Proteomics

Dataset Information

0

A cis-regulatory element controls HDAC9 expression to fine-tune inflammasome-dependent chronic inflammation


ABSTRACT: To understand the underlying molecular mechanism of Hdac9-mediated inflammasome activation and motivated by the molecular scaffolding function of HDAC9, we pursued the hypothesis that HDAC9 may serve as a docking site for cytosolic inflammasome components thereby facilitating its rapid formation upon stimulation. We tested this by performing co-immunoprecipitation experiments coupled with mass spectrometry to assess subunits of the inflammasome that interact with HDAC9.

INSTRUMENT(S): Orbitrap Exploris 480

ORGANISM(S): Homo Sapiens (human)

SUBMITTER: Ignasi Forne  

LAB HEAD: Prof. Dr. Martin Dichgans

PROVIDER: PXD042078 | Pride | 2025-07-10

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
Groups.txt Txt
Ref7473_YA_01_20220329.raw Raw
Ref7473_YA_02_20220329.raw Raw
Ref7473_YA_03_20220329.raw Raw
Ref7473_YA_04_20220329.raw Raw
Items per page:
1 - 5 of 28
altmetric image

Publications


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  ...[more]

Similar Datasets

2023-11-25 | PXD041763 | Pride
2024-07-25 | PXD054126 | Pride
2024-04-23 | PXD051489 | Pride
2019-11-11 | PXD014857 | Pride
2023-01-14 | PXD034833 | Pride
2024-10-17 | PXD044992 | Pride
2023-06-27 | PXD038414 | Pride
2021-06-23 | PXD021899 | Pride
2024-05-16 | PXD041817 | Pride
2024-04-24 | PXD045862 | Pride