Evidence map›Paper›PMID 33351115›Full record

ArticleBlood advances2020

A novel conditioning-free hematopoietic stem cell transplantation model in zebrafish.

Ellen Fraint, María Feliz Norberto, Teresa V Bowman

Abstract read
In one paragraph

Article in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

3 authors.

Ellen FraintDepartment of Pediatrics (Hematology/Oncology), Children's Hospital at Montefiore, Bronx, NY.
María Feliz NorbertoNational Institutes of Health Postbaccalaureate Research Education Program, Albert Einstein College of Medicine, Bronx, NY; and.
Teresa V BowmanGottesman Institute for Stem Cell Biology and Regenerative Medicine, Department of Developmental and Molecular Biology and Department of Medicine (Oncology), Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY.

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI STEVEN C. ALMO · 1985 to 2026
$111.2M
Einstein Postbaccalaureate Research Education ProgramR25GM104547 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI AKABAS, MYLES H. · 2013 to 2023
$4.0M
Crosstalk of Splicing and Signaling in HSPC fate choicesR01DK121738 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BOWMAN, TERESA V · 2020 to 2023
$1.6M
Identification of novel regulators of HSC specification and maturationR01DK131445 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BOWMAN, TERESA V · 2021 to 2023
$868k
Crosstalk of Splicing and Signaling during HSC FormationR56DK121738 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BOWMAN, TERESA V · 2019 to 2019
$100k
NCI NIH HHS P30 CA013330NHLBI NIH HHS L40 HL165500NIDDK NIH HHS R01 DK121738NIDDK NIH HHS R01 DK131445NIDDK NIH HHS R56 DK121738NIGMS NIH HHS R25 GM104547
6 · The paper itself

Abstract

Transplantation is the most common assay for measuring the in vivo functionality of hematopoietic stem cells (HSCs). Although various HSC transplantation strategies have been developed in zebrafish, they are underutilized because of challenges related to immune matching and preconditioning toxicity. To circumvent these limitations, we developed a simple and robust transplantation model using HSC-deficient hosts. Homozygous runx1W84X mutants are devoid of definitive hematopoietic cells, including HSCs and adaptive immune cells; thus, they require no preconditioning regimen for transplantation. Marrow cell transplantation into runx1-mutant zebrafish 2 days after fertilization significantly improved their survival to adulthood and resulted in robust, multilineage, long-lasting, serially repopulating engraftment. Furthermore, we demonstrated that engraftment into runx1 homozygous mutants was significantly higher than into runx1 heterozygotes, demonstrating that the improved transplantation success is attributable to the empty HSC niche in mutants and not just the embryonic environment. Competitive transplantation of marrow cells into runx1 mutants revealed a stem cell frequency similar to that of murine marrow cells, which demonstrates the utility of this model for quantifying HSC function. The streamlined approach and robustness of this assay will help broaden its feasibility for future high-throughput transplantation experiments in zebrafish and will enable further novel discoveries in the biology of HSCs.

Indexed as

Hematopoietic Stem Cell TransplantationZebrafishAnimalsBone MarrowBone Marrow TransplantationHematopoietic Stem CellsMice

Identifiers

PMID33351115
PMCPMC7756993

What OpenQuestion holds

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Registered trials

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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.