Evidence map›Paper›PMID 26234712›Full record

ArticleScientific reports2015

A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells.

Doo Yeon Kwon, Jin Seon Kwon, Seung Hun Park, Ji Hun Park, So Hee Jang, Xiang Yun Yin, Jeong-Ho Yun, Jae Ho Kim, Byoung Hyun Min, Jun Hee Lee and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

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  8. The role of proteoglycan form of DMP1 in cranial repair.BMC molecular and cell biology · 2022
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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

12 authors at 3 institutions in 1 country.

Doo Yeon KwonDepartment of Molecular Science and Technology, Ajou University, Suwon 443-759, Korea.
Jin Seon KwonDepartment of Molecular Science and Technology, Ajou University, Suwon 443-759, Korea.
Seung Hun ParkDepartment of Molecular Science and Technology, Ajou University, Suwon 443-759, Korea.
Ji Hun ParkDepartment of Molecular Science and Technology, Ajou University, Suwon 443-759, Korea.
So Hee Jang1] Department of Molecular Science and Technology, Ajou University, Suwon 443-759, Korea [2] Nature-Inspired Mechanical System Team, Korea Institute of Machinery and Materials, Daejeon 305-343, Korea.
Xiang Yun YinDepartment of Molecular Science and Technology, Ajou University, Suwon 443-759, Korea.
Jeong-Ho YunDepartment of Dentistry, School of Medicine, Inha University, Incheon 440-711, Korea.
Jae Ho KimDepartment of Molecular Science and Technology, Ajou University, Suwon 443-759, Korea.
Byoung Hyun MinDepartment of Molecular Science and Technology, Ajou University, Suwon 443-759, Korea.
Jun Hee LeeNature-Inspired Mechanical System Team, Korea Institute of Machinery and Materials, Daejeon 305-343, Korea.
Wan-Doo KimNature-Inspired Mechanical System Team, Korea Institute of Machinery and Materials, Daejeon 305-343, Korea.
Moon Suk KimDepartment of Molecular Science and Technology, Ajou University, Suwon 443-759, Korea.
Ajou University · KRKorea Institute of Machinery and Materials · KRInha University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A computer-designed, solvent-free scaffold offer several potential advantages such as ease of customized manufacture and in vivo safety. In this work, we firstly used a computer-designed, solvent-free scaffold and human dental pulp stem cells (hDPSCs) to regenerate neo-bone within cranial bone defects. The hDPSCs expressed mesenchymal stem cell markers and served as an abundant source of stem cells with a high proliferation rate. In addition, hDPSCs showed a phenotype of differentiated osteoblasts in the presence of osteogenic factors (OF). We used solid freeform fabrication (SFF) with biodegradable polyesters (MPEG-(PLLA-co-PGA-co-PCL) (PLGC)) to fabricate a computer-designed scaffold. The SFF technology gave quick and reproducible results. To assess bone tissue engineering in vivo, the computer-designed, circular PLGC scaffold was implanted into a full-thickness cranial bone defect and monitored by micro-computed tomography (CT) and histology of the in vivo tissue-engineered bone. Neo-bone formation of more than 50% in both micro-CT and histology tests was observed at only PLGC scaffold with hDPSCs/OF. Furthermore, the PLGC scaffold gradually degraded, as evidenced by the fluorescent-labeled PLGC scaffold, which provides information to tract biodegradation of implanted PLGC scaffold. In conclusion, we confirmed neo-bone formation within a cranial bone defect using hDPSCs and a computer-designed PLGC scaffold.

Indexed as

Bone RegenerationTissue ScaffoldsAdultAnimalsBiocompatible MaterialsCell DifferentiationCell ProliferationComputer-Aided DesignDental PulpFemaleHumansOsteoblastsPolyestersRats, Sprague-DawleySkullStem CellsBiocompatible MaterialsPolyesterspoly(L-lactide-co-glycolide-co-epsilon-caprolactone)

Identifiers

PMID26234712
PMCPMC4522608
OpenAlexW1511534740

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.