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Alleviation of imiquimod-induced psoriasis-like symptoms in Rorα-deficient mouse skin
Koog Chan Park1, Jiwon Kim2, Aram Lee1
1Research Institute of Women's Health, Sookmyung Women's University, Seoul 04310; Department of Biological Sciences, Cellular Heterogeneity Research Center, Sookmyung Women's University, Seoul 04310, Korea.
Abstract:
Retinoic acid receptor-related orphan receptor α (RORα) plays a vital role in various physiological processes, including metabolism, cancer, circadian rhythm, cerebellar development, and inflammation. Although RORα is expressed in the skin, its role in skin physiology remains poorly elucidated. Herein, Rorα was expressed in the basal and suprabasal layers of the epidermis; however, keratinocyte-specific Rorα deletion did not impact normal epidermal formation. Under pathophysiological conditions, Rorα-deficient mice exhibited alleviated psoriasis-like symptoms, including relatively intact epidermal stratification, reduced keratinocyte hyperproliferation, and low-level expression of inflammatory cytokines in keratinocytes. Unexpectedly, the splenic population of Th17 cells was significantly lower in keratinocytespecific RORα deficient mice than in the control. Additionally, Rorα-deficiency reduced imiquimod-induced activation of nuclear factor-κB and STAT3 in keratinocytes. Therefore, we expect that RORα inhibitors act on immune cells and keratinocytes to suppress the onset and progression of psoriasis.as an adjuvant for cancer immunotherapy. [BMB Reports 2023; 56(5): 296-301].
Insights
Retinoic acid receptor-related orphan receptor α (RORα) deficiency alleviates psoriasis-like symptoms by reducing inflammation and keratinocyte hyperproliferation. RORα inhibition may offer a therapeutic strategy for treating psoriasis.
Area of Science:
- Dermatology
- Immunology
- Molecular Biology
Background:
- Retinoic acid receptor-related orphan receptor α (RORα) is involved in various physiological processes but its role in skin remains unclear.
- RORα is expressed in epidermal layers, but its absence does not affect normal epidermal development.
Discussion:
- RORα deficiency ameliorates psoriasis-like symptoms in mice, characterized by improved epidermal stratification and reduced keratinocyte proliferation.
- A significant decrease in splenic Th17 cells was observed in RORα-deficient mice.
- RORα deficiency suppresses imiquimod-induced activation of NF-κB and STAT3 pathways in keratinocytes.
Key Insights:
- RORα plays a role in keratinocyte inflammatory responses and Th17 cell populations.
- Targeting RORα could be a novel therapeutic approach for psoriasis.
- RORα inhibitors may impact both immune cells and keratinocytes in psoriasis pathogenesis.
Outlook:
- RORα inhibitors show potential for treating psoriasis by modulating immune responses and keratinocyte activity.
- Further research is needed to explore RORα's precise mechanisms in skin inflammation.
- RORα inhibition could be investigated as an adjuvant therapy in cancer immunotherapy.
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