Evidence map›Paper›PMID 29760725›Full record

ArticleStem cells international2018

The Effects of Hyperacute Serum on the Elements of the Human Subchondral Bone Marrow Niche.

Melinda Simon, Bálint Major, Gabriella Vácz, Olga Kuten, István Hornyák, Adél Hinsenkamp, Dorottya Kardos, Marcell Bagó, Domonkos Cseh, Adrienn Sárközi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Albumin as a Biomaterial and Therapeutic Agent in Regenerative Medicine.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Apolipoprotein A-I Supports MSCs Survival under Stress Conditions.International journal of molecular sciences · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

13 authors at 2 institutions in 2 countries.

Melinda SimonInstitute of Clinical Experimental Research, Semmelweis University, Budapest, Hungary.ORCID 0000-0001-9537-4248
Bálint MajorDepartment of Orthopedics, Polyclinic of the Hospitaller Brothers of St. John of God in Budapest, Budapest, Hungary.ORCID 0000-0002-0933-7908
Gabriella VáczInstitute of Clinical Experimental Research, Semmelweis University, Budapest, Hungary.
Olga KutenOrthosera GmbH, Krems an der Donau, Austria.ORCID 0000-0002-1827-1314
István HornyákInstitute of Clinical Experimental Research, Semmelweis University, Budapest, Hungary.
Adél HinsenkampInstitute of Clinical Experimental Research, Semmelweis University, Budapest, Hungary.
Dorottya KardosInstitute of Clinical Experimental Research, Semmelweis University, Budapest, Hungary.
Marcell BagóInstitute of Clinical Experimental Research, Semmelweis University, Budapest, Hungary.ORCID 0000-0003-0132-1044
Domonkos CsehDepartment of Physiology, Semmelweis University, Budapest, Hungary.ORCID 0000-0003-1955-5148
Adrienn SárköziDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Denes HorvathyInstitute of Clinical Experimental Research, Semmelweis University, Budapest, Hungary.ORCID 0000-0001-8136-7100
Stefan NehrerDanube University Krems, Krems an der Donau, Austria.
Zsombor LaczaInstitute of Clinical Experimental Research, Semmelweis University, Budapest, Hungary.
Semmelweis University · HUUniversität für Weiterbildung Krems · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are widely used in laboratory experiments as well as in human cell therapy. Their culture requires animal sera like fetal calf serum (FCS) as essential supplementation; however, animal sera pose a risk for clinical applications. Human blood derivatives, for example, platelet-rich plasma (PRP) releasates, are potential replacements of FCS; however, it is unclear which serum variant has the best effect on the given cell or tissue type. Additionally, blood derivatives are commonly used in musculoskeletal diseases like osteoarthritis (OA) or osteonecrosis as "proliferative agents" for the topical MSC pool. Hyperacute serum (HAS), a new serum derivative, has been designed to approximate the natural coagulation cascade with a single-step, additive-free preparation method. We investigated the effects of HAS on monolayer MSC cultures and in their natural niche, in 3D subchondral bone and marrow explants. Viability measurements, RT-qPCR evaluation for gene expression and flow cytometry for cell surface marker analysis were performed to compare the effects of FCS-, PRP-, or HAS-supplemented culture media. Monolayer MSCs showed significantly higher metabolic activity following 5 days' incubation in HAS, and osteoblast-specific mRNA expression was markedly increased, while cells also retained their MSC-specific cell surface markers. A similar effect was observed on bone and marrow explants, which was further confirmed with confocal microscopy analysis. Moreover, markedly higher bone marrow preservation was observed with histology in case of HAS supplementation compared to FCS. These findings indicate possible application of HAS in regenerative solutions of skeletal diseases like OA or osteonecrosis.

Identifiers

PMID29760725
PMCPMC5926480
OpenAlexW2800648016

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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.