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Updated: Jul 19, 2025

Induction of Murine Intestinal Inflammation by Adoptive Transfer of Effector CD4+CD45RBhigh T Cells into Immunodeficient Mice
Published on: April 21, 2015
Ovotransferrin Inhibits TNF-α Induced Inflammatory Response in Gastric Epithelial Cells via MAPK and NF-κB Pathway
Yan Huang1,2,3, Shuping Chen1,2,3, Yao Yao1,2,3
1Jiangxi Key Laboratory of Natural Products and Functional Food, Jiangxi Agricultural University, Nanchang 330045, China.
Abstract:
Ovotransferrin (OVT) has been confirmed to have anti-inflammatory activity. However, its effect and mechanism on gastric inflammation are unclear. In this study, the effect and mechanism of the OVT on the tumor necrosis factor-α (TNF-α) induced inflammatory response in gastric epithelial cells (GES-1) were investigated. The enzyme linked immunosorbent assay (ELISA) was used to determine the levels of inflammation cytokines, followed by RNA sequencing to explore the potential pathways of its anti-inflammatory effect, and then it was validated by Western blotting and pathways inhibitors. Results showed that the OVT at concentrations of 50-400 μg/mL displayed nontoxicity against GES-1 cells. Additionally, 100 μg/mL of OVT obviously reduced the secretion of interleukin (IL)-8, IL-6, and TNF-α by 63.02% (630.09/1703.98), 35.53% (935.81/1451.43), and 36.19% (964.60/1511.63), respectively. The results of RNA sequencing exhibited that the OVT significantly influences the activation of mitogen-activated protein kinase (MAPK) and the nuclear factor kappa-light-chain enhancer of activated B cell (NF-κB) pathways, which was verified by the levels of p-IKK, p-IκB, p-P65, p-ERK, p-JNK, and p-P38 protein. IL-8 contents released by GES-1 cells after incubation with inhibitors of NF-κB and MAPK pathways further confirmed that OVT hindered activation of these two pathways. Collectively, these results suggested that OVT was a natural protein with the potential to treat gastric inflammation.
Insights
Ovotransferrin (OVT) effectively reduces gastric inflammation by inhibiting key inflammatory cytokines like IL-8, IL-6, and TNF-α. This natural protein works by suppressing the MAPK and NF-κB signaling pathways, showing potential for treating gastric inflammation.
Area of Science:
- Gastroenterology and Immunology
- Biochemistry and Molecular Biology
Background:
- Ovotransferrin (OVT) possesses known anti-inflammatory properties.
- The specific mechanisms of OVT's action on gastric inflammation remain largely uncharacterized.
Purpose of the Study:
- To investigate the anti-inflammatory effects of Ovotransferrin (OVT) on gastric epithelial cells (GES-1) stimulated with tumor necrosis factor-α (TNF-α).
- To elucidate the underlying molecular mechanisms, particularly the involvement of MAPK and NF-κB signaling pathways.
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) for quantifying inflammatory cytokines.
- RNA sequencing to identify affected cellular pathways.
- Western blotting and pathway inhibitors to validate molecular mechanisms.
Main Results:
- Ovotransferrin (OVT) demonstrated no toxicity to GES-1 cells at tested concentrations (50-400 μg/mL).
- OVT significantly reduced the secretion of interleukin-8 (IL-8), IL-6, and TNF-α.
- RNA sequencing and subsequent validation confirmed OVT's inhibition of mitogen-activated protein kinase (MAPK) and nuclear factor kappa-light-chain enhancer of activated B cell (NF-κB) pathways.
Conclusions:
- Ovotransferrin (OVT) exhibits significant anti-inflammatory effects in gastric epithelial cells.
- OVT exerts its protective effects by modulating the MAPK and NF-κB signaling cascades.
- OVT is a promising natural protein therapeutic candidate for managing gastric inflammation.
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