Cyr61/CCN1 is involved in the pathogenesis of psoriasis vulgaris via promoting IL-8 production by keratinocytes in a JNK/NF-κB pathway

Clin Immunol. 2017 Jan:174:53-62. doi: 10.1016/j.clim.2016.11.003. Epub 2016 Nov 14.

Abstract

Purpose: Interleukin-8 (IL-8) is an important factor in the pathogenesis of psoriasis vulgaris, which is characterized by proliferation of keratinocytes, neutrophil infiltration and angiogenesis. Cysteine-rich 61 (Cyr61/CCN1), a secreted extracellular matrix protein, is a novel proinflammatory factor. Whether Cyr61 is involved in the development of psoriasis vulgaris via IL-8 production remains unknown. In this study we explore the role of Cyr61 in IL-8 expression regulation in vivo and in vitro.

Methods: Skin samples from normal donors and psoriasis vulgaris patients were examined the profile of Cyr61 and IL-8 using immunohistochemistry, real-time PCR and Western blotting. HaCaT cells were treated with Cyr61 and IL-8 expression was analyzed by real-time PCR and ELISA. Signal transduction pathways in Cyr61-induced IL-8 production were investigated by real-time PCR, western blotting, luciferase reporter assay or chromatin immunoprecipitation (ChIP) assay. IMQ-induced psoriasis-like mice were treated with anti-Cyr61monoclonal antibodies (mAb), or IgG1 as a control.

Results: We found that Cyr61 was abundant in the epidermis of patients with psoriasis vulgaris and positively correlated with the pathogenesis of skin lesions. Cyr61 induced IL-8 production by keratinocytes in a dose dependent manner. This IL-8 synthesis occurred in an IL-1β- and TNF-α- independent mode via PI3K, AKT and JNK activation, with binding of enhanced AP-1, C/EBPβ and NF-κB to sites located in the IL-8 promoter region. Treatment with anti-Cyr61 mAb led to reduction of MIP-2 level, decreased neutrophil infiltration, and attenuated inflammation in vivo.

Conclusions: Our results not only reveal a novel mechanism illustrating the role of Cyr61 in epidermis pathogenesis but also suggest that therapies targeting Cyr61 may represent a novel strategy in the treatment of psoriasis vulgaris.

Keywords: Cyr61; IL-8; Keratinocyte; Neutrophils; Pathogenesis; Psoriasis vulgaris.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Cell Line
  • Cysteine-Rich Protein 61 / genetics
  • Cysteine-Rich Protein 61 / immunology*
  • Female
  • Humans
  • Interleukin-1beta / genetics
  • Interleukin-8 / genetics
  • Interleukin-8 / immunology*
  • Keratinocytes / immunology
  • MAP Kinase Signaling System / immunology
  • Male
  • Mice, Inbred BALB C
  • Middle Aged
  • NF-kappa B / immunology
  • Psoriasis / immunology*
  • Psoriasis / pathology
  • RNA, Small Interfering / genetics
  • Skin / immunology
  • Skin / pathology
  • Tumor Necrosis Factor-alpha / genetics
  • Young Adult

Substances

  • Cysteine-Rich Protein 61
  • Interleukin-1beta
  • Interleukin-8
  • NF-kappa B
  • RNA, Small Interfering
  • Tumor Necrosis Factor-alpha