Resolvin D1 protects against Aspergillus fumigatus keratitis in diabetes by blocking the MAPK-NF-κB pathway
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Updated: Oct 5, 2025

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Published on: June 9, 2021
1Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, Jiangsu, 210008, China; Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, Nanjing, Jiangsu, 210008, China; Nanjing Drum Tower Hospital Clinical College of Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210008, China.
Abstract:
Fungal keratitis (FK) is one of the main causes of blindness in China. People with diabetes are susceptible to corneal epithelial disease, even fungal keratitis. At present, there are few studies on this disease. Resolvins (Rv) has been reported as a mediators that exert crucial anti-inflammatory and immune regulation roles in serval diseases. In order to investigate the roles and underlying mechanism of Resolvins D1 (RvD1) on the Aspergillus fumigatus (A. fumigatus) keratitis in diabetes, we established in vivo and in vitro models of A. fumigatus keratitis, which were then exposed to high glucose. The expression levels of RvD1, 5-lipoxygenase (5-LOX), and 15-lipoxygenase (15-LOX) in A. fumigatus keratitis patients with diabetes were determined through Enzyme Linked Immunosorbent Assay (ELISA), Western blot and immunohistochemistry. Reactive Oxygen Species (ROS) production, ELISA, flow cytometry, Hematoxylin-Eosin (HE) staining and fungal loading determination were conducted to evaluate the severity of A. fumigatus infection. Lymphangiogenesis and angiogenesis were examined by immunofluorescence assay. Western blot was applied to detect the proteins of the MAPK-NF-κB pathway. The results showed that RvD1 diminished the high glucose-induced oxidative stress and inflammatory response, as evidenced by the reduction of ROS production, Interleukin-6 (IL-6), Interleukin-8 (IL-8), Heme Oxygenase-1 (HMOX-1), and the elevation of Cyclooxygenase-2 (COX2), Superoxide Dismutase (SOD-1), and Glutathione Peroxidase-2 (GPX2) levels in A. fumigatus-infected Human Corneal Endothelial Cells (HCECs). Additionally, lymphangiogenesis and angiogenesis prominently decreased after intervention with RvD1. Furthermore, RvD1 significantly reduced the levels of p-MEK1/2 and p-ERK1/2, and restrained the NF-κB and GPR32 activation. The above results showed that RvD1 protects against A. fumigatus keratitis in diabetes by suppressing oxidative stress, inflammatory response, fungal growth, and immunoreaction via modulating MAPK-NF-κB pathway. RvD1 provides clues for the therapeutic targets of Fungal keratitis complicated with diabetes.
Insights
Resolvin D1 (RvD1) effectively treats fungal keratitis in diabetic patients by reducing inflammation and oxidative stress. This study highlights RvD1 as a potential therapeutic target for fungal keratitis complicated with diabetes.
Area of Science:
- Ophthalmology
- Immunology
- Endocrinology
Background:
- Fungal keratitis (FK) is a significant cause of blindness, particularly in China.
- Diabetic patients are at increased risk for corneal epithelial diseases, including FK.
- Limited research exists on FK in diabetic individuals and the role of resolvins.
Purpose of the Study:
- To investigate the therapeutic effects and underlying mechanisms of Resolvin D1 (RvD1) in Aspergillus fumigatus (A. fumigatus) keratitis in a diabetic model.
- To explore RvD1's impact on oxidative stress, inflammation, and related signaling pathways in A. fumigatus keratitis.
Main Methods:
- Established in vivo and in vitro models of A. fumigatus keratitis under high glucose conditions.
- Measured RvD1, 5-lipoxygenase (5-LOX), and 15-lipoxygenase (15-LOX) levels via ELISA, Western blot, and immunohistochemistry.
- Assessed oxidative stress (ROS), inflammation (cytokines), fungal load, and angiogenesis/lymphangiogenesis; analyzed MAPK-NF-κB pathway activation.
Main Results:
- RvD1 reduced high glucose-induced oxidative stress and inflammation in infected Human Corneal Endothelial Cells (HCECs).
- RvD1 decreased ROS, IL-6, IL-8, and HMOX-1, while increasing COX2, SOD-1, and GPX2.
- RvD1 inhibited lymphangiogenesis, angiogenesis, and suppressed the MAPK-NF-κB pathway (p-MEK1/2, p-ERK1/2, NF-κB, GPR32 activation).
Conclusions:
- RvD1 demonstrates protective effects against A. fumigatus keratitis in diabetes.
- RvD1 acts by suppressing oxidative stress, inflammation, fungal growth, and immunoreaction through the MAPK-NF-κB pathway.
- RvD1 presents a promising therapeutic target for fungal keratitis in diabetic patients.
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