Evidence map›Paper›PMID 38277455›Full record

ArticleScience advances2024

Quantitative association between gene expression and blood cell production of individual hematopoietic stem cells in mice.

Du Jiang, Adnan Y Chowdhury, Anna Nogalska, Jorge Contreras, Yeachan Lee, Mary Vergel-Rodriguez, Melissa Valenzuela, Rong Lu

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.6field-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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. 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

8 authors at 1 institution in 1 country.

Du JiangDepartment of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.ORCID 0000-0003-2147-569X
Adnan Y ChowdhuryDepartment of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Anna NogalskaDepartment of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Jorge ContrerasDepartment of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Yeachan LeeDepartment of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Mary Vergel-RodriguezDepartment of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Melissa ValenzuelaDepartment of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.ORCID 0009-0007-8977-7682
Rong LuDepartment of Stem Cell Biology and Regenerative Medicine, Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.ORCID 0000-0002-5151-9246
University of Southern California · US

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fumito Ito · 1985 to 2026
$181.4M
Investigating the heterogeneity and coordination of hematopoietic stem cells (Diversity Supplement)R35HL150826 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Rong Lu · 2020 to 2026
$6.8M
Using spatial, single-cell genomic recording to investigate age-associated clonal hematopoiesisR01AG080982 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MICHAEL B ELOWITZ, CARLOS LOIS · 2023 to 2026
$2.1M
Tracing the developmental origin of hematopoietic stem cell heterogeneityR01HL138225 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LU, RONG · 2017 to 2019
$1.6M
Investigating the heterogeneous aging of individual hematopoietic stem cell clonesR01HL135292 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LU, RONG · 2017 to 2019
$1.5M
Lineage bias and clonal expansion of hematopoietic stem cell differentiationR00HL113104 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LU, RONG · 2014 to 2016
$747k
NCI NIH HHS P30 CA014089NHLBI NIH HHS R00 HL113104NHLBI NIH HHS R01 HL135292NHLBI NIH HHS R01 HL138225NHLBI NIH HHS R35 HL150826NIA NIH HHS R01 AG080982
6 · The paper itself

Abstract

Individual hematopoietic stem cells (HSCs) produce different amounts of blood cells upon transplantation. Taking advantage of the intercellular variation, we developed an experimental and bioinformatic approach to evaluating the quantitative association between gene expression and blood cell production across individual HSCs. We found that most genes associated with blood production exhibit the association only at some levels of blood production. By mapping gene expression with blood production, we identified four distinct patterns of their quantitative association. Some genes consistently correlate with blood production over a range of levels or across all levels, and these genes are found to regulate lymphoid but not myeloid production. Other genes exhibit one or more clear peaks of association. Genes with overlapping peaks are found to be coexpressed in other tissues and share similar molecular functions and regulatory motifs. By dissecting intercellular variations, our findings revealed four quantitative association patterns that reflect distinct dose-response molecular mechanisms modulating the blood cell production of HSCs.

Indexed as

Blood CellsHematopoietic Stem CellsAnimalsCell DifferentiationGene ExpressionMice

Identifiers

PMID38277455
PMCPMC10816716
OpenAlexW4391250348

What OpenQuestion 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 OpenQuestion graph.