Evidence map›Paper›PMID 36189317›Full record

ArticleFrontiers in immunology2022

Clec7a expression in inflammatory macrophages orchestrates progression of acute kidney injury.

Yaqiong Wang, Xianzhe Li, Xialian Xu, Jinbo Yu, Xiaohong Chen, Xuesen Cao, Jianzhou Zou, Bo Shen, Xiaoqiang Ding

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Yaqiong WangDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xianzhe LiDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xialian XuDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jinbo YuDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xiaohong ChenDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xuesen CaoDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jianzhou ZouDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.
Bo ShenDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xiaoqiang DingDepartment of Nephrology, Zhongshan Hospital, Fudan University, Shanghai, China.
Zhongshan Hospital · CNFudan University · CNShanghai Blood Center · CNShanghai Institute of Hematology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute kidney injury (AKI) is associated with high risk of mortality, post-disease renal fibrosis, kidney dysfunction and renal failure. Renal macrophages play a key role in the pathogenesis (M1 subpopulation), healing and remodeling (M2 subpopulation) in AKI and, thus, have been a promising target for clinical treatment of AKI. Here, in a mouse renal ischemia/reperfusion injury (IRI) model for AKI, we showed that renal macrophages could be further classified into Clec7a+ M1 macrophages, Clec7a- M1 macrophages, Clec7a+ M2 macrophages and Clec7a- M2 macrophages, representing distinct macrophage populations with different functionality. Interestingly, Clec7a+ M1 macrophages exhibited potent pro-inflammatory and phagocytic effects compared to Clec7a- M1 macrophages, while Clec7a- M2 macrophages exhibited better proliferating and migrating potential, which is critical for their role in tissue repairing after injury. These data from mice were further strengthened by bioinformatics analyses using published database.

Indexed as

Acute Kidney InjuryReperfusion InjuryAnimalsFibrosisKidneyMacrophagesMiceacute kidney injury (AKI)Clec7aischemia/reperfusion injury (IRI)M1 macrophagesM2 macrophagesmacrophages

Identifiers

PMID36189317
PMCPMC9520532
OpenAlexW4296095581

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.