Polymorphism of murine Fas ligand that affects the biological activity

dc.creatorKayagaki, Nobuhiko
dc.creatorYamaguchi, Noriko
dc.creatorNagao, Fumiko
dc.creatorMatsuo, Seishi
dc.creatorMaeda, Hiroaki
dc.creatorOkumura, Ko
dc.creatorYagita, Hideo
dc.date1997-04-15
dc.date.accessioned2026-08-02T20:16:27Z
dc.descriptionFas ligand (FasL) is a member of the tumor necrosis factor family and induces apoptosis in Fas (CD95)-bearing target cells. In this study, we generated several mAbs that react with mouse FasL (mFasL) and characterized their functional properties. One of these mAbs, K10, specifically reacted with mFasL derived from C57BL/6 (B6) mice, but not that from BALB/c mice as estimated by surface staining and blocking of cytotoxic activities of mFasL transfectants, suggesting a polymorphism of mFasL. Sequence analysis of mFasL cDNA from several strains revealed that BALB/c and DBA/2 mice have three nucleotide differences from the known B6 and C3H sequences, which result in two amino acid substitutions (Thr-184 → Ala-184 and Glu-218 → Gly-218) in the extracellular region. Analysis of the K10 reactivity and genotyping by PCR-restriction fragment length polymorphism revealed that inbred mice segregate into the following two allotypes: mFasL.1 (B6, C3H, MRL, SJL, NOD, NZB, NZW) and mFasL.2 (BALB/c, DBA/1, DBA/2). Interestingly, COS7 cells expressing BALB/c FasL lysed Fas-bearing target cells more efficiently than those expressing B6 FasL. Furthermore, BALB/c-derived CD8-FasL fusion protein, which is composed of the extracellular domains of human CD8α and mFasL, exhibited 9-fold higher specific activity than did B6-derived CD8-FasL. These results suggest that in mFasL.2 mice the Fas/FasL system works more effectively than in mFasL.1 mice.
dc.identifierhttps://pmc.ncbi.nlm.nih.gov/articles/PMC20542/
dc.identifierhttps://pubmed.ncbi.nlm.nih.gov/9108079/
dc.identifierhttps://doi.org/10.1073/pnas.94.8.3914
dc.identifier.urihttps://repo.dare.co.zw/handle/123456789/84813
dc.languageen
dc.publisherNational Academy of Sciences
dc.rightsCopyright © 1997, The National Academy of Sciences of the USA
dc.sourceProc Natl Acad Sci U S A
dc.subjectBiological Sciences
dc.titlePolymorphism of murine Fas ligand that affects the biological activity
dc.typeText

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