Evidence map›Paper›PMID 31571584›Full record

ArticleeLife2019

Hemozoin produced by mammals confers heme tolerance.

Rini H Pek, Xiaojing Yuan, Nicole Rietzschel, Jianbing Zhang, Laurie Jackson, Eiji Nishibori, Ana Ribeiro, William Simmons, Jaya Jagadeesh, Hiroshi Sugimoto and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. An extended network for regulation of heme homeostasis in cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Article
  8. Heme and immunity: The heme oxygenase dichotomy.Journal of inorganic biochemistry · 2025
    Review
  9. Identification of a divalent metal transporter required for cellular iron metabolism in malaria parasites.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Update on heme biosynthesis, tissue-specific regulation, heme transport, relation to iron metabolism and cellular energy.Liver international : official journal of the International Association for the Study of the Liver · 2024
    Review
  11. Article
  12. Article
  13. Heme (dys)homeostasis and liver disease.Frontiers in physiology · 2024
    Review
  14. Review
  15. FDX1-dependent and independent mechanisms of elesclomol-mediated intracellular copper delivery.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Molecular Mechanisms of Iron and Heme Metabolism.Annual review of nutrition · 2022
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 2 countries.

Rini H PekDepartment of Animal and Avian Sciences, University of Maryland, College Park, United States.ORCID https://orcid.org/0000-0002-2570-7534
Xiaojing YuanDepartment of Animal and Avian Sciences, University of Maryland, College Park, United States.ORCID http://orcid.org/0000-0002-0969-5748
Nicole RietzschelDepartment of Animal and Avian Sciences, University of Maryland, College Park, United States.
Jianbing ZhangDepartment of Animal and Avian Sciences, University of Maryland, College Park, United States.
Laurie JacksonDepartment of Medicine, University of Utah School of Medicine, Salt Lake City, United States.
Eiji NishiboriFaculty of Pure and Applied Sciences, University of Tsukuba, Tsukuba, Japan.
Ana RibeiroDepartment of Animal and Avian Sciences, University of Maryland, College Park, United States.
William SimmonsGenetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, United States.
Jaya JagadeeshGenetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, United States.
Hiroshi SugimotoRIKEN SPring-8 Center, Sayo, Hyogo, Japan.ORCID http://orcid.org/0000-0002-3140-8362
Md Zahidul AlamDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, United States.
Lisa GarrettNHGRI Embryonic Stem Cell and Transgenic Mouse Core, National Human Genome Research Institute, National Institutes of Health, Bethesda, United States.
Malay HaldarDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, United States.
Martina RalleDepartment of Molecular and Medical Genetics, Oregon Health and Science University, Portland, United States.
John D PhillipsDepartment of Medicine, University of Utah School of Medicine, Salt Lake City, United States.
David M BodineGenetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, United States.
Iqbal HamzaDepartment of Animal and Avian Sciences, University of Maryland, College Park, United States.ORCID https://orcid.org/0000-0003-0045-0610
University of Maryland, College Park · USNational Institutes of Health · USUniversity of Pennsylvania · USUniversity of Utah · USOregon Health & Science University · USSPring-8 · JPUniversity of Tsukuba · JP

Funding

Proteomics CoreU54DK110858 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Anna E Beaudin, JAMES Eric COX · 2016 to 2026
$8.6M
The Transport of Nutritional Heme in Animal DevelopmentR01DK085035 · NIDDK · UNIV OF MARYLAND, COLLEGE PARK · PI HAMZA, IQBAL · 2010 to 2019
$3.6M
Imaging heme based mitochondrial-cell signaling networks in cell and animal modelR33ES025661 · NIEHS · GEORGIA INSTITUTE OF TECHNOLOGY · PI REDDI, AMIT RAM · 2017 to 2019
$1.7M
Training Program in Cell & Molecular BiologyT32GM080201 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI DELWICHE, CHARLES F · 2009 to 2019
$1.6M
Imaging heme based mitochondrial-cell signaling networks in cell and animal models of heavy metal toxicityR21ES025661 · NIEHS · GEORGIA INSTITUTE OF TECHNOLOGY · PI REDDI, AMIT RAM · 2015 to 2016
$416k
Department of Energy DE-AC02-06CH11357Japan Synchrotron Radiation Research Institute 2017A0074NHGRI NIH HHS IntramuralNIDDK NIH HHS DK085035NIDDK NIH HHS DK110858NIDDK NIH HHS R01 DK085035NIDDK NIH HHS U54 DK110858NIEHS NIH HHS ES025661NIEHS NIH HHS R21 ES025661NIEHS NIH HHS R33 ES025661NIGMS NIH HHS T32 GM080201
6 · The paper itself

Abstract

Free heme is cytotoxic as exemplified by hemolytic diseases and genetic deficiencies in heme recycling and detoxifying pathways. Thus, intracellular accumulation of heme has not been observed in mammalian cells to date. Here we show that mice deficient for the heme transporter SLC48A1 (also known as HRG1) accumulate over ten-fold excess heme in reticuloendothelial macrophage lysosomes that are 10 to 100 times larger than normal. Macrophages tolerate these high concentrations of heme by crystallizing them into hemozoin, which heretofore has only been found in blood-feeding organisms.

Indexed as

AnimalsHemeHeme Oxygenase-1HemeproteinsMacrophagesMembrane ProteinsMiceHemeHeme Oxygenase-1HemeproteinshemozoinHmox1 protein, mouseHRG-1 protein, mouseMembrane Proteinsanemiabiochemistrycell biologychemical biologyhemehemozoinironlysosomemacrophagesmouse

Identifiers

PMID31571584
PMCPMC6773446
OpenAlexW2978160564

What OpenQuestion holds

Textmetadata
LicenceCC0
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.