Evidence map›Paper›PMID 32569325›Full record

ArticlePloS one2020

Biomimetic reconstruction of the hematopoietic stem cell niche for in vitro amplification of human hematopoietic stem cells.

L Marx-Blümel, C Marx, F Weise, J Frey, B Perner, G Schlingloff, N Lindig, J Hampl, J Sonnemann, D Brauer and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

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  5. MatriGridBioengineering (Basel, Switzerland) · 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

17 authors at 3 institutions in 1 country.

L Marx-BlümelDepartment of Paediatric Haematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.ORCID 0000-0002-9360-6559
C MarxLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany.
F WeiseInstitute for Micro and Nanotechnologies MacroNano®, Nano-Biosystem Technology, Ilmenau University of Technology, Ilmenau, Germany.
J FreyDepartment of Paediatric Haematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
B PernerLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany.
G SchlingloffInstitute for Micro and Nanotechnologies MacroNano®, Nano-Biosystem Technology, Ilmenau University of Technology, Ilmenau, Germany.
N LindigDepartment of Paediatric Haematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
J HamplInstitute for Micro and Nanotechnologies MacroNano®, Nano-Biosystem Technology, Ilmenau University of Technology, Ilmenau, Germany.
J SonnemannDepartment of Paediatric Haematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
D BrauerInstitute for Micro and Nanotechnologies MacroNano®, Nano-Biosystem Technology, Ilmenau University of Technology, Ilmenau, Germany.
A VoigtDepartment of Paediatric Haematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
S SinghInstitute for Micro and Nanotechnologies MacroNano®, Nano-Biosystem Technology, Ilmenau University of Technology, Ilmenau, Germany.
B BeckDepartment of Paediatric Haematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
Ute-Maria JägerDepartment of Paediatric Haematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
Z Q WangLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany.
J F BeckDepartment of Paediatric Haematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
A SchoberInstitute for Micro and Nanotechnologies MacroNano®, Nano-Biosystem Technology, Ilmenau University of Technology, Ilmenau, Germany.
Jena University Hospital · DETechnische Universität Ilmenau · DELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematopoietic stem cell transplantation is successfully applied since the late 1950s; however, its efficacy still needs to be increased. A promising strategy is to transplant high numbers of pluripotent hematopoietic stem cells (HSCs). Therefore, an improved ex vivo culture system that supports proliferation and maintains HSC pluripotency would override possible limitations in cell numbers gained from donors. To model the natural HSC niche in vitro, we optimized the HSC medium composition with a panel of cytokines and valproic acid and used an artificial 3D bone marrow-like scaffold made of polydimethylsiloxane (PDMS). This 3D scaffold offered a suitable platform to amplify human HSCs in vitro and, simultaneously, to support their viability, multipotency and ability for self-renewal. Silicon oxide-covering of PDMS structures further improved amplification of CD34+ cells, although the conservation of naïve HSCs was better on non-covered 3D PDMS. Finally, we found that HSC cultivated on non-covered 3D PDMS generated most pluripotent colonies within colony forming unit assays. In conclusion, by combining biological and biotechnological approaches, we optimized in vitro HSCs culture conditions, resulting in improved amplification, multipotency maintenance and vitality of HSCs.

Indexed as

Stem Cell NicheBiomimetic MaterialsCell ProliferationCells, CulturedCollagenDimethylpolysiloxanesFemaleFibronectinsHematopoietic Stem CellsHumansMalePurinesValproic AcidbaysilonCollagenDimethylpolysiloxanesFibronectinsPurinesStemRegenin 1Valproic Acid

Identifiers

PMID32569325
PMCPMC7307768
OpenAlexW3036527257

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.