Defect of IL17 Signaling, but Not Centrinone, Inhibits the Development of Psoriasis and Skin Papilloma in Mouse Models

Ben Jin; Yongfeng Zhang; Haiyan D Miller; Ling He; Dongxia Ge; Alun R Wang; Zongbing You

doi:10.3390/biomedicines10081976

Defect of IL17 Signaling, but Not Centrinone, Inhibits the Development of Psoriasis and Skin Papilloma in Mouse Models

Biomedicines. 2022 Aug 15;10(8):1976. doi: 10.3390/biomedicines10081976.

Authors

Ben Jin^{1

2}, Yongfeng Zhang², Haiyan D Miller^{1

2}, Ling He², Dongxia Ge^{2

3}, Alun R Wang⁴, Zongbing You^{1

2

3

5

6

7}

Affiliations

¹ Southeast Louisiana Veterans Health Care System, New Orleans, LA 70119, USA.
² Department of Structural & Cellular Biology, Tulane University, New Orleans, LA 70112, USA.
³ Department of Orthopaedic Surgery, Tulane University, New Orleans, LA 70112, USA.
⁴ Department of Pathology and Laboratory Medicine, Tulane University, New Orleans, LA 70112, USA.
⁵ Tulane Cancer Center and Louisiana Cancer Research Consortium, Tulane University, New Orleans, LA 70112, USA.
⁶ Tulane Center for Stem Cell Research and Regenerative Medicine, Tulane University, New Orleans, LA 70112, USA.
⁷ Tulane Center for Aging, Tulane University, New Orleans, LA 70112, USA.

Abstract

Patients with psoriasis tend to develop skin cancer, and the hyperproliferation of the epidermis is a histopathological hallmark of both psoriasis and cutaneous squamous cell carcinoma (SCC), indicating that they may share pathogenic mechanisms. Interleukin-17 (IL17) stimulates the proliferation of the epidermis, leading to psoriasis. Overexpression of Polo-like kinase 4 (PLK4), which controls centriole duplication, has been identified in SCC, which also shows the hyperproliferation of keratinocytes. To investigate the cooperation between IL17 signaling and centriole duplication in epidermal proliferation, we established psoriasis and skin papilloma models in wild type (WT), IL17 receptor A (T779A) knockin (Il17ra(T779A)-KI), and IL17 receptor C knockout (Il17rc-KO) mouse strains. Bioinformatics, Western blot, immunohistochemical staining, colony formation, and real-time PCR were used to determine the effect of IL17 signaling and centrinone on epithelial proliferation. In the psoriasis model, compared to WT and Il17ra(T779A)-KI, Il17rc-KO dramatically suppressed epidermal thickening. The proliferation of keratinocytes significantly decreased in this order from WT to Il17ra(T779A)-KI and Il17rc-KO mice. In the skin papilloma model, Il17ra(T779A)-KI significantly decreased tumor burden compared to the WT, while Il17rc-KO abolished papilloma development. However, centrinone, a selective inhibitor of PLK4, did not affect skin lesion formation in either model. Our data demonstrated that Il17ra(T779A)-KI and Il17rc-KO prevent the development of psoriasis and tumorigenesis in the skin, while the topical administration of centrinone does not have any effect.

Keywords: IL17RA; IL17RC; centrinone; psoriasis; skin papilloma.

Abstract

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