Evidence map›Paper›PMID 34206516›Full record

ArticleCells2021

Bone Marrow-Derived VSELs Engraft as Lung Epithelial Progenitor Cells after Bleomycin-Induced Lung Injury.

Andrzej K Ciechanowicz, Katarzyna Sielatycka, Monika Cymer, Marta Skoda, Malwina Suszyńska, Kamila Bujko, Mariusz Z Ratajczak, Diane S Krause, Magdalena Kucia

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-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

15 citing papers in PubMed, 19 citations in OpenAlex.

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  12. Industrialized GMP Production of CD34Stem cell reviews and reports · 2022
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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 4 institutions in 2 countries.

Andrzej K CiechanowiczDepartment of Regenerative Medicine, Center for Preclinical Research and Technology, Medical University of Warsaw, 02-097 Warsaw, Poland.ORCID 0000-0003-0052-136X
Katarzyna SielatyckaInstitute of Biology, Faculty of Exact and Natural Sciences, University of Szczecin, 71-415 Szczecin, Poland.ORCID 0000-0003-4272-2266
Monika CymerDepartment of Regenerative Medicine, Center for Preclinical Research and Technology, Medical University of Warsaw, 02-097 Warsaw, Poland.
Marta SkodaDepartment of Regenerative Medicine, Center for Preclinical Research and Technology, Medical University of Warsaw, 02-097 Warsaw, Poland.
Malwina SuszyńskaStem Cell Institute at James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Kamila BujkoStem Cell Institute at James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.ORCID 0000-0002-2205-1154
Mariusz Z RatajczakDepartment of Regenerative Medicine, Center for Preclinical Research and Technology, Medical University of Warsaw, 02-097 Warsaw, Poland.
Diane S KrauseDepartments of Laboratory Medicine, Cell Biology and Pathology and the Yale Stem Cell Center, Yale University School of Medicine, New Haven, CT 06509, USA.
Magdalena KuciaDepartment of Regenerative Medicine, Center for Preclinical Research and Technology, Medical University of Warsaw, 02-097 Warsaw, Poland.
University of Louisville · USMedical University of Warsaw · PLUniversity of Szczecin · PLYale Cancer Center · US

Funding

Type II pneumocyte engraftment of bone marrow stem cellsR01HL073742 · NHLBI · YALE UNIVERSITY · PI KRAUSE, DIANE S · 2003 to 2012
$3.5M
National Science Center 2017/01/X/NZ3/00250National Science Center UMO-2014/14/M/NZ3/00475NHLBI NIH HHS R01 HL073742
6 · The paper itself

Abstract

backgroundAlveolar type 2 (AT2) cells and bronchioalveolar stem cells (BASC) perform critical regenerative functions in response to lung damage. Published data show that nonhematopoietic, bone marrow-derived "very small embryonic-like stem cells" (VSELs) can differentiate in vivo into surfactant protein C (SPC)-producing AT2 cells in the lung. Here, we test directly whether VSEL-derived BASC and AT2 cells function to produce differentiated progeny.

methodsusing a reporter mouse in which the H2B-GFP fusion protein is driven from the murine SPC promoter, we tested whether bone marrow-derived VSELs or non-VSEL/nonhematopoietic stem cells (non-VSEL/non-HSCs) can differentiate into AT2 and BASC cells that function as progenitor cells. Immediately following bleomycin administration, WT recipient mice underwent intravenous administration of VSELs or non-VSEL/non-HSCs from SPC H2B-GFP mice. GFP+ AT2 and BASC were isolated and tested for progenitor activity using in vitro organoid assays.

resultsafter 21 days in vivo, we observed differentiation of VSELs but not non-VSEL/non-HSCs into phenotypic AT2 and BASC consistent with previous data in irradiated recipients. Subsequent in vitro organoid assays revealed that VSEL-derived AT2 and BASC maintained physiological potential for differentiation and self-renewal.

conclusionthese findings prove that VSELs produce functional BASC and AT2 cells, and this may open new avenues using VSELs to develop effective cell therapy approaches for patients with lung injury.

Indexed as

Alveolar Epithelial CellsAnimalsBleomycinBone Marrow CellsEmbryonic Stem CellsEpithelial CellsGreen Fluorescent ProteinsHematopoietic Stem CellsLung InjuryMiceMice, Inbred C57BLOrganoidsRNA, MessengerBleomycinGreen Fluorescent ProteinsRNA, Messengeralveolar type II cellsbleomycin-induced injurybronchioalveolar stem cellslung regenerationregenerative medicinevery small embryonic-like stem cells

Identifiers

PMID34206516
PMCPMC8303224
OpenAlexW3174233669

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.