PPAR delta is a type 1 IFN target gene and inhibits apoptosis in T cells

Nadya al Yacoub, Malgorzata Romanowska, Sybille Krauss, Susann Schweiger, John Foerster

    Research output: Contribution to journalArticle

    23 Citations (Scopus)

    Abstract

    Peroxisome proliferator-activated receptor beta/delta (PPAR delta) is a nuclear hormone receptor regulating diverse biological processes, including beta-oxidation of fatty acid and epithelial cell differentiation. To date, the role of PPAR delta in the immune system has not been thoroughly studied. Here, we show that PPAR delta is expressed in activated human T cells purified from peripheral blood as well as in T cells isolated from affected psoriasis skin lesions. PPAR delta is induced in T cells on stimulation with type 1 IFN. Functionally, PPAR delta enhances proliferation of primary T cells and blocks apoptosis induced by type 1 IFN and by serum deprivation. We show that these cellular functions are mediated by the activation of extracellular signal-regulated kinase1/2 signaling. Our results (1) establish a direct molecular link between type 1 IFN signaling and PPAR delta, (2) define a functional role for PPAR delta in human T cells, and (3) suggest that the induction of PPAR delta by type 1 IFN contributes to the persistence of activated T cells in psoriasis skin lesions.

    Original languageEnglish
    Pages (from-to)1940-1949
    Number of pages10
    JournalJournal of Investigative Dermatology
    Volume128
    Issue number8
    DOIs
    Publication statusPublished - Aug 2008

    Keywords

    • PROLIFERATOR-ACTIVATED-RECEPTOR
    • LESIONAL PSORIATIC SKIN
    • GROWTH-FACTOR
    • NUCLEAR RECEPTOR
    • GAMMA AGONISTS
    • INDUCE APOPTOSIS
    • DENDRITIC CELLS
    • LYMPHOCYTES
    • EXPRESSION
    • BINDING

    Cite this

    al Yacoub, Nadya ; Romanowska, Malgorzata ; Krauss, Sybille ; Schweiger, Susann ; Foerster, John. / PPAR delta is a type 1 IFN target gene and inhibits apoptosis in T cells. In: Journal of Investigative Dermatology. 2008 ; Vol. 128, No. 8. pp. 1940-1949.
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    abstract = "Peroxisome proliferator-activated receptor beta/delta (PPAR delta) is a nuclear hormone receptor regulating diverse biological processes, including beta-oxidation of fatty acid and epithelial cell differentiation. To date, the role of PPAR delta in the immune system has not been thoroughly studied. Here, we show that PPAR delta is expressed in activated human T cells purified from peripheral blood as well as in T cells isolated from affected psoriasis skin lesions. PPAR delta is induced in T cells on stimulation with type 1 IFN. Functionally, PPAR delta enhances proliferation of primary T cells and blocks apoptosis induced by type 1 IFN and by serum deprivation. We show that these cellular functions are mediated by the activation of extracellular signal-regulated kinase1/2 signaling. Our results (1) establish a direct molecular link between type 1 IFN signaling and PPAR delta, (2) define a functional role for PPAR delta in human T cells, and (3) suggest that the induction of PPAR delta by type 1 IFN contributes to the persistence of activated T cells in psoriasis skin lesions.",
    keywords = "PROLIFERATOR-ACTIVATED-RECEPTOR, LESIONAL PSORIATIC SKIN, GROWTH-FACTOR, NUCLEAR RECEPTOR, GAMMA AGONISTS, INDUCE APOPTOSIS, DENDRITIC CELLS, LYMPHOCYTES, EXPRESSION, BINDING",
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    PPAR delta is a type 1 IFN target gene and inhibits apoptosis in T cells. / al Yacoub, Nadya; Romanowska, Malgorzata; Krauss, Sybille; Schweiger, Susann; Foerster, John.

    In: Journal of Investigative Dermatology, Vol. 128, No. 8, 08.2008, p. 1940-1949.

    Research output: Contribution to journalArticle

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    AU - al Yacoub, Nadya

    AU - Romanowska, Malgorzata

    AU - Krauss, Sybille

    AU - Schweiger, Susann

    AU - Foerster, John

    PY - 2008/8

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    N2 - Peroxisome proliferator-activated receptor beta/delta (PPAR delta) is a nuclear hormone receptor regulating diverse biological processes, including beta-oxidation of fatty acid and epithelial cell differentiation. To date, the role of PPAR delta in the immune system has not been thoroughly studied. Here, we show that PPAR delta is expressed in activated human T cells purified from peripheral blood as well as in T cells isolated from affected psoriasis skin lesions. PPAR delta is induced in T cells on stimulation with type 1 IFN. Functionally, PPAR delta enhances proliferation of primary T cells and blocks apoptosis induced by type 1 IFN and by serum deprivation. We show that these cellular functions are mediated by the activation of extracellular signal-regulated kinase1/2 signaling. Our results (1) establish a direct molecular link between type 1 IFN signaling and PPAR delta, (2) define a functional role for PPAR delta in human T cells, and (3) suggest that the induction of PPAR delta by type 1 IFN contributes to the persistence of activated T cells in psoriasis skin lesions.

    AB - Peroxisome proliferator-activated receptor beta/delta (PPAR delta) is a nuclear hormone receptor regulating diverse biological processes, including beta-oxidation of fatty acid and epithelial cell differentiation. To date, the role of PPAR delta in the immune system has not been thoroughly studied. Here, we show that PPAR delta is expressed in activated human T cells purified from peripheral blood as well as in T cells isolated from affected psoriasis skin lesions. PPAR delta is induced in T cells on stimulation with type 1 IFN. Functionally, PPAR delta enhances proliferation of primary T cells and blocks apoptosis induced by type 1 IFN and by serum deprivation. We show that these cellular functions are mediated by the activation of extracellular signal-regulated kinase1/2 signaling. Our results (1) establish a direct molecular link between type 1 IFN signaling and PPAR delta, (2) define a functional role for PPAR delta in human T cells, and (3) suggest that the induction of PPAR delta by type 1 IFN contributes to the persistence of activated T cells in psoriasis skin lesions.

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    KW - GROWTH-FACTOR

    KW - NUCLEAR RECEPTOR

    KW - GAMMA AGONISTS

    KW - INDUCE APOPTOSIS

    KW - DENDRITIC CELLS

    KW - LYMPHOCYTES

    KW - EXPRESSION

    KW - BINDING

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