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• W2060956810 abstract "Suppressor cells were developed from nylon wool nonadherent CD4−8−TCRβ− bone marrow cells cocultured with parenchymal liver cells for 2.5 days. The major suppressor cell population consisted of nylon wool/plastic dish-adherent, phagocytic Mac-1+ CD3−4−8− cells (Ad cells), with 34% of the Ad cells being F4/80+. These Ad cells suppressed the antigen-specific proliferation of Th1 clones in an MHC-nonrestricted manner. They showed a dose-dependent increase in suppressive activity, with both NO and PGE2 levels in the culture supernatant rising with Ad cell concentration. OVA-pulsed Ad cells (OVA-Ad cells) were found to stimulate IFN-γ production, resulting in an elevation of the NO and PGE2 levels in wells containing OVA-specific Th1 clones. No DNA synthesis by these clones was detected in the absence of NG-monomethyl-l-arginine and indomethacin, yet the proliferation of the clone was induced in the presence of these chemicals. As proliferation is inhibited by NO and PGE2 the Ad cells give the impression that they have no antigen-presenting function. This function is MHC-class-II-restricted. If cells such as Ad cells did actually exist in the hepatic sinusoid, they could by their nature play a major role in inducing the early emerging unresponsiveness of T cells in the liver which we reported in a previous paper." @default.
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• W2060956810 date "1999-08-01" @default.
• W2060956810 modified "2023-10-18" @default.
• W2060956810 title "Cultured Murine Parenchymal Liver Cells Induce Differentiation of Bone Marrow Cells to Macrophage-like Cells Which Present Antigen to Th1 Clones but Inhibit Their Proliferation by Nitric Oxide and Prostaglandins" @default.
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• W2060956810 doi "https://doi.org/10.1006/cimm.1999.1540" @default.
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