The expression of Fas-ligand (Fas-L) on microglia could be relevant in multiple sclerosis immunopathology. The present study was performed to evaluate in vitro the expression of Fas-L in human microglial cells both unstimulated and after stimulation with IFN-gamma, beta-IFN-1b and beta-IFN-1b+IFN-gamma. Cells were stimulated for 6,12,24 and 48 h. Surface Fas-L was evaluated by flow cytometry, total Fas-L by Western blot, whereas mRNA for Fas-L was measured by RT-PCR. We also evaluated the capacity of microglial cells to induce, in vitro, apoptosis on Fas-positive T leukemia Jurkat cells. Our results showed a constitutive expression of Fas-L on microglia. IFN-gamma downregulated the expression of the molecule, while beta-IFN-1b and beta-IFN-1b+IFN-gamma did not. The amount of surface Fas-L was related to the ability of microglial cells to induce apoptosis in Fas-positive target cells, which was partly inhibited by blockade of the Fas-Fas-L pathway. (C) 2000 published by Elsevier Science B.V. All rights reserved.
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USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
Mincheff, M
;
Loukinov, D
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USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
Loukinov, D
;
Zoubak, S
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USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
Zoubak, S
;
Hammett, M
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USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
Hammett, M
;
Meryman, H
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USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
机构:
Univ Queensland, Royal Brisbane Hosp, Dept Med, Neuroimmunol Res Unit, Brisbane, Qld 4029, AustraliaUniv Queensland, Royal Brisbane Hosp, Dept Med, Neuroimmunol Res Unit, Brisbane, Qld 4029, Australia
White, CA
;
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McCombe, PA
;
Pender, MP
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Univ Queensland, Royal Brisbane Hosp, Dept Med, Neuroimmunol Res Unit, Brisbane, Qld 4029, AustraliaUniv Queensland, Royal Brisbane Hosp, Dept Med, Neuroimmunol Res Unit, Brisbane, Qld 4029, Australia
机构:
USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
Mincheff, M
;
Loukinov, D
论文数: 0引用数: 0
h-index: 0
机构:
USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
Loukinov, D
;
Zoubak, S
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机构:
USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
Zoubak, S
;
Hammett, M
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机构:
USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
Hammett, M
;
Meryman, H
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USN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USAUSN, Transfus & Cryopreservat Res Program, Med Res Inst, Med Ctr, Bethesda, MD 20889 USA
机构:
Univ Queensland, Royal Brisbane Hosp, Dept Med, Neuroimmunol Res Unit, Brisbane, Qld 4029, AustraliaUniv Queensland, Royal Brisbane Hosp, Dept Med, Neuroimmunol Res Unit, Brisbane, Qld 4029, Australia
White, CA
;
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h-index:
机构:
McCombe, PA
;
Pender, MP
论文数: 0引用数: 0
h-index: 0
机构:
Univ Queensland, Royal Brisbane Hosp, Dept Med, Neuroimmunol Res Unit, Brisbane, Qld 4029, AustraliaUniv Queensland, Royal Brisbane Hosp, Dept Med, Neuroimmunol Res Unit, Brisbane, Qld 4029, Australia