Copyright
©The Author(s) 2019.
World J Gastroenterol. Jan 21, 2019; 25(3): 330-345
Published online Jan 21, 2019. doi: 10.3748/wjg.v25.i3.330
Published online Jan 21, 2019. doi: 10.3748/wjg.v25.i3.330
Figure 5 NKX6.
3 depletion induces inflammatory cytokine expression in gastric epithelial cells. A: NKX6.3 depletion in HFE-145shNKX6.3 cells dramatically increased expression of inflammatory cytokines, including interleukin (IL)-1β, IL-6, and IL-8, and cyclooxygenase-2. Shown are the means ± SEM from three experiments. Superscript letter represents significant difference (aP < 0.005 and bP < 0.001). B and C: In HFE-145shNKX6.3 cells, silencing of apolipoprotein E (ApoE) with siApoE markedly inhibited oligomerization and aggregation of amyloid β and expression of nuclear factor kappa B p-p65 and inflammatory cytokines. Shown are the means ± SEM from three experiments. Superscript letter represents significant difference (cP < 0.05, dP < 0.005 and eP < 0.0001). IL: Interleukin; COX-2: Cyclooxygenase-2; ApoE: Apolipoprotein E; Aβ: Amyloid β; NF-κB: Nuclear factor kappa B.
- Citation: Yoon JH, Lee YS, Kim O, Ashktorab H, Smoot DT, Nam SW, Park WS. NKX6.3 protects against gastric mucosal atrophy by downregulating β-amyloid production. World J Gastroenterol 2019; 25(3): 330-345
- URL: https://www.wjgnet.com/1007-9327/full/v25/i3/330.htm
- DOI: https://dx.doi.org/10.3748/wjg.v25.i3.330