Evidence map›Paper›PMID 40372655›Full record

ArticleApplied biochemistry and biotechnology2025

Global Analysis of the Lysine Acetylome in Macrophages from Salt-sensitive Hypertensive Rats.

Di Xie, Yanghong Dong, Jinyu Chi, Wanlin Li, Chunnan Liu, Yang Xu, Yang Li, Jingzhi Wang, Jinfeng Wu, Rui Wang and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Applied biochemistry and biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Di Xie *Department of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Yanghong Dong *Department of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Jinyu ChiDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Wanlin LiDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Chunnan LiuDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Yang XuDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Yang LiDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Jingzhi WangDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Jinfeng WuDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Rui WangDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China.
Kelaier YangDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China. orangecoco1213@163.com.
Xinhua YinDepartment of Cardiology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, PR China. yinxinhua5063@163.com.ORCID http://orcid.org/0000-0002-5874-1448

Funding

National Natural Science Foundation of China 81570437National Natural Science Foundation of China 81800352Postdoctoral Scientific Research Development Fund of Heilongjiang Province LBH-Q18093Shenzhen excellent science and technology innovation talent training project RCBS20221008093102010Shenzhen Science and Technology Innovation Program JCYJ20220531102612027
6 · The paper itself

Abstract

Research indicates that patients with salt-sensitive (SS) hypertension experience higher morbidity and target organ damage than in patients with non-SS hypertension. Dysregulated macrophage activation has been implicated in SS hypertension development, with lysine acetylation playing a role in modulating macrophage function. However, the role of macrophage acetylation patterns in SS hypertension remains unclear. This study aimed to investigate how acetylation regulates macrophage function and its role in the pathogenesis of SS hypertension. We employed quantitative acetylation proteomics to characterize the acetylome of bone marrow-derived macrophages in Dahl SS hypertensive rats fed either a high-salt or a low-salt diet. We identified 94 hyperacetylated and 49 hypoacetylated sites on 79 and 45 proteins, respectively, in the high-salt group. Notably, acetylation levels increased at lysine 20 (K20) and K46 on histone H2B, at K56 on H3, and at K77 and K79 on H4c2. We also identified conserved acetylation motifs, analyzed their Gene Ontology terms and pathways, and explored the protein-protein interactions of these differentially acetylated proteins using bioinformatics analyses. Finally, we validated the altered acetylation of H2, H3, H4, and several metabolic proteins using immunoprecipitation and western blotting. Overall, these findings offer insights into the role of lysine acetylation in macrophages from SS hypertensive rats, revealing potential therapeutic targets.

Indexed as

HypertensionLysineMacrophagesProteomeAcetylationAnimalsHistonesMaleProteomicsRatsRats, Inbred DahlSodium Chloride, DietaryHistonesLysineProteomeSodium Chloride, DietaryHistoneLysine acetylationMacrophagesMetabolic pathwaySalt-sensitive hypertension

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.