Activated B cells express functional Fas ligand.


Autoria(s): Hahne M.; Renno T.; Schroeter M.; Irmler M.; French L.; Bornard T.; MacDonald H.R.; Tschopp J.
Data(s)

1996

Resumo

Fas ligand (FasL, Apo-1L) is a member of the tumor necrosis factor protein family and binding to its receptor (Fas, Apo-1, CD95) triggers cell death through apoptosis. Ligand expression is restricted to cells with known cytolytic activity and found on hematopoietic cells of the T cell and natural killer lineage. Here we provide evidence that B lymphocytes can express FasL. Flow cytometric analysis revealed that FasL is expressed on the surface of B cells upon stimulation with either lipopolysaccharide or phorbol 12-myristate 13-acetate/ionomycin. FasL expression on activated B cells was confirmed by western blot and reverse transcriptase polymerase chain reaction analysis. FasL on B cells is functional since lipopolysaccharide-activated B lymphocytes derived from wild type, but not from gld mutant mice, were able to kill Fas-sensitive target cells. Our data suggest that the Fas system may contribute to the control of B cell homeostasis.

Identificador

http://serval.unil.ch/?id=serval:BIB_A6BC9CA56CF8

isbn:0014-2980

pmid:8605944

doi:10.1002/eji.1830260332

isiid:A1996UJ76800031

Idioma(s)

en

Fonte

European journal of immunology, vol. 26, no. 3, pp. 721-724

Palavras-Chave #Amino Acid Sequence; Animals; Antigens, CD95/biosynthesis; Antigens, CD95/physiology; B-Lymphocytes/drug effects; B-Lymphocytes/immunology; Base Sequence; Cytotoxicity, Immunologic/drug effects; Fas Ligand Protein; Ligands; Lipopolysaccharides/pharmacology; Lymphocyte Activation; Membrane Glycoproteins/biosynthesis; Membrane Glycoproteins/physiology; Mice; Mice, Inbred BALB C; Molecular Sequence Data; Tumor Necrosis Factor-alpha/physiology
Tipo

info:eu-repo/semantics/article

article