Evidence map›Paper›PMID 24673111›Full record

ArticleBritish journal of haematology2014

Temporal definition of haematopoietic stem cell niches in a large animal model of in utero stem cell transplantation.

Christine Jeanblanc, Angelina Daisy Goodrich, Evan Colletti, Saloomeh Mokhtari, Christopher D Porada, Esmail D Zanjani, Graça Almeida-Porada

Open access · bronzeAbstract read
In one paragraph

Article in British journal of haematology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. The making of cells and organs in xenogeneic animal bioreactor.Signal transduction and targeted therapy · 2026
    Review
  2. Article
  3. Review
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  6. Frontiers in cell and developmental biology · 2020
    Review
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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

7 authors at 3 institutions in 1 country.

Christine JeanblancDepartment of Agriculture, Nutrition and Veterinary Sciences, University of Nevada, Reno, NV, USA.
Angelina Daisy Goodrich
Evan Colletti
Saloomeh Mokhtari
Christopher D Porada
Esmail D Zanjani
Graça Almeida-Porada
University of Nevada, Reno · USForest Institute · USWake Forest University · US

Funding

IN UTERO STEM CELL TRANSPLANTATIONR01HL052955 · NHLBI · UNIVERSITY OF NEVADA RENO · PI ZANJANI, ESMAIL · 1994 to 2011
$4.6M
Functional Analysis of the Hematopoietic Niche during OntogenyR01HL097623 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ALMEIDA-PORADA, GRACA DUARTE · 2009 to 2012
$1.4M
NHLBI NIH HHS HL52955NHLBI NIH HHS R01 HL052955NHLBI NIH HHS R01 HL097623NHLBI NIH HHS R01HL097623
6 · The paper itself

Abstract

The fetal sheep model has served as a biologically relevant and translational model to study in utero haematopoietic stem cell transplantation (IUHSCT), yet little is known about the ontogeny of the bone marrow (BM) niches in this model. Because the BMmicroenvironment plays a critical role in the outcome of haematopoietic engraftment, we have established the correlation between the fetal-sheep and fetal-human BM niche ontogeny, so that studies addressing the role of niche development at the time of IUHSCT could be accurately performed. Immunofluorescence confocal microscopic analysis of sheep fetal bone from gestational days (gd) 25-68 showed that the BM microenvironment commences development with formation of the vascular niche between 25 and 36 gd in sheep; correlating with the events at 10-11 gestational weeks (gw) in humans. Subsequently, between 45 and 51 gd in sheep (c. 14 gw in humans), the osteoblastic/endosteal niche started developing, the presence of CD34(+)  CD45(+) cells were promptly detected, and their number increased with gestational age. IUHSCT, performed in sheep at 45 and 65 gd, showed significant haematopoietic engraftment only at the later time point, indicating that a fully functional BM microenvironment improved engraftment. These studies show that sheep niche ontogeny closely parallels human, validating this model for investigating niche influence/manipulation in IUHSCT engraftment.

Indexed as

Hematopoietic Stem Cell TransplantationModels, AnimalAnimalsAntigens, CD34Bone MarrowBone Marrow CellsFemaleFetal DevelopmentFetusGestational AgeGraft SurvivalHeterograftsHumansOsteoblastsPregnancySheepAntigens, CD34haematopoietic nichein uteroosteoblasttransplantationvascular

Identifiers

PMID24673111
PMCPMC4079736
OpenAlexW2023301014

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.