Evidence map›Paper›PMID 42675151›Full record

ArticleNature metabolism2026

Neutrophil serine proteases inhibit thermogenic capacity of visceral white adipose tissue.

Lufengzi Yuan, Xiaoping Wu, Jiuyu Zong, Mengxue Jiang, Sanxing Gao, Zixuan Zhang, Xiaowen Huang, Manyu Zhu, Minqi Xiang, Lin Wang and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature metabolism, 2026. 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. Article
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

15 authors.

Lufengzi YuanThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Xiaoping WuThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Jiuyu ZongThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Mengxue JiangThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Sanxing GaoDepartment of Pharmacology and Pharmacy, The University of Hong Kong, Hong Kong, China.ORCID http://orcid.org/0000-0001-5284-0034
Zixuan ZhangThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Xiaowen HuangThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Manyu ZhuDepartment of Pathology, Johns Hopkins University, Baltimore, MD, USA.ORCID http://orcid.org/0009-0004-3492-4305
Minqi XiangThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Lin WangSchool of Biomedical Sciences, The University of Hong Kong, Hong Kong, China.
Zhihui PingThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Yong PanDepartment of Pathophysiology, School of Basic Medical Sciences, Shenzhen University, Shenzhen, China.
Dewei YeInstitute of Metabolic Science, Science and Technology Innovation Centre, Guangzhou University of Chinese Medicine, Guangzhou, China.
Aimin XuThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.ORCID http://orcid.org/0000-0002-0668-033X
Ruby Lai Chong HooThe State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China. rubyhoo@hku.hk.ORCID http://orcid.org/0000-0001-9633-7078

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils and neutrophil-derived serine proteases (NSPs), including neutrophil elastase (NE) and proteinase 3 (PR3), are present in visceral fat of individuals and rodents with obesity, yet their roles in energy metabolism remain elusive. Here we show that neutrophil infiltration and NSP activation impair visceral fat browning in response to β-adrenergic receptor stimulation or cold exposure in male mice. Genetic deletion or local pharmacological inhibition of NE with sivelestat rescued visceral fat browning and enhanced thermogenesis. Mechanistically, NE/PR3 directly suppresses beige adipogenesis by arresting cell cycle via CDK4/cyclin D1 downregulation, impairs beige adipocyte differentiation by degrading insulin-like growth factor binding protein-3, and indirectly promotes M1 macrophage polarization. Administration of sivelestat suppressed diet-induced neutrophil infiltration, enhanced cold-induced visceral fat browning and decreased visceral fat content in mice. These findings reveal an unexpected inhibitory role of NSPs in visceral fat browning and suggest the potential of repurposing sivelestat as an anti-obese drug.

Indexed as

Adipose Tissue, WhiteIntra-Abdominal FatNeutrophilsSerine ProteasesThermogenesisAnimalsMaleMiceMice, Inbred C57BLSulfonamidesSerine ProteasesSulfonamides

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.