Evidence map›Paper›PMID 31408003›Full record

ArticleeLife2019

B cells suppress medullary granulopoiesis by an extracellular glycosylation-dependent mechanism.

Eric E Irons, Melissa M Lee-Sundlov, Yuqi Zhu, Sriram Neelamegham, Karin M Hoffmeister, Joseph Ty Lau

Open 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. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  4. Review
  5. CCR3-dependent eosinophil recruitment is regulated by sialyltransferase ST3Gal-IV.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  15. Global view of human protein glycosylation pathways and functions.Nature reviews. Molecular cell biology · 2020
    Review
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  18. Article
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

6 authors at 3 institutions in 1 country.

Eric E IronsDepartment of Molecular and Cellular Biology, Roswell Park Comprehensive Cancer Center, Buffalo, United States.
Melissa M Lee-SundlovBlood Research Institute Versiti, Milwaukee, United States.ORCID 0000-0002-8290-8586
Yuqi ZhuDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, United States.
Sriram NeelameghamDepartment of Chemical and Biological Engineering, University at Buffalo, Buffalo, United States.
Karin M HoffmeisterBlood Research Institute Versiti, Milwaukee, United States.
Joseph Ty LauDepartment of Molecular and Cellular Biology, Roswell Park Comprehensive Cancer Center, Buffalo, United States.ORCID 0000-0002-5128-2664
Roswell Park Comprehensive Cancer Center · USUniversity at Buffalo, State University of New York · USVersiti Blood Center of Wisconsin · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Dean G. Tang · 1985 to 2026
$116.6M
Carbohydrate-Mediated Platelet ClearanceR01HL089224 · NHLBI · VERSITI WISCONSIN, INC. · PI Karin Maria Hoffmeister · 2007 to 2026
$9.3M
Systems Biology of GlycosylationR01HL103411 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI NEELAMEGHAM, SRIRAM · 2011 to 2025
$7.1M
Glycans in Blood Homeostasis and DiseaseK12HL141954 · NHLBI · VERSITI WISCONSIN, INC. · PI DAHMS, NANCY M., DESAI, UMESH RAMANLAL · 2018 to 2022
$4.9M
ST6Gal-1 Sialyltransferase in InflammationR01AI140736 · NIAID · ROSWELL PARK CANCER INSTITUTE CORP · PI LAU, JOSEPH TY · 2018 to 2021
$3.9M
NCI NIH HHS CA076056NCI NIH HHS P30 CA016056NHLBI NIH HHS K12 HL141954NHLBI NIH HHS R01 HL089224NHLBI NIH HHS R01 HL103411NIAID NIH HHS R01 AI140736NIH HHS K12HK141954NIH HHS K12HL141954NIH HHS R01AI140736NIH HHS R01HL089224
6 · The paper itself

Abstract

The immune response relies on the integration of cell-intrinsic processes with cell-extrinsic cues. During infection, B cells vacate the marrow during emergency granulopoiesis but return upon restoration of homeostasis. Here we report a novel glycosylation-mediated crosstalk between marrow B cells and hematopoietic progenitors. Human B cells secrete active ST6GAL1 sialyltransferase that remodels progenitor cell surface glycans to suppress granulopoiesis. In mouse models, ST6GAL1 from B cells alters the sialylation profile of bone marrow populations, and mature IgD+ B cells were enriched in sialylated bone marrow niches. In clinical multiple myeloma, ST6GAL1 abundance in the multiple myeloma cells negatively correlated with neutrophil abundance. These observations highlight not only the ability of medullary B cells to influence blood cell production, but also the disruption to normal granulopoiesis by excessive ST6GAL1 in malignancy.

Indexed as

Cell CommunicationAnimalsbeta-D-Galactoside alpha 2-6-SialyltransferaseB-LymphocytesCell DifferentiationCells, CulturedCoculture TechniquesGlycosylationGranulocytesHumansMice, Inbred C57BLMice, KnockoutSialyltransferasesbeta-D-Galactoside alpha 2-6-SialyltransferaseSialyltransferasesB cellsglycosylationgranulopoiesishematopoietichumanimmunologyinflammationmousesialyltransferase

Identifiers

PMID31408003
PMCPMC6713473
OpenAlexW2967415845

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.