Evidence map›Paper›PMID 27546006›Full record

ArticleActa pharmacologica Sinica2016

Intestinal Metrnl released into the gut lumen acts as a local regulator for gut antimicrobial peptides.

Zhi-Yong Li, Mao-Bing Fan, Sai-Long Zhang, Yi Qu, Si-Li Zheng, Jie Song, Chao-Yu Miao

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Metrnl in mitigating radiation enteritisActa pharmaceutica Sinica. B · 2026
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  4. Metrnl in health and disease: tissue-specific actions and signaling networks.Apoptosis : an international journal on programmed cell death · 2026
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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

7 authors at 1 institution in 1 country.

Zhi-Yong LiDepartment of Pharmacology, Second Military Medical University, Shanghai 200433, China.
Mao-Bing FanDepartment of Pharmacology, Second Military Medical University, Shanghai 200433, China.
Sai-Long ZhangDepartment of Pharmacology, Second Military Medical University, Shanghai 200433, China.
Yi QuDepartment of Pharmacology, Second Military Medical University, Shanghai 200433, China.
Si-Li ZhengDepartment of Pharmacology, Second Military Medical University, Shanghai 200433, China.
Jie SongDepartment of Pharmacology, Second Military Medical University, Shanghai 200433, China.
Chao-Yu MiaoDepartment of Pharmacology, Second Military Medical University, Shanghai 200433, China.
Second Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimMetrnl is a novel secreted protein, but its physiological roles remain elusive. In this study, we investigated the tissue expression pattern of Metrnl in humans and explored its possible physiological role in the tissues with most highly expressed levels.

methodsA human tissue microarray containing 19 types of tissues from 69 donors was used to examine the tissue expression pattern of Metrnl, and the expression pattern was further verified in fresh human and mouse tissues. Intestinal epithelial cell-specific Metrnl knockout mice were generated, which were used to analyze the physiological roles of Metrnl.

resultsMetrnl was the most highly expressed in the human gastrointestinal tract, and was specifically expressed in the intestinal epithelium. Consistent with this, Metrnl mRNA was also most highly expressed in the mouse gastrointestinal tract among the 14 types of tissues tested. In the intestinal epithelial cell-specific Metrnl knockout mice, the Metrnl levels in the gut fluid were significantly reduced, whereas the Metrnl serum levels showed a trend towards a reduction, but this change was not statistically significant. This cell-specific deletion of Metrnl did not affect body weight, food intake, blood glucose, colon length and histology, intestinal permeability, mucus content or mucin 2 expression under physiological conditions, but statistically decreased the expression of antimicrobial peptides, such as regenerating islet-derived 3 gamma (Reg3g) and lactotransferrin.

conclusionMetrnl is highly expressed in the intestinal epithelial cells of humans and mice, which mainly contributes to the local gut Metrnl levels and affects the serum Metrnl level to a lesser extent. Metrnl plays a role in maintaining gut antimicrobial peptides.

Indexed as

AdipokinesAdultAgedAnimalsAntimicrobial Cationic PeptidesColonEpithelial CellsFemaleHumansIntestinal MucosaLactoferrinMaleMice, KnockoutMiddle AgedNerve Growth FactorsOrgan SpecificityAdipokinesAntimicrobial Cationic Peptidescometin protein, mouseLactoferrinMetrnl protein, humanNerve Growth FactorsPancreatitis-Associated ProteinsProteinsReg3b protein, mouseReg3g protein, mouseSaa3 protein, mouseSerum Amyloid A Protein

Identifiers

PMID27546006
PMCPMC5099411
OpenAlexW2513799135

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.