Evidence map›Paper›PMID 35048969›Full record

ArticleCardiovascular research2022

The role of immunoglobulin E and mast cells in hypertension.

Weipeng Ge, Xiaoxiao Guo, Xiaomin Song, Junling Pang, Xuan Zou, Yonglin Liu, Yongliang Niu, Zhengqing Li, Hongmei Zhao, Ran Gao and 1 more

Abstract read
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In one paragraph

Article in Cardiovascular research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
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

22 citing papers in PubMed, 15 citations in OpenAlex.

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  16. Impact ofFrontiers in gastroenterology (Lausanne, Switzerland) · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Weipeng GeDepartment of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Dongdansantiao 5, Dongcheng District, Beijing 100730, China.
Xiaoxiao GuoDepartment of Cardiology, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.ORCID 0000-0002-8583-5992
Xiaomin SongDepartment of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Dongdansantiao 5, Dongcheng District, Beijing 100730, China.
Junling PangDepartment of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Dongdansantiao 5, Dongcheng District, Beijing 100730, China.ORCID 0000-0002-5866-311X
Xuan ZouDepartment of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Dongdansantiao 5, Dongcheng District, Beijing 100730, China.
Yonglin LiuShenmu Hospital, The Affiliated Shenmu Hospital of Northwest University, Shaanxi Province, Shenmu 719300, China.ORCID 0000-0001-8748-9846
Yongliang NiuShenmu Hospital, The Affiliated Shenmu Hospital of Northwest University, Shaanxi Province, Shenmu 719300, China.
Zhengqing LiShenmu Hospital, The Affiliated Shenmu Hospital of Northwest University, Shaanxi Province, Shenmu 719300, China.
Hongmei ZhaoDepartment of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Dongdansantiao 5, Dongcheng District, Beijing 100730, China.
Ran GaoDepartment of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Dongdansantiao 5, Dongcheng District, Beijing 100730, China.
Jing WangDepartment of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Dongdansantiao 5, Dongcheng District, Beijing 100730, China.ORCID 0000-0003-2410-5408
Chinese Academy of Medical Sciences & Peking Union Medical College · CNSheng Jing Hospital · CNPeking Union Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsHypertension is the major cause of cardiovascular diseases and global mortality. Immunoglobulin E (IgE), which plays crucial roles in allergic diseases, has been implicated in the pathogenesis of vascular and cardiac remodelling via its receptor (FcεR1). In this study, we aimed to reveal the role of IgE and FcεR1 in hypertension. METHODS AND

resultsHerein, we reported that IgE levels were significantly increased in hypertensive patients as well as in hypertensive mice induced by angiotensin II (Ang II). Ang II-induced vascular remodelling and hypertension were significantly alleviated in FcεR1 genetic knockout mice or in mice treated with anti-IgE monoclonal antibody. Similarly, treatment with omalizumab (a clinical IgE antagonist) also markedly inhibited Ang II-induced hypertension. Furthermore, the cellular contribution of IgE-FcεR1 in hypertension was evaluated in mice with FcεR1 conditional knockout in mast cell (MC), smooth muscle cell (SMC), or endothelial cell (EC). Our data revealed that IgE-mediated hypertension is largely dependent on FcεR1 in MCs but not SMCs and ECs. Finally, RNA-seq and signalling pathway analyses of mouse bone marrow-derived MCs suggested that interleukin 6 (IL-6) is one of critical mediators in IgE-mediated hypertension. IL-6 derived from IgE-stimulated MCs promoted reactive oxygen species production and decreased the levels of phosphorylated endothelial nitric oxide synthase in ECs, leading to endothelial dysfunction.

conclusionOur findings reveal that IgE contributes to the pathogenesis of hypertension, at least partially through activating the IgE-FcεR1 signalling in MCs. Thus, IgE may represent a new therapeutic target for IgE-mediated hypertension.

Indexed as

HypertensionMast CellsAnimalsImmunoglobulin EInterleukin-6MiceMice, KnockoutReceptors, IgEImmunoglobulin EInterleukin-6Receptors, IgEHypertensionIgEIL-6Mast cellROS

Identifiers

PMID35048969
OpenAlexW4206214290

What OpenQuestion holds

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Registered trials

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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.