Dnmt3a restrains mast cell inflammatory responses.

Leoni, Cristina; Montagner, Sara; Rinaldi, Andrea; Bertoni, Francesco; Polletti, Sara; Balestrieri, Chiara; Monticelli, Silvia (2017). Dnmt3a restrains mast cell inflammatory responses. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 114(8), E1490-E1499. National Academy of Sciences NAS 10.1073/pnas.1616420114

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DNA methylation and specifically the DNA methyltransferase enzyme DNMT3A are involved in the pathogenesis of a variety of hematological diseases and in regulating the function of immune cells. Although altered DNA methylation patterns and mutations in DNMT3A correlate with mast cell proliferative disorders in humans, the role of DNA methylation in mast cell biology is not understood. By using mast cells lacking Dnmt3a, we found that this enzyme is involved in restraining mast cell responses to acute and chronic stimuli, both in vitro and in vivo. The exacerbated mast cell responses observed in the absence of Dnmt3a were recapitulated or enhanced by treatment with the demethylating agent 5-aza-2'-deoxycytidine as well as by down-modulation of Dnmt1 expression, further supporting the role of DNA methylation in regulating mast cell activation. Mechanistically, these effects were in part mediated by the dysregulated expression of the scaffold protein IQGAP2, which is characterized by the ability to regulate a wide variety of biological processes. Altogether, our data demonstrate that DNMT3A and DNA methylation are key modulators of mast cell responsiveness to acute and chronic stimulation.

Item Type:

Journal Article (Original Article)

Graduate School:

Graduate School for Cellular and Biomedical Sciences (GCB)

ISSN:

0027-8424

Publisher:

National Academy of Sciences NAS

Language:

English

Submitter:

Marlene Wolf Tobler

Date Deposited:

30 Nov 2017 11:50

Last Modified:

24 Oct 2019 05:09

Publisher DOI:

10.1073/pnas.1616420114

PubMed ID:

28167789

Uncontrolled Keywords:

DNA methylation epigenetics inflammation mast cells

BORIS DOI:

10.7892/boris.106743

URI:

https://boris.unibe.ch/id/eprint/106743

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