Evidence map›Paper›PMID 33357408›Full record

ArticleStem cell reports2021

Chicken Interspecies Chimerism Unveils Human Pluripotency.

Azimeh Akhlaghpour, Adeleh Taei, Seyyed Abolghasem Ghadami, Zahra Bahadori, Saeed Yakhkeshi, Sepideh Molamohammadi, Tahereh Kiani, Azam Samadian, Zahra Ghezelayagh, Newsha Haghparast and 4 more

Abstract read
In one paragraph

Article in Stem cell reports, 2021. 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
–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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. International journal of stem cells · 2022
    Review
  6. Avian Embryonic Culture: A Perspective ofFrontiers in physiology · 2022
    Review
  7. 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

14 authors.

Azimeh AkhlaghpourDepartment of Developmental Biology, University of Science and Culture, Tehran, Iran; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran.
Adeleh TaeiDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran.
Seyyed Abolghasem GhadamiDepartment of Biotechnology, Faculty of Biological Sciences, Alzahra University, Tehran, Iran.
Zahra BahadoriDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran.
Saeed YakhkeshiDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran.
Sepideh MolamohammadiDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran.
Tahereh KianiDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran.
Azam SamadianDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran.
Zahra GhezelayaghDepartment of Developmental Biology, University of Science and Culture, Tehran, Iran; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran.
Newsha HaghparastDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran.
Keynoosh KhalooghiDepartment of Cardiac Development and Remodeling, Max-Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.
Thomas BraunDepartment of Cardiac Development and Remodeling, Max-Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.
Hossein BaharvandDepartment of Developmental Biology, University of Science and Culture, Tehran, Iran; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran. Electronic address: baharvand@royaninstitute.org.
Seyedeh-Nafiseh HassaniDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Banihashem Sq., Banihashem St., Resalat Highway, Tehran, Iran. Electronic address: snafiseh.hassani@royaninstitute.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human pluripotent stem cells (hPSCs) are commonly kept in a primed state but also able to acquire a more immature naive state under specific conditions in vitro. Acquisition of naive state changes several properties of hPSCs and might affect their contribution to embryonic development in vivo. However, the lack of an appropriate animal test system has made it difficult to assess potential differences for chimera formation between naive and primed hPSCs. Here, we report that the developing chicken embryo is a permissive host for hPSCs, allowing analysis of the pluripotency potential of hPSCs. Transplantation of naive-like and primed hPSCs at matched developmental stages resulted in robust chimerism. Importantly, the ability of naive-like but not of primed hPSCs to form chimera was substantially reduced when injected at non-matched developmental stages. We propose that contribution to chick embryogenesis is an informative and versatile test to identify different pluripotent states of hPSCs.

Indexed as

AnimalsCell DifferentiationCell LineageChick EmbryoChickensChimerismEmbryonic DevelopmentGene EditingHumansLIM-Homeodomain ProteinsPluripotent Stem CellsSOXB1 Transcription FactorsTranscription FactorsTubulininsulin gene enhancer binding protein Isl-1LIM-Homeodomain ProteinsSOXB1 Transcription FactorsTranscription FactorsTubulinchick embryochimera formationinterspecies chimera formationnaive and primed human pluripotent statespluripotency

Identifiers

PMID33357408
PMCPMC7815937

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.