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Negative Regulation of Semaphorin-3A Expression in Peripheral Blood Mononuclear Cells Using MicroRNA-497-5p
Shima Shapoori1, Mazdak Ganjalikhani-Hakemi1, Mahsa Rezaeepoor1
1Department of Immunology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Background:
Semaphorin-3A (Sema3A), as a secreted semaphorin, is an immune modulator molecule participating in the pathogenesis of autoimmune diseases. MicroRNAs (miRNAs) modulate the target-gene expression at the post-transcriptional level. It has been proposed that miRNAs may be crucial to the modulation of the function of semaphorins. Previous findings have proven that miR-497-5p is upregulated and Sema3A is downregulated in some autoimmune disorders. Thus, we aimed to examine the presence of any correlation between Sema3A and miR-497-5p in peripheral blood mononuclear cells (PBMCs).
Methods:
PBMCs were cultured and transfected with miR-497-5p mimic using the X-tremeGENE™ reagent. The expression level of Sema3A was assessed after 48 hours in supernatants and cells via the enzyme-linked immunosorbent assay and quantitative real-time polymerase chain reaction, respectively. Cell viability was evaluated using the methylthiazol tetrazolium assay. All the experiments were done in triplicate, and the statistical analyses were performed with SPSS, version 20. P values equal to or less than 0.05 were considered significant.
Results:
We observed downregulation of the Sema3A gene (P=0.0001) and its secretion (P=0.032) in the PBMCs through miR-497-5p transfection. Moreover, transfection with miR-497-5p mimic and downregulation of Sema3A did not affect the viability of the PBMCs (P=0.061).
Conclusion:
Based on the obtained results, we suggest that miR-497-5p has a high suppressive effect on Sema3A expression and both Sema3A and miR-497-5p can be considered critical targets for further studies on future therapeutic attempts for the treatment of autoimmune diseases such as multiple sclerosis and rheumatoid arthritis.
Insights
MicroRNA-497-5p suppresses Semaphorin-3A expression in immune cells, suggesting potential therapeutic targets for autoimmune diseases like multiple sclerosis and rheumatoid arthritis.
Area of Science:
- Immunology
- Molecular Biology
- Genetics
Background:
- Semaphorin-3A (Sema3A) is an immune modulator implicated in autoimmune disease pathogenesis.
- MicroRNAs (miRNAs) regulate gene expression post-transcriptionally and may influence semaphorin function.
- Previous studies indicate elevated miR-497-5p and reduced Sema3A in certain autoimmune disorders.
Purpose of the Study:
- To investigate the correlation between Sema3A and miR-497-5p in peripheral blood mononuclear cells (PBMCs).
- To determine the effect of miR-497-5p on Sema3A expression in PBMCs.
Main Methods:
- PBMCs were transfected with a miR-497-5p mimic.
- Sema3A expression and secretion were measured using ELISA and qPCR.
- Cell viability was assessed via MTT assay.
Main Results:
- Transfection with miR-497-5p mimic significantly downregulated Sema3A gene expression (P=0.0001) and secretion (P=0.032).
- miR-497-5p mimic transfection and subsequent Sema3A downregulation did not impact PBMC viability (P=0.061).
Conclusions:
- miR-497-5p exhibits a potent suppressive effect on Sema3A expression.
- Both Sema3A and miR-497-5p represent promising therapeutic targets for autoimmune diseases, including multiple sclerosis and rheumatoid arthritis.
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