Evidence map›Paper›PMID 25012165›Full record

ArticleJournal of the American Society of Nephrology : JASN2015

Renal F4/80+ CD11c+ mononuclear phagocytes display phenotypic and functional characteristics of macrophages in health and in adriamycin nephropathy.

Qi Cao, Yiping Wang, Xin Maggie Wang, Junyu Lu, Vincent W S Lee, Qianling Ye, Hanh Nguyen, Guoping Zheng, Ye Zhao, Stephen I Alexander and 1 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

63 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
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  7. CXInflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
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  19. Renal CD169Life science alliance · 2021
    Article
  20. Review

3 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 2 countries.

Qi CaoCentre for Transplant and Renal Research and qi.cao@sydney.edu.au.
Yiping WangCentre for Transplant and Renal Research and.
Xin Maggie WangFlow Cytometry Facility, Westmead Millennium Institute, University of Sydney, Sydney, New South Wales, Australia; and.
Junyu LuCentre for Transplant and Renal Research and.
Vincent W S LeeCentre for Transplant and Renal Research and.
Qianling YeCentre for Transplant and Renal Research and.
Hanh NguyenCentre for Transplant and Renal Research and.
Guoping ZhengCentre for Transplant and Renal Research and.
Ye ZhaoCentre for Transplant and Renal Research and.
Stephen I AlexanderCentre for Kidney Research, Children's Hospital at Westmead, Sydney, New South Wales, Australia.
David C H HarrisCentre for Transplant and Renal Research and.
Metabolism and Renal Physiology · FRWestmead Institute · AUChildren's Hospital at Westmead · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conventional markers of macrophages (Mфs) and dendritic cells (DCs) lack specificity and often overlap, leading to confusion and controversy regarding the precise function of these cells in kidney and other diseases. This study aimed to identify the phenotype and function of renal mononuclear phagocytes (rMPs) expressing key markers of both Mфs and DCs. F4/80(+)CD11c(+) cells accounted for 45% of total rMPs in normal kidneys and in those from mice with Adriamycin nephropathy (AN). Despite expression of the DC marker CD11c, these double-positive rMPs displayed the features of Mфs, including Mф-like morphology, high expression of CD68, CD204, and CD206, and high phagocytic ability but low antigen-presenting ability. F4/80(+)CD11c(+) cells were found in the cortex but not in the medulla of the kidney. In AN, F4/80(+)CD11c(+) cells displayed an M1 Mф phenotype with high expression of inflammatory mediators and costimulatory factors. Adoptive transfer of F4/80(+)CD11c(+) cells separated from diseased kidney aggravated renal injury in AN mice. Furthermore, adoptive transfer of common progenitors revealed that kidney F4/80(+)CD11c(+) cells were derived predominantly from monocytes, but not from pre-DCs. In conclusion, renal F4/80(+)CD11c(+) cells are a major subset of rMPs and display Mф-like phenotypic and functional characteristics in health and in AN.

Indexed as

PhenotypeAdoptive TransferAnimalsAntigens, CDAntigens, DifferentiationAntigens, Differentiation, MyelomonocyticBiomarkersCD11 AntigensCD68 MoleculeDisease Models, AnimalDoxorubicinIn Vitro TechniquesKidneyKidney DiseasesLectins, C-TypeMacrophagesAntigens, CDAntigens, DifferentiationAntigens, Differentiation, MyelomonocyticBiomarkersCD11 AntigensCD68 antigen, humanCD68 MoleculeDoxorubicinLectins, C-TypeMannose-Binding LectinsMannose Receptormonocyte-macrophage differentiation antigenMsr1 protein, mouseReceptors, Cell SurfaceScavenger Receptors, Class ACKDdendritic cellsmacrophagesrenal mononuclear phagocytes

Identifiers

PMID25012165
PMCPMC4310657
OpenAlexW2132981330

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.