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10.1016/j.cytogfr.2016.03.008

http://scihub22266oqcxt.onion/10.1016/j.cytogfr.2016.03.008
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C4899287!4899287!27068414
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suck abstract from ncbi


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pmid27068414      Cytokine+Growth+Factor+Rev 2016 ; 29 (ä): 17-22
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  • Beyond autophagy: New roles for ULK1 in immune signaling and interferon responses #MMPMID27068414
  • Saleiro D; Kosciuczuk EM; Platanias LC
  • Cytokine Growth Factor Rev 2016[Jun]; 29 (ä): 17-22 PMID27068414show ga
  • The human serine/threonine kinase ULK1 is the human homolog of the Caenorhabditis elegans Unc-51 kinase and of the Saccharomyces cerevisiae autophagy-related protein kinase Atg1. As Unc-51 and Atg1, ULK1 regulates both axon growth and autophagy, respectively, in mammalian cells. However, a novel immunoregulatory role of ULK1 has been recently described. This kinase was shown to be required for regulation of both type I interferon (IFN) production and induction of type I IFN signaling. Optimal regulation of IFN production is crucial for generation of effective IFN-immune responses, and defects in such networks can be detrimental for the host leading to uncontrolled pathogen infection, tumor growth, or autoimmune diseases. Thus, ULK1 plays a central role in IFN-dependent immunity. Here we review the diverse roles of ULK1, with special focus on its importance to type I IFN signaling, and highlight important future study questions.
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