Abstract

Transcription factor EB (TFEB) is a member of the microphthalmia-associated transcription factor/transcription factor E (MiTF/TFE) family and critically involved in the maintenance of structural integrity and functional balance of multiple cells. In this review, we described the effects of post-transcriptional modifications, including phosphorylation, acetylation, SUMOylation, and ubiquitination, on the subcellular localization and activation of TFEB. The activated TFEB enters into the nucleus and induces the expressions of targeted genes. We then presented the role of TFEB in the biosynthesis of multiple organelles, completion of lysosome-autophagy pathway, metabolism regulation, immune, and inflammatory responses. This review compiles existing knowledge in the understanding of TFEB regulation and function, covering its essential role in response to cellular stress. We further elaborated the involvement of TFEB dysregulation in the pathophysiological process of various diseases, such as the catabolic hyperactivity in tumors, the accumulation of abnormal aggregates in neurodegenerative diseases, and the aberrant host responses in inflammatory diseases. In this review, multiple drugs have also been introduced, which enable regulating the translocation and activation of TFEB, showing beneficial effects in mitigating various disease models. Therefore, TFEB might serve as a potential therapeutic target for human diseases. The limitation of this review is that the mechanism of TFEB-related human diseases mainly focuses on its association with lysosome and autophagy, which needs deep description of other mechanism in diseases progression after getting more advanced information.

Highlights

  • Transcription factor EB (TFEB) belongs to the microphthalmia-associated transcription factor/transcription factor E (MiTF/TFE) family, which transcriptionally regulates the expression of multiple genes in response to various stimuli (Napolitano and Ballabio, 2016)

  • Autophagy refers to a tight regulated process that transports a variety of cellular components to lysosomes for degradation, which involves the renewal of multiple organelles and the removal of misfolded proteins and even invaded intracellular pathogens

  • Since TFEB is essential for maintaining the stability of cellular structure and function, the dysregulation of TFEB activity appears to be associated with the occurrence and development of various human diseases, such as tumors, neurodegenerative diseases, and inflammatory diseases, implying the modulation of TFEB a potential therapeutic target (Table 1)

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Summary

INTRODUCTION

Transcription factor EB (TFEB) belongs to the microphthalmia-associated transcription factor/transcription factor E (MiTF/TFE) family, which transcriptionally regulates the expression of multiple genes in response to various stimuli (Napolitano and Ballabio, 2016). In addition to TFEB, other transcription factors have been identified belonging to the MiTF/TFE family, including MiTF, transcription factor EC (TFEC), and transcription factor E3 (TFE3) (Napolitano and Ballabio, 2016; Slade and Pulinilkunnil, 2017) These factors share the similar domains for efficient transcription: the basic domain for DNA binding, and the helixloop-helix as well as leucine zipper (BHLH-LZ) domains which serve as the formation sites for homodimers or heterodimers in association with the other family members (Aksan and Goding, 1998).

THE REGULATION OF TFEB ACTIVITY
The Phosphorylation of Cytoplasmic TFEB
Nuclear Transfer of TFEB by Dephosphorylation
THE FUNCTION OF TFEB
The Effects of TFEB on Biosynthesis and Function of Multiple Organelles
Regulatory Impacts on Autophagy
Immune and Inflammatory Responses
THE ROLE OF TFEB IN HUMAN DISEASES
Activation of TFEB reverses lysosomal dysfunction and reduces oxidative stress
Inflammatory Diseases
Neurodegenerative Diseases
CONCLUSION AND PERSPECTIVE
Findings
AUTHOR CONTRIBUTIONS
Full Text
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