Evidence map›Paper›PMID 34833250›Full record

ArticlePolymers2021

Culturing and Scaling up Stem Cells of Dental Pulp Origin Using Microcarriers.

Anna Földes, Hajnalka Reider, Anita Varga, Krisztina S Nagy, Katalin Perczel-Kovach, Katalin Kis-Petik, Pamela DenBesten, András Ballagi, Gábor Varga

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Research progress on optimization ofFrontiers in bioengineering and biotechnology · 2024
    Review
  5. Review
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 3 institutions in 2 countries.

Anna FöldesDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.
Hajnalka ReiderDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.
Anita VargaDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.
Krisztina S NagyDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.ORCID 0000-0002-4942-2947
Katalin Perczel-KovachDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.
Katalin Kis-PetikInstitute of Biophysics and Radiation Biology, Semmelweis University, H-1089 Budapest, Hungary.
Pamela DenBestenDepartment of Orofacial Science, University of California, San Francisco, CA 94143, USA.ORCID 0000-0002-2107-6229
András BallagiDepartment of Applied Biotechnology and Food Science, University of Technology and Economics, H-1089 Budapest, Hungary.
Gábor VargaDepartment of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.ORCID 0000-0002-5506-8198
Semmelweis University · HUGedeon Richter (Hungary) · HUUniversity of California, San Francisco · US

Funding

Enamel biomineralization; the role of pH cyclingR01DE027971 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Pamela K Den Besten · 2019 to 2026
$4.5M
ENAMEL FLUOROSIS;MECHANISMS OF ACTIONR01DE013508 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DEN BESTEN, PAMELA K · 2000 to 2013
$4.5M
Hungarian National Research, Development and Innovation Office NKFIH K-125161NIDCR NIH HHS 1R01DE027971NIDCR NIH HHS R01 DE013508NIDCR NIH HHS R01 DE027971
6 · The paper itself

Abstract

Ectomesenchymal stem cells derived from the dental pulp are of neural crest origin, and as such are promising sources for cell therapy and tissue engineering. For safe upscaling of these cells, microcarrier-based culturing under dynamic conditions is a promising technology. We tested the suitability of two microcarriers, non-porous Cytodex 1 and porous Cytopore 2, for culturing well characterized dental pulp stem cells (DPSCs) using a shake flask system. Human DPSCs were cultured on these microcarriers in 96-well plates, and further expanded in shake flasks for upscaling experiments. Cell viability was measured using the alamarBlue assay, while cell morphology was observed by conventional and two-photon microscopies. Glucose consumption of cells was detected by the glucose oxidase/Clark-electrode method. DPSCs adhered to and grew well on both microcarrier surfaces and were also found in the pores of the Cytopore 2. Cells grown in tissue culture plates (static, non-shaking conditions) yielded 7 × 10

Indexed as

Cytodex 1Cytopore 2dental pulpmesenchymalmicrocarrierscaffoldscaling upshake flaskstem cells

Identifiers

PMID34833250
PMCPMC8622966
OpenAlexW3213908348

What Socratic 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 Socratic graph.