Ca. Feghali et al., CONTROL OF IL-6 EXPRESSION AND RESPONSE IN FIBROBLASTS FROM PATIENTS WITH SYSTEMIC-SCLEROSIS, Autoimmunity, 17(4), 1994, pp. 309-318
Systemic sclerosis (SSc) is an autoimmune connective tissue disease of
unknown etiology in which aberrant fibroblast Function results in fib
rosis of the skin and internal organs. A distinguishing feature of der
mal fibroblasts cultured from SSc lesions is that they produce constit
utively, i.e., without exogenous stimulation, as much as 30-fold more
interleukin-6 (IL-6) than do normal fibroblasts. The present study ind
icates that the mechanism of constitutive IL-6 secretion involves the
accumulation of IL-6 mRNA in affected SSc fibroblasts, mediated by the
constitutive binding of nuclear factors to the IL-6 promoter. DNA-pro
tein complexes formed using nuclear extracts of constitutively express
ing cells are distinct from those using extracts of normal cells, with
or without exogenous stimulation of IL-6; thus, the mechanisms which
regulate constitutive and inducible IL-6 gene expression are apparentl
y distinct. The data also demonstrate that dermal fibroblasts respond
very rapidly to IL-6 by increasing expression of the IL-6 gene, thus s
uggesting a mechanism for the establishment and/or persistence of cons
titutive expression. The constitutive secretion of IL-6 may play an im
portant role in the perpetuation of the local immune dysregulation and
fibroblast activation in the SSc lesion.