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Progranulin prevents regulatory NK cell cytotoxicity against antiviral T cells.

JCI insight (2019-09-06)
Anfei Huang, Prashant V Shinde, Jun Huang, Tina Senff, Haifeng C Xu, Cassandra Margotta, Dieter Häussinger, Thomas E Willnow, Jinping Zhang, Aleksandra A Pandyra, Jörg Timm, Sascha Weggen, Karl S Lang, Philipp A Lang
RÉSUMÉ

`NK cell-mediated regulation of antigen-specific T cells can contribute to and exacerbate chronic viral infection, but the protective mechanisms against NK cell-mediated attack on T cell immunity are poorly understood. Here, we show that progranulin (PGRN) can reduce NK cell cytotoxicity through reduction of NK cell expansion, granzyme B transcription, and NK cell-mediated lysis of target cells. Following infection with the lymphocytic choriomeningitis virus (LCMV), PGRN levels increased - a phenomenon dependent on the presence of macrophages and type I IFN signaling. Absence of PGRN in mice (Grn-/-) resulted in enhanced NK cell activity, increased NK cell-mediated killing of antiviral T cells, reduced antiviral T cell immunity, and increased viral burden, culminating in increased liver immunopathology. Depletion of NK cells restored antiviral immunity and alleviated pathology during infection in Grn-/- mice. In turn, PGRN treatment improved antiviral T cell immunity. Taken together, we identified PGRN as a critical factor capable of reducing NK cell-mediated attack of antiviral T cells.

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Human PGRN ELISA Kit, for cell culture supernatants, plasma, and serum samples