Evidence map›Paper›PMID 30781537›Full record

ArticleMaterials (Basel, Switzerland)2019

PLA-Based Mineral-Doped Scaffolds Seeded with Human Periapical Cyst-Derived MSCs: A Promising Tool for Regenerative Healing in Dentistry.

Marco Tatullo, Gianrico Spagnuolo, Bruna Codispoti, Fausto Zamparini, Anqi Zhang, Micaela Degli Esposti, Conrado Aparicio, Carlo Rengo, Manuel Nuzzolese, Lucia Manzoli and 4 more

Open access · goldAbstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 75 citations in OpenAlex.

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  16. Dental Pulp Stem Cell-Derived Secretome and Its Regenerative Potential.International journal of molecular sciences · 2021
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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

14 authors at 6 institutions in 3 countries.

Marco TatulloTecnologica Research Institute, Stem Cell Unit, 88900 Crotone, Italy. marco.tatullo@tecnologicasrl.com.ORCID 0000-0001-7340-0708
Gianrico SpagnuoloDepartment of Neurosciences, Reproductive and Odontostomatological Sciences, University of Naples "Federico II", 80131 Napoli, Italy. gianrico.spagnuolo@gmail.com.ORCID 0000-0003-3769-9786
Bruna CodispotiTecnologica Research Institute, Stem Cell Unit, 88900 Crotone, Italy. bruna.codispoti@tecnologicasrl.com.ORCID 0000-0001-8802-3546
Fausto ZampariniLaboratory of Biomaterials and Oral Pathology, School of Dentistry, Department of Biomedical and Neuromotor Sciences, University of Bologna, 40125 Bologna, Italy. fausto.zamparini2@unibo.it.ORCID 0000-0002-0071-4463
Anqi ZhangMDRCBB-Minnesota Dental Research Center for Biomaterials and Biomechanics, School of Dentistry, University of Minnesota, Minneapolis, MN 55455, USA. azhang@umn.edu.
Micaela Degli EspostiDepartment of Civil, Chemical, Environmental and Materials Engineering, University of Bologna, 40131 Bologna, Italy. micaela.degliesposti@unibo.it.
Conrado AparicioMDRCBB-Minnesota Dental Research Center for Biomaterials and Biomechanics, School of Dentistry, University of Minnesota, Minneapolis, MN 55455, USA. apari003@umn.edu.ORCID 0000-0003-2969-6067
Carlo RengoDepartment of Prosthodontics and Dental Materials, School of Dental Medicine, University of Siena, 53100 Siena, Italy. carlo.rengo@alice.it.
Manuel NuzzoleseUniversity Hospitals Birmingham-NHS Foundation Trust, Birmingham B152GW, UK. manuelnuzzolese@libero.it.
Lucia ManzoliCellular Signalling Laboratory, Institute of Human Anatomy, Department of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy. lucia.manzoli@unibo.it.
Fabio FavaDepartment of Civil, Chemical, Environmental and Materials Engineering, University of Bologna, 40131 Bologna, Italy. fabio.fava@unibo.it.
Carlo PratiLaboratory of Biomaterials and Oral Pathology, School of Dentistry, Department of Biomedical and Neuromotor Sciences, University of Bologna, 40125 Bologna, Italy. carlo.prati@unibo.it.
Paola FabbriDepartment of Civil, Chemical, Environmental and Materials Engineering, University of Bologna, 40131 Bologna, Italy. p.fabbri@unibo.it.
Maria Giovanna GandolfiLaboratory of Biomaterials and Oral Pathology, School of Dentistry, Department of Biomedical and Neuromotor Sciences, University of Bologna, 40125 Bologna, Italy. mgiovanna.gandolfi@unibo.it.
University of Bologna · ITIstituto S.Anna Crotone · ITUniversity of Minnesota · USUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity of Naples Federico II · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human periapical cyst mesenchymal stem cells (hPCy-MSCs) are a newly discovered cell population innovatively collected from inflammatory periapical cysts. The use of this biological waste guarantees a source of stem cells without any impact on the surrounding healthy tissues, presenting a valuable potential in tissue engineering and regenerative medicine applications. In the present study, hPCy-MSCs were collected, isolated, and seeded on three experimental mineral-doped porous scaffolds produced by the thermally-induced phase-separation (TIPS) technique. Mineral-doped scaffolds, composed of polylactic acid (PLA), dicalcium phosphate dihydrate (DCPD), and/or hydraulic calcium silicate (CaSi), were produced by TIPS (PLA-10CaSi, PLA-5CaSi-5DCPD, PLA-10CaSi-10DCPD). Micro-CT analysis evaluated scaffolds micromorphology. Collected hPCy-MSCs, characterized by cytofluorimetry, were seeded on the scaffolds and tested for cell proliferation, cells viability, and gene expression for osteogenic and odontogenic differentiation (DMP-1, OSC, RUNX-2, HPRT). Micro-CT revealed an interconnected highly porous structure for all the scaffolds, similar total porosity with 99% open pores. Pore wall thickness increased with the percentage of CaSi and DCPD. Cells seeded on mineral-doped scaffolds showed a superior proliferation compared to pure PLA scaffolds (control), particularly on PLA-10CaSi-10DCPD at day 12. A higher number of non-viable (red stained) cells was observable on PLA scaffolds at days 14 and 21. DMP-1 expression increased in hPCy-MSCs cultured on all mineral-doped scaffolds, in particular on PLA-5CaSi-5DCPD and PLA-10CaSi-10DCPD. In conclusion, the innovative combination of experimental scaffolds colonized with autologous stem cells from periapical cyst represent a promising strategy for regenerative healing of periapical and alveolar bone.

Indexed as

bioactive scaffoldscalcium silicate-containing scaffoldshuman periapical cyst mesenchymal stem cells (hPCy-MSCs)polylactic acid (PLA)-based scaffoldsporous scaffoldsregenerative dentistrythermally induced phase separation technique (TIPS)

Identifiers

PMID30781537
PMCPMC6416549
OpenAlexW2913784762

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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.