The Transcription Factor EB Links Cellular Stress to the Immune Response

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B cell Molecular Immunology Section, Laboratory of Immunoregulation, National Institutes of Allergy and Infection Disease, National Institutes of Health, Bethesda, MD. Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Solna, Sweden.

The Yale journal of biology and medicine. 2017;(2):301-315
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Abstract

The transcription factor EB (TFEB) is the master transcriptional regulator of autophagy and lysosome biogenesis. Recent advances have led to a paradigm shift in our understanding of lysosomes from a housekeeping cellular waste bin to a dynamically regulated pathway that is efficiently turned up or down based on cellular needs. TFEB coordinates the cellular response to nutrient deprivation and other forms of cell stress through the lysosome system, and regulates a myriad of cellular processes associated with this system including endocytosis, phagocytosis, autophagy, and lysosomal exocytosis. Autophagy and the endolysosomal system are critical to both the innate and adaptive arms of the immune system, with functions in effector cell priming and direct pathogen clearance. Recent studies have linked TFEB to the regulation of the immune response through the endolysosmal pathway and by direct transcriptional activation of immune related genes. In this review, we discuss the current understanding of TFEB's function and the molecular mechanisms behind TFEB activation. Finally, we discuss recent advances linking TFEB to the immune response that positions lysosomal signaling as a potential target for immune modulation.

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Publication Type : Review

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