAE may reflect important diversity in cellular phenotypes and/or functional features of FAE. All microarray data has been deposited at GEO under accession number GSE46264.
KW - Follicle-associated epithelium
KW - M cell
KW - MicroRNA
KW - Peyer's patch
KW - Villus epithelium
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U2 - 10.1016/j.gdata.2015.07.011
DO - 10.1016/j.gdata.2015.07.011
M3 - Article
AN - SCOPUS:84938057677
SN - 2213-5960
VL - 5
SP - 388
EP - 390
JO - Genomics Data
JF - Genomics Data
ER -