Human peritoneal cells isolated from dialysis effluent have in vivo ma
turated human macrophages that could serve as a model for studying lip
oprotein metabolism and foam cell formation. We previously characteriz
ed the low density lipoprotein (LDL) and acetylated LDL (acetyl-LDL) r
eceptor activities of human total peritoneal cells. Now, we provide ev
idence that both LDL and acetyl-LDL stimulate acylCoA cholesterol:acyl
transferase (ACAT) activity of peritoneal cells. Prolonged incubation
of cells with LDL results in suppression of ACAT activity, while incu
bation with acetyl-LDL results in elevated and sustained enzyme activi
ty. When human peritoneal cells were analyzed using flow cytometry, th
e cell population showed reactivity for CD2, CD4, CD8, CD20, CD14 and
HLA-DR antigens. Purified human peritoneal mononuclear cells degraded
LDL. Human peritoneal macrophages formed foam cells when exposed to LD
L or acetyl-LDL in culture, and lipid deposition increased with incuba
tion time. Macrophages incubated in the presence of butylated hydroxy
toluene and LDL did not form foam cells.