PARP9 and PARP14 cross-regulate macrophage activation via STAT1 ADP-ribosylation

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PARP9 and PARP14 cross-regulate macrophage activation via STAT1 ADP-ribosylation

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Title: PARP9 and PARP14 cross-regulate macrophage activation via STAT1 ADP-ribosylation
Author: Iwata, Hiroshi; Goettsch, Claudia; Sharma, Amitabh; Ricchiuto, Piero; Goh, Wilson Wen Bin; Halu, Arda; Yamada, Iwao; Yoshida, Hideo; Hara, Takuya; Wei, Mei; Inoue, Noriyuki; Fukuda, Daiju; Mojcher, Alexander; Mattson, Peter C.; Barabási, Albert-László; Boothby, Mark; Aikawa, Elena; Singh, Sasha A.; Aikawa, Masanori

Note: Order does not necessarily reflect citation order of authors.

Citation: Iwata, H., C. Goettsch, A. Sharma, P. Ricchiuto, W. W. B. Goh, A. Halu, I. Yamada, et al. 2016. “PARP9 and PARP14 cross-regulate macrophage activation via STAT1 ADP-ribosylation.” Nature Communications 7 (1): 12849. doi:10.1038/ncomms12849. http://dx.doi.org/10.1038/ncomms12849.
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Abstract: Despite the global impact of macrophage activation in vascular disease, the underlying mechanisms remain obscure. Here we show, with global proteomic analysis of macrophage cell lines treated with either IFNγ or IL-4, that PARP9 and PARP14 regulate macrophage activation. In primary macrophages, PARP9 and PARP14 have opposing roles in macrophage activation. PARP14 silencing induces pro-inflammatory genes and STAT1 phosphorylation in M(IFNγ) cells, whereas it suppresses anti-inflammatory gene expression and STAT6 phosphorylation in M(IL-4) cells. PARP9 silencing suppresses pro-inflammatory genes and STAT1 phosphorylation in M(IFNγ) cells. PARP14 induces ADP-ribosylation of STAT1, which is suppressed by PARP9. Mutations at these ADP-ribosylation sites lead to increased phosphorylation. Network analysis links PARP9–PARP14 with human coronary artery disease. PARP14 deficiency in haematopoietic cells accelerates the development and inflammatory burden of acute and chronic arterial lesions in mice. These findings suggest that PARP9 and PARP14 cross-regulate macrophage activation.
Published Version: doi:10.1038/ncomms12849
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095532/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:29626127
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