Evidence map›Paper›PMID 29577749›Full record

ArticleCartilage2020

Proliferation, Migration, and ECM Formation Potential of Human Annulus Fibrosus Cells Is Independent of Degeneration Status.

Sylvia Hondke, Mario Cabraja, Jan Philipp Krüger, Stefan Stich, Tony Hartwig, Michael Sittinger, Michaela Endres

Open access · bronzeAbstract read
In one paragraph

Article in Cartilage, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.2field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Orthobiologic Management Options for Degenerative Disc Disease.Bioengineering (Basel, Switzerland) · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Effect of Platelet-Rich Plasma on Intervertebral Disc DegenerationOxidative medicine and cellular longevity · 2020
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. 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

7 authors at 4 institutions in 1 country.

Sylvia HondkeTransTissue Technologies GmbH, Berlin, Germany.ORCID 0000-0001-7742-5128
Mario CabrajaDepartment of Spinal Surgery, Vivantes Auguste-Viktoria-Hospital, Berlin, Germany.
Jan Philipp KrügerTransTissue Technologies GmbH, Berlin, Germany.
Stefan StichDepartment of Rheumatology and Clinical Immunology, Tissue Engineering Laboratory, Berlin-Brandenburg Center for Regenerative Therapies and Department of Rheumatology and Clinical Immunology, Berlin, Germany.
Tony HartwigDepartment of Spinal Surgery, Vivantes Hospital Spandau, Berlin, Germany.
Michael SittingerDepartment of Rheumatology and Clinical Immunology, Tissue Engineering Laboratory, Berlin-Brandenburg Center for Regenerative Therapies and Department of Rheumatology and Clinical Immunology, Berlin, Germany.
Michaela EndresTransTissue Technologies GmbH, Berlin, Germany.
TransTissue (Germany) · DEBerlin-Brandenburger Centrum für Regenerative Therapien · DEAuguste-Viktoria-Klinik · DEVivantes Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe objective was to evaluate the proliferating, migratory and extracellular matrix (ECM) forming potential of annulus fibrosus cells derived from early (edAFC) or advanced (adAFC) degenerative tissue and their usability as a possible cell source for regenerative approaches for AF closure.

designEdAFC (

resultsEdAFC and adAFC were significantly attracted by 10% HS and 5% PRP. Additionally, both cell groups proliferated under stimulation with HS. Stimulation with 10 ng/mL TGFB3 showed significant induction of gene expression of collagen type II and aggrecan, while 5% PRP decreased the expression of collagen type I. Both cell groups showed formation of AF-like ECM after stimulation with TGFB3, whereas stimulation with PRP did not.

conclusionsOur study demonstrated that AF cells retain their potential for proliferation, migration, and ECM formation independent of the degeneration status of the tissue. Proliferation, migration, and ECM synthesis of the endogenous AF cells can be supported by different supplements. Hence, endogenous AF cells might be a suitable cell source for a regenerative repair approaches.

Indexed as

Annulus FibrosusCell MovementCell ProliferationCells, CulturedExtracellular MatrixHumansIntervertebral DiscIntervertebral Disc DegenerationPlatelet-Rich PlasmaRegenerationSerumTransforming Growth Factor beta3TGFB3 protein, humanTransforming Growth Factor beta3biomaterialsintervertebral disc cartilageplatelet-rich plasmapolymersrepairtissuetissue engineering

Identifiers

PMID29577749
PMCPMC7097975
OpenAlexW2789243921

What OpenQuestion holds

Textmetadata
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.