Nuclear localization of activated STAT6 and STAT3 in epidermis of prurigo nodularis

Br J Dermatol. 2011 Nov;165(5):990-6. doi: 10.1111/j.1365-2133.2011.10498.x. Epub 2011 Sep 29.

Abstract

Background: Prurigo nodularis (PN) is a chronic dermatitis characterized by discrete, raised, and firm papulonodules with intense pruritus. The pathogenesis still remains to be elucidated.

Objectives: To clarify the role of Th1 and Th2 cytokines in the pathogenesis of PN.

Methods: We examined the cytokine signatures, such as phosphorylation of STAT1, STAT3 and STAT6, HLA-DR and hyaluronan accumulation, to reveal the Th1 and Th2 cytokine influence on the lesional epidermis of PN.

Results: We first optimized antigen retrieval methods to detect these signatures with antibodies for phospho-STAT1 (pSTAT1), phospho-STAT3 (pSTAT3), phospho-STAT6 (pSTAT6), HLA-DR and hyaluronic acid binding protein (HABP) on the formalin-fixed paraffin-embedded sections of psoriasis, lichen planus and atopic dermatitis biopsy samples. Activation of STAT1 and STAT6 in epidermis by Th1 and Th2 cytokines was further confirmed in a cultured skin equivalent model treated with interferon-γ or interleukin (IL)-4/IL-13. With the relevant immunostaining methods, we examined the cytokine signatures in 22 cases of PN. The results revealed that (i) the entire epidermis of 19 cases was stained with anti-pSTAT6 antibody, (ii) 21 cases demonstrated nuclear staining with anti-pSTAT3 antibody, (iii) the entire epidermis of 21 cases was stained with HABP, (iv) the epidermis of eight cases showed scattered staining with anti-pSTAT1 antibody, and (v) six cases were positive for HLA-DR membrane expression.

Conclusions: These data indicated that Th2 cytokines related to STAT6 activation together with some unknown stimuli that activate STAT3 play a principal role in the pathogenesis of PN.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Nucleolus / chemistry*
  • Cytokines / physiology*
  • Epidermis / metabolism*
  • HLA-DR Antigens / metabolism
  • Humans
  • Hyaluronan Receptors / metabolism
  • Hyaluronic Acid / metabolism
  • Immunohistochemistry
  • Interferon-gamma / pharmacology
  • Interleukin-13 / pharmacology
  • Interleukin-4 / pharmacology
  • Phosphorylation
  • Prurigo / metabolism*
  • STAT1 Transcription Factor / metabolism
  • STAT3 Transcription Factor / metabolism*
  • STAT6 Transcription Factor / metabolism*
  • Th1 Cells / metabolism
  • Th2 Cells / metabolism

Substances

  • Cytokines
  • HLA-DR Antigens
  • Hyaluronan Receptors
  • Interleukin-13
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • STAT6 Transcription Factor
  • Interleukin-4
  • Interferon-gamma
  • Hyaluronic Acid