miR-146b correlates with increased disease activity and psoriatic tissue inflammation and promotes keratinocyte
Ling Zhang1, Shenglan Zhang2, Jianbin Wang1
1Department of Dermatology, Affiliated Hospital of Hebei University of Engineering, Handan, Hebei 056002, P.R. China.
Abstract:
The present study aimed to investigate the expression of microRNA (miR)-146b in psoriatic tissue and its correlation with psoriasis activity and inflammation. The effect of miR-146b overexpression on keratinocyte proliferation and apoptosis was also explored. The expression of miR-146b in the psoriasis-affected tissue and non-affected tissue of 110 patients was determined via reverse transcription-quantitative (RT-q)PCR. The psoriasis-affected body surface area and psoriasis area severity index (PASI) score were recorded for evaluating disease activity. The expression of various inflammatory cytokines in psoriasis-affected tissue was also detected via RT-qPCR. miR-146b overexpression and control plasmids were constructed and transfected into HaCaT cells in vitro. Subsequently, cell proliferation, apoptosis and tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL)-induced cell apoptosis were determined. The results revealed that the expression of miR-146b was increased in psoriasis-affected tissue compared with that in unaffected tissue. The results obtained from a receiver operating characteristic curve analysis demonstrated that miR-146b levels were able to discriminate between psoriasis-affected tissue and unaffected tissue, with an area under the curve value of 0.781 (95% CI: 0.720-0.843). In addition, miR-146b expression in psoriatic tissue was correlated with an increased PASI score in patients with psoriasis. miR-146b expression in psoriatic tissue was positively correlated with TNF-α, interleukin (IL)-6 and IL-17 mRNA levels. In vitro, miR-146b overexpression enhanced HaCaT cell proliferation and suppressed apoptosis as well as TRAIL-induced apoptosis when compared with that in control-transfected HaCaT cells. In conclusion, miR-146b was positively correlated with disease activity and psoriatic tissue inflammation. Keratinocyte proliferation was also promoted in psoriasis.
Insights
MicroRNA (miR)-146b is elevated in psoriasis, correlating with disease severity and inflammation. Overexpression of miR-146b promotes keratinocyte proliferation and inhibits apoptosis in psoriasis.
Area of Science:
- Dermatology
- Molecular Biology
- Immunology
Background:
- Psoriasis is a chronic inflammatory skin disease.
- MicroRNAs play crucial roles in regulating cellular processes and disease pathogenesis.
- The specific role of microRNA (miR)-146b in psoriasis remains to be fully elucidated.
Purpose of the Study:
- To investigate the expression levels of miR-146b in psoriatic skin tissue.
- To determine the correlation between miR-146b expression and psoriasis disease activity and inflammation.
- To explore the effects of miR-146b on keratinocyte proliferation and apoptosis in vitro.
Main Methods:
- Quantification of miR-146b expression in 110 patients' psoriatic and unaffected skin using reverse transcription-quantitative PCR (RT-qPCR).
- Assessment of disease activity using Psoriasis Area and Severity Index (PASI) scores and body surface area.
- In vitro study involving transfection of HaCaT cells with miR-146b overexpression plasmids to analyze cell proliferation and apoptosis.
Main Results:
- miR-146b expression was significantly increased in psoriatic tissue compared to unaffected tissue.
- miR-146b levels showed a positive correlation with PASI scores and inflammatory markers (TNF-α, IL-6, IL-17).
- Overexpression of miR-146b in HaCaT cells promoted proliferation and inhibited apoptosis, including TRAIL-induced apoptosis.
Conclusions:
- miR-146b is upregulated in psoriasis and is associated with disease activity and inflammation.
- miR-146b may contribute to the pathogenesis of psoriasis by promoting keratinocyte proliferation and inhibiting apoptosis.
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