HIPK2 directs cell type–specific regulation of STAT3 transcriptional activity in Th17 cell differentiation

Author:

Cheung Ka Lung1,Jaganathan Anbalagan1,Hu Yuan23,Xu Feihong23,Lejeune Alannah1ORCID,Sharma Rajal1,Caescu Cristina I.1ORCID,Meslamani Jamel1,Vincek Adam1,Zhang Fan1,Lee Kyung2,Zaware Nilesh1,Qayum Amina Abdul4,Ren Chunyan1ORCID,Kaplan Mark H.4,He John Cijiang2,Xiong Huabao23ORCID,Zhou Ming-Ming1ORCID

Affiliation:

1. Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029

2. Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029

3. Institute of Immunology, Icahn School of Medicine at Mount Sinai, New York, NY 10029

4. Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN 46202

Abstract

Significance STAT3 (signal transducer and activator of transcription 3) is a master transcription factor that organizes cellular responses to cytokines and growth factors and is implicated in inflammatory disorders. STAT3 is a well-recognized therapeutic target for human cancer and inflammatory disorders, but how its function is regulated in a cell type–specific manner has been a major outstanding question. We discovered that Stat3 imposes self-directed regulation through controlling transcription of its own regulator homeodomain-interacting protein kinase 2 ( Hipk2 ) in a T helper 17 (Th17) cell–specific manner. Our validation of the functional importance of the Stat3–Hipk2 axis in Th17 cell development in the pathogenesis of T cell–induced colitis in mice suggests an approach to therapeutically treat inflammatory bowel diseases that currently lack a safe and effective therapy.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

HHS | National Institutes of Health

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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