Evidence map›Paper›PMID 34486211›Full record

ArticleJournal of cellular and molecular medicine2021

Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture.

Nina Seidelmann, Daniela F Duarte Campos, Malena Rohde, Sandra Johnen, Sabine Salla, Gary Hin-Fai Yam, Jodhbir S Mehta, Peter Walter, Matthias Fuest

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 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
1.5field-weighted citation impact, top 17% 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, 17 citations in OpenAlex.

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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 3 countries.

Nina SeidelmannDepartment of Ophthalmology, RWTH Aachen University, Aachen, Germany.
Daniela F Duarte CamposInstitute of Applied Medical Engineering, RWTH Aachen University Hospital, Aachen, Germany.
Malena RohdeDepartment of Ophthalmology, RWTH Aachen University, Aachen, Germany.
Sandra JohnenDepartment of Ophthalmology, RWTH Aachen University, Aachen, Germany.
Sabine SallaDepartment of Ophthalmology, RWTH Aachen University, Aachen, Germany.
Gary Hin-Fai YamDepartment of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-8445-3669
Jodhbir S MehtaTissue Engineering and Cell Therapy Group, Singapore Eye Research Institute, Singapore, Singapore.
Peter WalterDepartment of Ophthalmology, RWTH Aachen University, Aachen, Germany.
Matthias FuestDepartment of Ophthalmology, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-0573-2599
RWTH Aachen University · DEHeidelberg University · DENational University of Singapore · SGUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The isolation and propagation of primary human corneal stromal keratocytes (CSK) are crucial for cellular research and corneal tissue engineering. However, this delicate cell type easily transforms into stromal fibroblasts (SF) and scar inducing myofibroblasts (Myo-SF). Current protocols mainly rely on xenogeneic fetal bovine serum (FBS). Human platelet lysate (hPL) could be a viable, potentially autologous, alternative. We found high cell survival with both supplements in CSK and SF. Cell numbers and Ki67+ ratios increased with higher fractions of hPL and FBS in CSK and SF. We detected a loss in CSK marker expression (Col8A2, ALDH3A1 and LUM) with increasing fractions of FBS and hPL in CSK and SF. The expression of the Myo-SF marker SMA increased with higher amounts of FBS but decreased with incremental hPL substitution in both cell types, implying an antifibrotic effect of hPL. Immunohistochemistry confirmed the RT-PCR findings. bFGF and HGF were only found in hPL and could be responsible for suppressing the Myo-SF conversion. Considering all findings, we propose 0.5% hPL as a suitable substitution in CSK culture, as this xeno-free component efficiently preserved CSK characteristics, with non-inferiority in terms of cell viability, cell number and proliferation in comparison to the established 0.5% FBS protocol.

Indexed as

Cell Culture TechniquesCulture MediaSerum Albumin, BovineAgedAnimalsBiomarkersBlood PlateletsCattleCell SurvivalCorneal KeratocytesCorneal StromaFemaleFibroblastsHumansImmunohistochemistryMaleBiomarkersCulture MediaSerum Albumin, Bovinecell culturecorneakeratocyte

Identifiers

PMID34486211
PMCPMC8505853
OpenAlexW3197568453

What OpenQuestion holds

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LicenceCC BY
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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.