Basic Study
Copyright ©The Author(s) 2018.
World J Gastroenterol. Mar 21, 2018; 24(11): 1196-1205
Published online Mar 21, 2018. doi: 10.3748/wjg.v24.i11.1196
Table 3 Genes selected for real-time PCR studies
TranscriptFold changes: patients vs controls
Details on function/ reasons to study
Basal+D, -L/P-D, +L/P+D, +L/P
MSR19.5613.1914.72macrophage scavenger receptor[49]; differentially expressed in 3 of 4 groups
CD1012.66expressed on various immune cells; inhibits expansion of colitogenic T cells[30]
CLEC5A2.823.11C-type lectin member 5A, pattern recognition receptor; involved in antibacterial/antiviral defense[43]
CLEC7A4.533.94C-type lectin member 7A, pattern recognition receptor; control of fungal infections[50]
CLEC12A6.044.52C-type lectin member 12A, pattern recognition receptor, inhibits cell death-induced inflammation[51]
ITGAM2.18CD11b; integrin αM; expressed by many immune cells; polymorphisms linked to autoimmunity[52]
LYZ3.512.03antimicrobial enzyme; essential role in innate immunity; increased production linked to CD[31]
PECAM13.15CD31; implicated in transendothelial leukocyte migration in experimental colitis[32]
CCL20-2.33-5.08chemokine expressed by neutrophils, enterocytes, Bcells and dendritic cell; IBD predilection gene[33]
CXCL5-38.89-5.32regulates neutrophil homeostasis and chemotaxis; increased serum levels in IBD patients reported[34]
IL-24-3.49-4.82Involved in host defence against bacteria and fungi; increased expression in patients with active IBD[35]
TREM1amplifier of antimicrobial immune responses and inflammation in experimental colitis and IBD[36]