Observational Study
Copyright ©The Author(s) 2019.
World J Gastroenterol. Nov 21, 2019; 25(43): 6465-6482
Published online Nov 21, 2019. doi: 10.3748/wjg.v25.i43.6465
Figure 5
Figure 5 Functional phenotype of immune cells in colonic mucosa. A: The graph and representative FACS plots displaying the percentage of CD8+ T cells derived from colonic mucosa of ulcerative colitis (UC) patients without and with metabolic syndrome (MetS). B: The graph and representative FACS plots displaying the percentage of T regulatory cells (CD4+Fox3+) derived from colonic mucosa of UC patients without and with MetS. C: The graph and representative FACS plots displaying the percentage of Galectin-3+ (Gal-3+) NKT (CD3+CD56+) cells derived from colonic mucosa of UC patients without and with MetS. D: The graph and representative FACS plots displaying the percentage of CD8+Foxp3+ cells derived from colonic mucosa of UC patients without and with MetS. E and F: The graph and representative FACS plots displaying the percentage of Interleukin-10 producing CD56+ and CD4+ cells derived from colonic mucosa of UC patients without and with MetS. Cellular make up of colon-infiltrating immune cells were examined by flow cytometry. The Student’s t or Mann-Whitney U test was applied to evaluate statistical significant differences among the two groups. IL-10: Interleukin-10; Gal-3: Galectin-3.