Evidence map›Paper›PMID 25579427›Full record

ArticleImmunity2015

Myeloid cell-derived reactive oxygen species externally regulate the proliferation of myeloid progenitors in emergency granulopoiesis.

Hyun-Jeong Kwak, Peng Liu, Besnik Bajrami, Yuanfu Xu, Shin-Young Park, César Nombela-Arrieta, Subhanjan Mondal, Yan Sun, Haiyan Zhu, Li Chai and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 121 citations in OpenAlex.

  1. Pooled it
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  13. CHIP: a clonal odyssey of the bone marrow niche.The Journal of clinical investigation · 2024
    Review
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  18. Neutrophil sub-types in maintaining immune homeostasis during steady state, infections and sterile inflammation.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 3 countries.

Hyun-Jeong KwakDepartment of Pathology, Harvard Medical School; Department of Lab Medicine, Children's Hospital Boston; Dana-Farber/Harvard Cancer Center, Boston, MA 02115, USA.
Peng LiuThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Center for Stem Cell Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, 288 Nanjing Road, Tianjin, 300020, China.
Besnik BajramiDepartment of Pathology, Harvard Medical School; Department of Lab Medicine, Children's Hospital Boston; Dana-Farber/Harvard Cancer Center, Boston, MA 02115, USA.
Yuanfu XuThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Center for Stem Cell Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, 288 Nanjing Road, Tianjin, 300020, China.
Shin-Young ParkDepartment of Pathology, Harvard Medical School; Department of Lab Medicine, Children's Hospital Boston; Dana-Farber/Harvard Cancer Center, Boston, MA 02115, USA.
César Nombela-ArrietaDepartment of Experimental Hematology, University Hospital Zurich, Schmelzbergstrasse 12, PATH G37, 8091 Zurich, Switzerland.
Subhanjan MondalDepartment of Pathology, Harvard Medical School; Department of Lab Medicine, Children's Hospital Boston; Dana-Farber/Harvard Cancer Center, Boston, MA 02115, USA.
Yan SunDepartment of Pathology, Harvard Medical School; Department of Lab Medicine, Children's Hospital Boston; Dana-Farber/Harvard Cancer Center, Boston, MA 02115, USA.
Haiyan ZhuThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Center for Stem Cell Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, 288 Nanjing Road, Tianjin, 300020, China.
Li ChaiDepartment of Pathology, Joint Program in Transfusion Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Leslie E SilbersteinDepartment of Pathology, Harvard Medical School; Department of Lab Medicine, Children's Hospital Boston; Dana-Farber/Harvard Cancer Center, Boston, MA 02115, USA.
Tao ChengThe State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Center for Stem Cell Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, 288 Nanjing Road, Tianjin, 300020, China.
Hongbo R LuoDepartment of Pathology, Harvard Medical School; Department of Lab Medicine, Children's Hospital Boston; Dana-Farber/Harvard Cancer Center, Boston, MA 02115, USA. Electronic address: hongbo.luo@childrens.harvard.edu.
Boston Children's Hospital · USChinese Academy of Medical Sciences & Peking Union Medical College · CNBrigham and Women's Hospital · USUniversity Hospital of Zurich · CH

Funding

Transcription regulation in hematopoiesisP01HL095489 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI PARK, SHINYOUNG · 2010 to 2020
$20.1M
Enhancing neutrophil function in neutropenia-related pneumoniaR01HL092020 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI LUO, HONGBO R · 2009 to 2022
$5.2M
Regulation of neutrophil function by ROS-induced actin glutathionylationR01AI103142 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI LUO, HONGBO R · 2014 to 2018
$2.2M
NHLBI NIH HHS P01 HL095489NHLBI NIH HHS R01 HL092020NHLBI NIH HHS R01HL092020NIAID NIH HHS R01 AI103142NIAID NIH HHS R01AI103142
6 · The paper itself

Abstract

The cellular mechanisms controlling infection-induced emergency granulopoiesis are poorly defined. Here we found that reactive oxygen species (ROS) concentrations in the bone marrow (BM) were elevated during acute infection in a phagocytic NADPH oxidase-dependent manner in myeloid cells. Gr1(+) myeloid cells were uniformly distributed in the BM, and all c-kit(+) progenitor cells were adjacent to Gr1(+) myeloid cells. Inflammation-induced ROS production in the BM played a critical role in myeloid progenitor expansion during emergency granulopoiesis. ROS elicited oxidation and deactivation of phosphatase and tensin homolog (PTEN), resulting in upregulation of PtdIns(3,4,5)P3 signaling in BM myeloid progenitors. We further revealed that BM myeloid cell-produced ROS stimulated proliferation of myeloid progenitors via a paracrine mechanism. Taken together, our results establish that phagocytic NADPH oxidase-mediated ROS production by BM myeloid cells plays a critical role in mediating emergency granulopoiesis during acute infection.

Indexed as

HematopoiesisAcute DiseaseAnimalsBone MarrowCell ProliferationCells, CulturedEscherichia coliEscherichia coli InfectionsGranulocytesMiceMice, Inbred C57BLMice, TransgenicMyeloid CellsMyeloid Progenitor CellsNADPH OxidasesParacrine CommunicationNADPH Oxidasesphosphatidylinositol 3,4,5-triphosphatePhosphatidylinositol PhosphatesPTEN PhosphohydrolaseReactive Oxygen Species

Identifiers

PMID25579427
PMCPMC4303526
OpenAlexW1998668726

What OpenQuestion holds

Textmetadata
LicenceTDM
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.