Evidence map›Paper›PMID 27341538›Full record

ArticleJournal of visualized experiments : JoVE2016

Generation of Parabiotic Zebrafish Embryos by Surgical Fusion of Developing Blastulae.

Elliott J Hagedorn, Jennifer L Cillis, Caitlyn R Curley, Taylor C Patch, Brian Li, Bradley W Blaser, Raquel Riquelme, Leonard I Zon, Dhvanit I Shah

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Wdr5-mediated H3K4 methylation facilitates HSPC development via maintenance of genomic stability in zebrafish.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

9 authors at 5 institutions in 1 country.

Elliott J HagedornDivision of Hematology/Oncology, Boston Children's Hospital; Harvard Medical School.
Jennifer L CillisDivision of Hematology, Department of Medicine, Brigham and Women's Hospital.
Caitlyn R CurleyDivision of Hematology, Department of Medicine, Brigham and Women's Hospital.
Taylor C PatchDivision of Hematology, Department of Medicine, Brigham and Women's Hospital.
Brian LiDivision of Hematology/Oncology, Boston Children's Hospital; Harvard Medical School.
Bradley W BlaserDivision of Hematology/Oncology, Boston Children's Hospital; Harvard Medical School; Division of Hematologic Malignancies, Dana-Farber Cancer Institute.
Raquel RiquelmeDivision of Hematology/Oncology, Boston Children's Hospital; Harvard Medical School.
Leonard I ZonDivision of Hematology/Oncology, Boston Children's Hospital; Harvard Medical School; Harvard Stem Cell Institute; Broad Institute of Massachusetts Institute of Technology; Howard Hughes Medical Institute.
Dhvanit I ShahDivision of Hematology/Oncology, Boston Children's Hospital; Harvard Medical School; Division of Hematology, Department of Medicine, Brigham and Women's Hospital; Harvard Stem Cell Institute; Broad Institute of Massachusetts Institute of Technology; DSHAH@research.bwh.harvard.edu.
Brigham and Women's Hospital · USBoston Children's Hospital · USHarvard University · USBroad Institute · USMassachusetts Institute of Technology · US

Funding

TRANSCRIPTION FACTOR GATA-1 IN TERMINAL ERYTHROID DEVELOPMENTP01HL032262 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI ZON, LEONARD IRA · 1985 to 2021
$38.9M
Customized stem cells for clinical application in blood disordersR24DK092760 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI COLLINS, JAMES J, DALEY, GEORGE Q · 2011 to 2018
$10.7M
TRANSFUSION BIOLOGY AND MEDICINET32HL066987 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI JOHN P MANIS · 2001 to 2026
$10.2M
Cancer Biology in the ZebrafishR01CA103846 · NCI · CHILDREN'S HOSPITAL BOSTON · PI ZON, LEONARD IRA · 2003 to 2022
$7.5M
Project-002U54DK110805 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI ORKIN, STUART H, ZON, LEONARD IRA · 2016 to 2020
$5.9M
EMBRYONIC HEMATOPOIESISR01HL048801 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI ZON, LEONARD IRA · 1992 to 2016
$5.7M
Biomechanical Stimulation of Hemogenic Endothelial Cells to Develop Clinical-Grade Hematopoietic Stem CellsR01HL131645 · NHLBI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI SHAH, DHVANIT INDRAVADAN · 2016 to 2019
$1.6M
Zebrafish Genetics to Identify Genes Involved in HematopoiesisK01DK085217 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI SHAH, DHVANIT INDRAVADAN · 2010 to 2014
$794k
Analysis of Mammalian Hematological Diseases in a Mouse Atpif1 Deficient ModelsR03DK100672 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI SHAH, DHVANIT INDRAVADAN · 2014 to 2015
$177k
Howard Hughes Medical InstituteNCI NIH HHS R01 CA103846NHLBI NIH HHS P01 HL032262NHLBI NIH HHS R01 HL048801NHLBI NIH HHS R01 HL131645NHLBI NIH HHS T32 HL066987NIDDK NIH HHS K01 DK085217NIDDK NIH HHS R03 DK100672NIDDK NIH HHS R24 DK092760NIDDK NIH HHS U54 DK110805
6 · The paper itself

Abstract

Surgical parabiosis of two animals of different genetic backgrounds creates a unique scenario to study cell-intrinsic versus cell-extrinsic roles for candidate genes of interest, migratory behaviors of cells, and secreted signals in distinct genetic settings. Because parabiotic animals share a common circulation, any blood or blood-borne factor from one animal will be exchanged with its partner and vice versa. Thus, cells and molecular factors derived from one genetic background can be studied in the context of a second genetic background. Parabiosis of adult mice has been  used extensively to research aging, cancer, diabetes, obesity, and brain development. More recently, parabiosis of zebrafish embryos has been used to study the developmental biology of hematopoiesis. In contrast to mice, the transparent nature of zebrafish embryos permits the direct visualization of cells in the parabiotic context, making it a uniquely powerful method for investigating fundamental cellular and molecular mechanisms. The utility of this technique, however, is limited by a steep learning curve for generating the parabiotic zebrafish embryos. This protocol provides a step-by-step method on how to surgically fuse the blastulae of two zebrafish embryos of different genetic backgrounds to investigate the role of candidate genes of interest. In addition, the parabiotic zebrafish embryos are tolerant to heat shock, making temporal control of gene expression possible. This method does not require a sophisticated set-up and has broad applications for studying cell migration, fate specification, and differentiation in vivo during embryonic development.

Indexed as

BlastulaAnimalsCell MovementHematopoiesisMiceParabiosisZebrafish

Identifiers

PMID27341538
PMCPMC4927786
OpenAlexW2414398519

What OpenQuestion holds

Textmetadata
LicenceTDM
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.