Increased skin barrier disruption by sodium lauryl sulfate in mice expressing a constitutively active STAT6 in T cells

Research output: Contribution to journalArticle

18 Scopus citations


Atopic dermatitis (AD) is a pruritic, chronic inflammatory skin disease that affects 10-20% of children and 1-3% of adults worldwide. Recent studies have indicated that the ability of Th2 cytokines, such as interleukin-4 (IL-4) to regulate skin barrier function may be a predisposing factor for AD development. The present studies examined the ability of increased Th2 activity to affect cutaneous barrier function in vivo and epidermal thickening. Mice that express a constitutively active Signal Transducer and Activator of Transcription 6 (STAT6VT) have increased Th2 cells and a predisposition to allergic inflammation were used in these studies, they demonstrate that topical treatment with the irritant sodium lauryl sulfate (SLS) caused increased transepidermal water loss and epidermal thickening in STAT6VT mice over similarly treated wild-type mice. The proliferation marker Ki-67 was increased in the epidermis of STAT6VT compared to the wild-type mice. However, these differences do not appear to be linked to the addition of an irritant as control-treated STAT6VT skin also exhibited elevated Ki-67 levels, suggesting that the increased epidermal thickness in SLS-treated STAT6VT mice is primarily driven by epidermal cell hypertrophy rather than an increase in cellular proliferation. Our results suggest that an environment with increased Th2 cytokines results in abnormal responses to topical irritants.

Original languageEnglish (US)
Pages (from-to)65-71
Number of pages7
JournalArchives of Dermatological Research
Issue number1
StatePublished - Jan 2012


  • Atopic dermatitis
  • Interleukin-4
  • STAT6 V547A/T548A mutation
  • T-helper type 2 cells
  • Transepidermal water loss

ASJC Scopus subject areas

  • Dermatology

Fingerprint Dive into the research topics of 'Increased skin barrier disruption by sodium lauryl sulfate in mice expressing a constitutively active STAT6 in T cells'. Together they form a unique fingerprint.

  • Cite this