Evidence map›Paper›PMID 36542833›Full record

ArticleBlood2023

The tetraspanin CD53 protects stressed hematopoietic stem cells via promotion of DREAM complex-mediated quiescence.

Zev J Greenberg, Luana Chiquetto Paracatu, Darlene A Monlish, Qian Dong, Michael Rettig, Nate Roundy, Rofaida Gaballa, Weikai Li, Wei Yang, Cliff J Luke and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Blood, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  5. HSPCs and TScience advances · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Zev J GreenbergDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-6234-7005
Luana Chiquetto ParacatuDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO.
Darlene A MonlishDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0003-3374-9117
Qian DongDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO.
Michael RettigDepartment of Oncology, Washington University School of Medicine, St. Louis, MO.
Nate RoundyDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO.
Rofaida GaballaDepartment of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO.
Weikai LiDepartment of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-8711-1904
Wei YangDepartment of Genetics, Washington University School of Medicine, St. Louis, MO.
Cliff J LukeDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-7408-2374
Laura G SchuettpelzDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-6047-3641
Washington University in St. Louis · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
TRAINING PROGRAM IN CELLULAR AND MOLECULAR BIOLOGYT32GM007067 · NIGMS · WASHINGTON UNIVERSITY · PI TRUE-KROB, HEATHER L · 1985 to 2020
$20.4M
ROLE OF TLR2 IN REGULATING NORMAL AND PREMALIGNANT HEMATOPOIETIC STEM CELLSR01HL134896 · NHLBI · WASHINGTON UNIVERSITY · PI LAURA G. SCHUETTPELZ · 2017 to 2026
$3.5M
Inhibitors of Intestinal Epithelial Cell Lysosomal-Mediated NecrosisR01DK114047 · NIDDK · WASHINGTON UNIVERSITY · PI LUKE, CLIFFORD JAMES, SILVERMAN, GARY ARTHUR · 2018 to 2021
$1.7M
NCI NIH HHS P30 CA091842NHLBI NIH HHS R01 HL134896NIDDK NIH HHS R01 DK114047NIGMS NIH HHS T32 GM007067
6 · The paper itself

Abstract

The hematopoietic stem cell (HSC) cycle responds to inflammatory and other proliferative stressors; however, these cells must quickly return to quiescence to avoid exhaustion and maintain their functional integrity. The mechanisms that regulate this return to quiescence are not well understood. Here, we show that tetraspanin CD53 is markedly upregulated in HSCs in response to a variety of inflammatory and proliferative stimuli and that the loss of CD53 is associated with prolonged cycling and reduced HSC function in the context of inflammatory stress. Mechanistically, CD53 promotes the activity of the dimerization partner, RB-like, E2F, and multi-vulva class B (DREAM) transcriptional repressor complex, which downregulates genes associated with cycling and division. Proximity labeling and confocal fluorescence microscopy studies showed that CD53 interacts with DREAM-associated proteins, specifically promoting the interaction between Rbl2/p130 and its phosphatase protein phosphatase 2A (PP2A), effectively stabilizing p130 protein availability for DREAM binding. Together, these data identified a novel mechanism by which stressed HSCs resist cycling.

Indexed as

Hematopoietic Stem CellsTetraspanin 25AnimalsCell DivisionFemaleHumansMiceCd53 protein, mouseTetraspanin 25

Identifiers

PMID36542833
PMCPMC10023726
OpenAlexW4312093914

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.