Evidence map›Paper›PMID 38337220›Full record

ArticlePolymers2024

The Phenotype of Mesenchymal Stromal Cell and Articular Chondrocyte Cocultures on Highly Porous Bilayer Poly-L-Lactic Acid Scaffolds Produced by Thermally Induced Phase Separation and Supplemented with Hydroxyapatite.

Wally Ferraro, Aurelio Civilleri, Clemens Gögele, Camilla Carbone, Ilenia Vitrano, Francesco Carfi Pavia, Valerio Brucato, Vincenzo La Carrubba, Christian Werner, Kerstin Schäfer-Eckart and 1 more

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

11 authors at 3 institutions in 2 countries.

Wally FerraroEngineering Department, Università degli Studi di Palermo, V.le delle Scienze Building 6, 90128 Palermo, Italy.
Aurelio CivilleriEngineering Department, Università degli Studi di Palermo, V.le delle Scienze Building 6, 90128 Palermo, Italy.
Clemens GögeleInstitute of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, Prof. Ernst Nathan Str. 1, 90419 Nuremberg, Germany.ORCID 0000-0002-7086-9743
Camilla CarboneEngineering Department, Università degli Studi di Palermo, V.le delle Scienze Building 6, 90128 Palermo, Italy.
Ilenia VitranoEngineering Department, Università degli Studi di Palermo, V.le delle Scienze Building 6, 90128 Palermo, Italy.
Francesco Carfi PaviaEngineering Department, Università degli Studi di Palermo, V.le delle Scienze Building 6, 90128 Palermo, Italy.ORCID 0000-0001-5107-5588
Valerio BrucatoEngineering Department, Università degli Studi di Palermo, V.le delle Scienze Building 6, 90128 Palermo, Italy.ORCID 0000-0001-8309-5735
Vincenzo La CarrubbaEngineering Department, Università degli Studi di Palermo, V.le delle Scienze Building 6, 90128 Palermo, Italy.ORCID 0000-0002-3185-8398
Christian WernerInstitute of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, Prof. Ernst Nathan Str. 1, 90419 Nuremberg, Germany.
Kerstin Schäfer-EckartDepartment of Hematology, Klinikum Nürnberg, 90419 Nürnberg, Germany.
Gundula Schulze-TanzilInstitute of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, Prof. Ernst Nathan Str. 1, 90419 Nuremberg, Germany.ORCID 0000-0002-9807-9532
University of Palermo · ITParacelsus Medizinische Privatuniversität · DENuremberg Hospital · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bilayer scaffolds could provide a suitable topology for osteochondral defect repair mimicking cartilage and subchondral bone architecture. Hence, they could facilitate the chondro- and osteogenic lineage commitment of multipotent mesenchymal stromal cells (MSCs) with hydroxyapatite, the major inorganic component of bone, stimulating osteogenesis. Highly porous poly-L-lactic acid (PLLA) scaffolds with two layers of different pore sizes (100 and 250 µm) and hydroxyapatite (HA) supplementation were established by thermally induced phase separation (TIPS) to study growth and osteogenesis of human (h) MSCs. The topology of the scaffold prepared via TIPS was characterized using scanning electron microscopy (SEM), a microCT scan, pycnometry and gravimetric analysis. HMSCs and porcine articular chondrocytes (pACs) were seeded on the PLLA scaffolds without/with 5% HA for 1 and 7 days, and the cell attachment, survival, morphology, proliferation and gene expression of cartilage- and bone-related markers as well as sulfated glycosaminoglycan (sGAG) synthesis were monitored. All scaffold variants were cytocompatible, and hMSCs survived for the whole culture period. Cross-sections revealed living cells that also colonized inner scaffold areas, producing an extracellular matrix (ECM) containing sGAGs. The gene expression of cartilage and bone markers could be detected. HA represents a cytocompatible supplement in PLLA composite scaffolds intended for osteochondral defects.

Indexed as

chondrocyteschondrogenesishydroxyapatitemesenchymal stromal cellsosteochondral defectsosteogenesispoly-L-lactic acidtissue engineering

Identifiers

PMID38337220
PMCPMC10857361
OpenAlexW4391225226

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.