Evidence map›Paper›PMID 41060335›Full record

ArticleBlood2026

Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche.

James W Swann, Ruiyuan Zhang, Evgenia V Verovskaya, Fernando J Calero-Nieto, Xiaonan Wang, Melissa A Proven, Hiroyuki Hirakawa, Brian P Heubel, Peter T Shyu, X Edward Guo and 3 more

Abstract read
In one paragraph

Article in Blood, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Neonatal critical illness is associated with pancytopenia development in childhood.medRxiv : the preprint server for health sciences · 2026
    Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

James W SwannDepartment of Genetics and Development, Columbia Stem Cell Initiative, Columbia University, New York, NY.ORCID 0000-0001-7988-9997
Ruiyuan ZhangDepartment of Genetics and Development, Columbia Stem Cell Initiative, Columbia University, New York, NY.ORCID 0000-0002-9530-0158
Evgenia V VerovskayaDepartment of Genetics and Development, Columbia Stem Cell Initiative, Columbia University, New York, NY.
Fernando J Calero-NietoCambridge Stem Cell Institute and Department of Haematology, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0003-3358-8253
Xiaonan WangCambridge Stem Cell Institute and Department of Haematology, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0003-3759-778X
Melissa A ProvenDepartment of Genetics and Development, Columbia Stem Cell Initiative, Columbia University, New York, NY.ORCID 0000-0001-6168-8644
Hiroyuki HirakawaDepartment of Rehabilitation and Regenerative Medicine, Columbia Stem Cell Initiative, Columbia University, New York, NY.
Brian P HeubelDepartment of Genetics and Development, Columbia Stem Cell Initiative, Columbia University, New York, NY.
Peter T ShyuDepartment of Biomedical Engineering, Columbia University, New York, NY.
X Edward GuoDepartment of Biomedical Engineering, Columbia University, New York, NY.ORCID 0000-0003-0804-7279
Lei DingDepartment of Rehabilitation and Regenerative Medicine, Columbia Stem Cell Initiative, Columbia University, New York, NY.
Berthold GöttgensCambridge Stem Cell Institute and Department of Haematology, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0001-6302-5705
Emmanuelle PasseguéDepartment of Genetics and Development, Columbia Stem Cell Initiative, Columbia University, New York, NY.ORCID 0000-0002-3516-297X

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Parisa Tehranifar · 1985 to 2026
$115.3M
Emergency Myelopoiesis Pathways in the Control of Blood ProductionR35HL135763 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PASSEGUE, EMMANUELLE · 2017 to 2023
$5.7M
New York Consortium for Interdisciplinary Training in Kidney, Urological and Hematological Research (NYC Train KUHR)TL1DK136048 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI JONATHAN M. BARASCH, Wadie F Bahou · 2022 to 2026
$3.8M
Emergency Myelopoiesis in the Control of Blood ProductionR35HL171521 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Emmanuelle Passegue · 2024 to 2026
$3.3M
Understanding the role of stellate cells in the liver hematopoietic stem cell nicheR01HL153487 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI DING, LEI · 2020 to 2024
$2.8M
Understanding and targeting bone marrow microenvironment in myelofibrosisR01HL155868 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI DING, LEI · 2021 to 2024
$2.3M
Developing Next Generation Genetics for Understanding Hematopoietic Stem Cell BiologyR01GM146061 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DING, LEI, YAZAWA, MASAYUKI · 2022 to 2025
$2.0M
Regulation of hematopoietic stem cells and leukemia stem cells by thrombopoietinR01HL132074 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI DING, LEI · 2016 to 2020
$2.0M
Role of autophagy in normal and transformed hematopoietic stem cellsR01CA184014 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PASSEGUE, EMMANUELLE · 2014 to 2018
$1.7M
NCI NIH HHS P30 CA013696NCI NIH HHS R01 CA184014NHLBI NIH HHS R01 HL132074NHLBI NIH HHS R01 HL153487NHLBI NIH HHS R01 HL155868NHLBI NIH HHS R35 HL135763NHLBI NIH HHS R35 HL171521NIDDK NIH HHS TL1 DK136048NIGMS NIH HHS R01 GM146061Wellcome Trust 206328
6 · The paper itself

Abstract

abstractHematopoietic stem and progenitor cells are regulated by interactions with stromal cells in the bone marrow (BM) cavity, which can be segregated into 2 spatially defined central marrow (CM) and endosteal (Endo) compartments. However, the importance of this spatial compartmentalization for BM responses to complex conditions such as inflammation remains largely unknown. Here, we extensively validate a combination of single-cell RNA sequencing profiling and matching flow cytometry isolation that reproducibly identifies 7 key CM and Endo populations and accurately surveys both niche locations. We demonstrate that inflammatory perturbations exert specific effects on different cellular compartments, with type I interferon responses causing leptin receptor-expressing mesenchymal stromal cells to abandon their normal stromal functions and instead adopt an inflammatory phenotype associated with overproduction of chemokines that modulate local monocyte dynamics in the surrounding microenvironment. Our results provide a comprehensive method for molecular and functional stromal characterization and highlight the importance of altered stomal cell activity in regulating hematopoietic responses to inflammatory challenges.

Indexed as

Bone MarrowBone Marrow CellsHematopoiesisInflammationStem Cell NicheAnimalsHematopoietic Stem CellsHumansMesenchymal Stem CellsMiceMice, Inbred C57BL

Identifiers

PMID41060335
PMCPMC7618457

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.