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Published on: February 27, 2019
hsa_circ_0087100/hsa-miR-6743-5p affects Th1 cell differentiation by regulating STAT1 in diabetic retinopathy
Shuai He1,2, Dongwei Lai1,2, Chenggong Ma3
1Department of Ophthalmology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, PR China.
Insights
The competitive endogenous RNA (ceRNA) network, specifically hsa_circ_0087100/hsa-miR-6743-5p/STAT1, influences Th1 cell differentiation in diabetic retinopathy (DR). This finding clarifies the role of ceRNA in DR immune infiltration.
Area of Science:
- Immunology
- Genetics
- Ophthalmology
Background:
- Diabetic retinopathy (DR) involves complex immune dysregulation.
- The role of competitive endogenous RNA (ceRNA) networks in DR-associated immune infiltration remains unclear.
Purpose of the Study:
- To investigate the function of the ceRNA network in immune cell infiltration within diabetic retinopathy.
- To identify specific ceRNA pathways contributing to Th1 cell differentiation in DR.
Main Methods:
- Utilized Gene Expression Omnibus data for differentially expressed circRNAs, miRNAs, and mRNAs.
- Employed CIBERSORT and ssGSEA for immune infiltration analysis.
- Conducted weighted gene co-expression network analysis to identify co-expressed genes.
- Validated STAT1-mediated Th1 differentiation in vitro and in vivo DR models.
Main Results:
- Identified the hsa_circ_0087100/hsa-miR-6743-5p/STAT1 axis as a key component in Th1 cell immune infiltration.
- Confirmed aberrant expression of this ceRNA network and STAT1-mediated Th1 differentiation in DR.
- Demonstrated the involvement of this pathway in both cellular and animal models of DR.
Conclusions:
- The hsa_circ_0087100/hsa-miR-6743-5p/STAT1 ceRNA network plays a significant role in modulating Th1 cell differentiation in diabetic retinopathy.
- This study provides novel insights into the molecular mechanisms underlying immune responses in DR.
Abstract:
Objective: To elucidate the role of the competitive endogenous RNA (ceRNA) network in immune infiltration of diabetic retinopathy (DR). Methods: We obtained differentially expressed (DE) circRNAs, miRNAs and mRNAs from the Gene Expression Omnibus database. Then, we identified immune infiltration by CIBERSORT and single-sample gene set enrichment analysis and discovered co-expression genes by weighted gene co-expression network analysis. Furthermore, STAT1-mediated Th1 differentiation was determined in DR cell models, DR patients and DR mouse models. Results: hsa_circ_0087100/hsa-miR-6743-5p/STAT1 was involved in immune infiltration of Th1 cells. Aberrant expression of the ceRNA network and STAT1-mediated Th1 differentiation was thus verified in vitro and in vivo. Conclusion: hsa_circ_0087100/hsa-miR-6743-5p/STAT1 may affect Th1 cell differentiation in DR.
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