INTERLEUKIN-1 BUT NOT TUMOR-NECROSIS-FACTOR-ALPHA SYNERGISTICALLY UP-REGULATES THE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR-INDUCEDB7-1 EXPRESSION OF MURINE LANGERHANS CELLS
M. Furue et al., INTERLEUKIN-1 BUT NOT TUMOR-NECROSIS-FACTOR-ALPHA SYNERGISTICALLY UP-REGULATES THE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR-INDUCEDB7-1 EXPRESSION OF MURINE LANGERHANS CELLS, British journal of dermatology, 135(2), 1996, pp. 194-198
Epidermal Langerhans cells (LC) express several co-stimulatory molecul
es such as B7/BB1, which has been implicated as one of the important d
eterminants for potent antigen-presenting function of LC. Recent studi
es have shown that B7/BB1 antigens comprise three distinct molecules t
ermed B7-1, B7-2 and B7-3. Previous studies have revealed that the phe
notypic and functional properties of murine LC are enormously affected
by various cytokines including granulocyte-macrophage colony stimulat
ing factor (GM-CSF), interleukin-1 (IL-1), and tumour necrosis factor
alpha (TNF-alpha) derived from surrounding keratinocytes. We have alre
ady demonstrated that the expression of B7-1 of murine LC is significa
ntly enhanced by GM-CSF, IL-1 or TNF-alpha. In this paper, we present
that IL-1, but not TNF-alpha, synergistically up-regulates the GM-CSF-
induced B7-1 expression of murine LC.