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The PRKAA1/AMPKα1 pathway triggers autophagy during CSF1-induced human monocyte differentiation and is a potential target in CMML

par Obba, Sandrine;Marchetti, Sandrine;Rocchi, Stephane;Droin, Nathalie;Cluzeau, Thomas;Robert, Guillaume;Luciano, Frederic;Robaye, Bernard ;Foretz, Marc;Viollet, Benoit;Legros, Laurence;Hizir, Zoheir;Solary, Éric;Auberger, Patrick;Jacquel, Arnaud;Boyer, Laurent;Selimoglu-Buet, Dorothée;Pfeifer, Anja;Michel, Gregory;Hamouda, Mohamed Amine;Gonçalvés, Diogo;Cerezo, Michael
Référence Autophagy, 11, 7, page (1114-1129)
Publication Publié, 2015-01

Article révisé par les pairs

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Résumé :

Autophagy is induced during differentiation of human monocytes into macrophages that is mediated by CSF1/CSF- 1/M-CSF (colony stimulating factor 1 [macrophage]). However, little is known about the molecular mechanisms that link CSF1 receptor engagement to the induction of autophagy. Here we show that the CAMKK2-PRKAA1-ULK1 pathway is required for CSF1-induced autophagy and human monocyte differentiation. We reveal that this pathway links P2RY6 to the induction of autophagy, and we decipher the signaling network that links the CSF1 receptor to P2RY6-mediated autophagy and monocyte differentiation. In addition, we show that the physiological P2RY6 ligand UDP and the specific P2RY6 agonist MRS2693 can restore normal monocyte differentiation through reinduction of autophagy in primary myeloid cells from some but not all chronic myelomonocytic leukemia (CMML) patients. Collectively, our findings highlight an essential role for PRKAA1-mediated autophagy during differentiation of human monocytes and pave the way for future therapeutic interventions for CMML.