001     277527
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024 7 _ |a 10.1016/j.immuni.2025.01.003
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024 7 _ |a 1074-7613
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024 7 _ |a 1097-4180
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037 _ _ |a DZNE-2025-00423
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Asare, Yaw
|b 0
245 _ _ |a A cis-regulatory element controls expression of histone deacetylase 9 to fine-tune inflammasome-dependent chronic inflammation in atherosclerosis.
260 _ _ |a [Cambridge, Mass.]
|c 2025
|b Cell Press
336 7 _ |a article
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520 _ _ |a Common genetic variants in a conserved cis-regulatory element (CRE) at histone deacetylase (HDAC)9 are a major risk factor for cardiovascular disease, including stroke and coronary artery disease. Given the consistency of this association and its proinflammatory properties, we examined the mechanisms whereby HDAC9 regulates vascular inflammation. HDAC9 bound and mediated deacetylation of NLRP3 in the NACHT and LRR domains leading to inflammasome activation and lytic cell death. Targeted deletion of the critical CRE in mice increased Hdac9 expression in myeloid cells to exacerbate inflammasome-dependent chronic inflammation. In human carotid endarterectomy samples, increased HDAC9 expression was associated with atheroprogression and clinical plaque instability. Incorporation of TMP195, a class IIa HDAC inhibitor, into lipoprotein-based nanoparticles to target HDAC9 at the site of myeloid-driven vascular inflammation stabilized atherosclerotic plaques, implying a lower risk of plaque rupture and cardiovascular events. Our findings link HDAC9 to atherogenic inflammation and provide a paradigm for anti-inflammatory therapeutics for atherosclerosis.
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650 _ 7 |a GWAS
|2 Other
650 _ 7 |a HDAC9
|2 Other
650 _ 7 |a NLRP3
|2 Other
650 _ 7 |a atherosclerosis
|2 Other
650 _ 7 |a cis-regulatory element
|2 Other
650 _ 7 |a inflammasome
|2 Other
650 _ 7 |a inflammation
|2 Other
650 _ 7 |a nanobiologics
|2 Other
650 _ 7 |a stroke
|2 Other
650 _ 7 |a therapeutics
|2 Other
650 _ 7 |a Histone Deacetylases
|0 EC 3.5.1.98
|2 NLM Chemicals
650 _ 7 |a Inflammasomes
|2 NLM Chemicals
650 _ 7 |a NLR Family, Pyrin Domain-Containing 3 Protein
|2 NLM Chemicals
650 _ 7 |a HDAC9 protein, human
|0 EC 3.5.1.98
|2 NLM Chemicals
650 _ 7 |a Hdac9 protein, mouse
|0 EC 3.5.1.98
|2 NLM Chemicals
650 _ 7 |a Repressor Proteins
|2 NLM Chemicals
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Atherosclerosis: genetics
|2 MeSH
650 _ 2 |a Atherosclerosis: metabolism
|2 MeSH
650 _ 2 |a Atherosclerosis: immunology
|2 MeSH
650 _ 2 |a Histone Deacetylases: metabolism
|2 MeSH
650 _ 2 |a Histone Deacetylases: genetics
|2 MeSH
650 _ 2 |a Inflammasomes: metabolism
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Inflammation: genetics
|2 MeSH
650 _ 2 |a NLR Family, Pyrin Domain-Containing 3 Protein: metabolism
|2 MeSH
650 _ 2 |a NLR Family, Pyrin Domain-Containing 3 Protein: genetics
|2 MeSH
650 _ 2 |a Repressor Proteins: metabolism
|2 MeSH
650 _ 2 |a Repressor Proteins: genetics
|2 MeSH
650 _ 2 |a Mice, Knockout
|2 MeSH
650 _ 2 |a Regulatory Sequences, Nucleic Acid: genetics
|2 MeSH
650 _ 2 |a Mice, Inbred C57BL
|2 MeSH
650 _ 2 |a Plaque, Atherosclerotic: metabolism
|2 MeSH
650 _ 2 |a Plaque, Atherosclerotic: genetics
|2 MeSH
650 _ 2 |a Gene Expression Regulation
|2 MeSH
700 1 _ |a Yan, Guangyao
|b 1
700 1 _ |a Schlegl, Christina
|b 2
700 1 _ |a Prestel, Matthias
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700 1 _ |a van der Vorst, Emiel P C
|b 4
700 1 _ |a Teunissen, Abraham J P
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700 1 _ |a Aronova, Arailym
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700 1 _ |a Tosato, Federica
|b 7
700 1 _ |a Naser, Nawraa
|b 8
700 1 _ |a Caputo, Julio
|b 9
700 1 _ |a Prevot, Geoffrey
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700 1 _ |a Azzun, Anthony
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700 1 _ |a Wefers, Benedikt
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700 1 _ |a Wurst, Wolfgang
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700 1 _ |a Schneider, Melanie
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700 1 _ |a Forne, Ignasi
|b 15
700 1 _ |a Bidzhekov, Kiril
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700 1 _ |a Naumann, Ronald
|b 17
700 1 _ |a van der Laan, Sander W
|b 18
700 1 _ |a Brandhofer, Markus
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700 1 _ |a Cao, Jiayu
|b 20
700 1 _ |a Roth, Stefan
|b 21
700 1 _ |a Malik, Rainer
|b 22
700 1 _ |a Tiedt, Steffen
|b 23
700 1 _ |a Mulder, Willem J M
|b 24
700 1 _ |a Imhof, Axel
|b 25
700 1 _ |a Liesz, Arthur
|b 26
700 1 _ |a Weber, Christian
|b 27
700 1 _ |a Bernhagen, Jürgen
|b 28
700 1 _ |a Dichgans, Martin
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773 _ _ |a 10.1016/j.immuni.2025.01.003
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