Evidence map›Paper›PMID 32385245›Full record

ArticleNature communications2020

Distinct fate, dynamics and niches of renal macrophages of bone marrow or embryonic origins.

Fengming Liu, Shen Dai, Dechun Feng, Zhongnan Qin, Xiao Peng, Siva S V P Sakamuri, Mi Ren, Li Huang, Min Cheng, Kabir E Mohammad and 15 more

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing 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

77 citing papers in PubMed.

  1. Review
  2. Macrophage-Fibroblast Crosstalk in Kidney Injury: A Narrative Review.International journal of molecular sciences · 2026
    Review
  3. Review
  4. Article
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  19. Article
  20. Article

17 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

25 authors.

Fengming LiuDivision of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, 70433, USA. fliu6@tulane.edu.ORCID http://orcid.org/0000-0002-8815-3356
Shen DaiDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Dechun FengLaboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, USA.
Zhongnan QinDivision of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, 70433, USA.
Xiao PengDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Siva S V P SakamuriDepartment of Pharmacology, Tulane University School of Medicine, 1430 Tulane Avenue, New Orleans, LA, 70112, USA.
Mi RenDivision of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, 70433, USA.
Li HuangDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Min ChengDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Kabir E MohammadDivision of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, 70433, USA.
Ping QuDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Yong ChenDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Chunling ZhaoDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Faliang ZhuDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Shujian LiangDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Bertal H AktasDepartment of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-7829-4553
Xiaofeng YangCenter for Metabolic Disease Research and Cardiovascular Research, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Hong WangCenter for Metabolic Disease Research and Cardiovascular Research, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Prasad V G KatakamDepartment of Pharmacology, Tulane University School of Medicine, 1430 Tulane Avenue, New Orleans, LA, 70112, USA.ORCID http://orcid.org/0000-0002-4708-9140
David W BusijaDepartment of Pharmacology, Tulane University School of Medicine, 1430 Tulane Avenue, New Orleans, LA, 70112, USA.
Tracy FischerDivision of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, 70433, USA.ORCID http://orcid.org/0000-0003-4859-3776
Prasun K DattaDepartment of Neuroscience, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Jay RappaportDivision of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, 70433, USA.
Bin GaoLaboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, USA.
Xuebin QinDivision of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, 70433, USA. xqin2@tulane.edu.ORCID http://orcid.org/0000-0001-9875-983X

Funding

Tulane NPRC SPF Sheltered Outdoor Enclosure ExpansionP51OD011104 · OD · TULANE UNIVERSITY OF LOUISIANA · PI L Lee HAMM · 2012 to 2026
$142.4M
Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
The role of the CMV-associated reactive oxygen species in age-relatedP20GM103629 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI JAZWINSKI, S MICHAL · 2012 to 2021
$22.4M
Molecular mechanisms of liver injury, repair, and immunityZIAAA000368 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GAO, BIN · 2009 to 2023
$16.1M
Project 3 Dysregulation of metabolic communication of oligodendrocytes and neurons by cocaine and TatP01DA037830 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI KHALILI, KAMEL · 2015 to 2019
$7.4M
Interdisciplinary And Translational Research Training In NeurohivT32MH079785 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI Kamel Khalili · 2008 to 2026
$5.4M
CD40 monocyte in chronic kidney diseaseR01DK113775 · NIDDK · TEMPLE UNIV OF THE COMMONWEALTH · PI WANG, HONG · 2017 to 2021
$3.3M
The roles of miR-155 in regulating atherosclerosis and metabolically healthy obesityR01HL138749 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI YANG, XIAOFENG · 2017 to 2020
$2.6M
Mitochondrial structure and function in cerebral arteries during diabetes and ischemic stressR01HL148836 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI BUSIJA, DAVID W · 2020 to 2023
$2.6M
IL-35 inhibits gut microbiota-produced uremic toxin-accelerated endothelial cell activationR01HL147565 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI YANG, XIAOFENG · 2019 to 2022
$2.6M
Role of caspase-1 activation in HIV-1 associated atherogenesisR01HL141132 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI BURDO, TRICIA HELEN, QIN, XUEBIN · 2018 to 2021
$2.5M
Atherogenic roles of complement systemR01HL130233 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI QIN, XUEBIN, WANG, HONG · 2016 to 2019
$2.5M
NHLBI NIH HHS R01 HL130233NHLBI NIH HHS R01 HL138749NHLBI NIH HHS R01 HL141132NHLBI NIH HHS R01 HL147565NHLBI NIH HHS R01 HL148836NIA NIH HHS R21 AG063345NIDA NIH HHS P01 DA037830NIDDK NIH HHS R01 DK113775NIGMS NIH HHS P20 GM103629NIGMS NIH HHS U54 GM104940NIH HHS P51 OD011104NIH HHS R21 OD024931NIMH NIH HHS T32 MH079785NINDS NIH HHS R01 NS094834
6 · The paper itself

Abstract

Renal macrophages (RMs) participate in tissue homeostasis, inflammation and repair. RMs consist of embryo-derived (EMRMs) and bone marrow-derived RMs (BMRMs), but the fate, dynamics, replenishment, functions and metabolic states of these two RM populations remain unclear. Here we investigate and characterize RMs at different ages by conditionally labeling and ablating RMs populations in several transgenic lines. We find that RMs expand and mature in parallel with renal growth after birth, and are mainly derived from fetal liver monocytes before birth, but self-maintain through adulthood with contribution from peripheral monocytes. Moreover, after the RMs niche is emptied, peripheral monocytes rapidly differentiate into BMRMs, with the CX3CR1/CX3CL1 signaling axis being essential for the maintenance and regeneration of both EMRMs and BMRMs. Lastly, we show that EMRMs have a higher capacity for scavenging immune complex, and are more sensitive to immune challenge than BMRMs, with this difference associated with their distinct glycolytic capacities.

Indexed as

Cell LineageAnimalsBone Marrow CellsChemokine CX3CL1CX3C Chemokine Receptor 1FemaleFetusKidneyLiverMacrophagesMaleMiceMonocytesChemokine CX3CL1CX3C Chemokine Receptor 1Cx3cl1 protein, mouseCx3cr1 protein, mouse

Identifiers

PMID32385245
PMCPMC7210253

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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.