Cyclophilin A is required for M-CSF-dependent macrophage proliferation

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Abstract

The immunosuppressor sanglifehrin A (SfA) is a member of a family of immunophilin cyclophilin A-binding molecules and does not inhibit calcineurin activity. Sanglifehrin A inhibits M-CSF-dependent macrophage proliferation by arresting the G1 phase of the cell cycle but does not affect cell viability. This immunosuppressor exerts its action on proliferation by inactivating cyclin-dependent kinase 2 (Cdk2) activity. Moreover, c-myc expression is also repressed. In the early steps of M-CSF signaling, SfA inhibits the phosphorylation of Raf-1 and the external regulated kinases (ERK) 1/2 and mitogen-activated protein kinase phosphatase-1, which are required for proliferation. The effects of SfA are not related to a block of the proteosome activity. These data show that immunophilin contributes to M-CSF-dependent proliferation through activation of the Raf-1/MEK/ERK pathway and the regulation of Cdk activities, which is required for cell cycle progression. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Sànchez-Tilló, E., Wojciechowska, M., Comalada, M., Farrera, C., Lloberas, J., & Celada, A. (2006). Cyclophilin A is required for M-CSF-dependent macrophage proliferation. European Journal of Immunology, 36(9), 2515–2524. https://doi.org/10.1002/eji.200535270

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