The current work examines the expression of acute phase genes in a mur
ine-derived bone marrow stromal cell model (BMS2) which exhibits adipo
cyte and osteoblast characteristics and supports lymphopoiesis in vitr
o. Each of these physiologic processes is responsive to inflammatory e
vents such as endotoxemia. Exposure of BMS2 cells to pro-inflammatory
cytokines induced the expression of the serum amyloid A and complement
factor B. During adipocyte differentiation, expression of complement
C3, complement factor D (adipsin), and angiotensinogen increased in a
time dependent manner. The bone metabolic steroid, 1,25 dihydroxy vita
min D-3, specifically induced complement C3 expression in a time- and
dose-dependent manner. Based on get retention analysis, BMS2 nuclear e
xtract contained proteins recognizing specific response elements from
the complement C3, angiotensinogen, and complement factor B promoters.
These results suggest that the bone marrow's repertoire of acute phas
e proteins is dependent on the stromal cell's phenotype or activation
state.