Evidence map›Paper›PMID 33859530›Full record

ArticleInternational journal of medical sciences2021

A novel 3D histotypic cartilage construct engineered by supercritical carbon dioxide decellularized porcine nasal cartilage graft and chondrocytes exhibited chondrogenic capability

Su-Shin Lee, Yi-Chia Wu, Shu-Hung Huang, Ying-Che Chen, Periasamy Srinivasan, Dar-Jen Hsieh, Yi-Chun Yeh, Yi-Ping Lai, Yun-Nan Lin

Abstract read
In one paragraph

Article in International journal of medical sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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  6. Reconstruction of the orbital floor using supercritical COInternational journal of medical 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

9 authors.

Su-Shin LeeDivision of Plastic Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.
Yi-Chia WuDivision of Plastic Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.
Shu-Hung HuangDivision of Plastic Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.
Ying-Che ChenDepartment of Surgery, Kaohsiung Municipal Siaogang Hospital, Kaohsiung, Taiwan.
Periasamy SrinivasanCenter of Research and Development, ACRO Biomedical Co., Ltd. Kaohsiung, Taiwan.
Dar-Jen HsiehCenter of Research and Development, ACRO Biomedical Co., Ltd. Kaohsiung, Taiwan.
Yi-Chun YehCenter of Research and Development, ACRO Biomedical Co., Ltd. Kaohsiung, Taiwan.
Yi-Ping LaiCenter of Research and Development, ACRO Biomedical Co., Ltd. Kaohsiung, Taiwan.
Yun-Nan LinDivision of Plastic Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Augmentative and reconstructive rhinoplasty surgical procedures use autologous tissue grafts or synthetic grafts to repair the nasal defect and aesthetic reconstruction. Donor site trauma and morbidity are common in autologous grafts. The desperate need for the production of grafted 3D cartilage tissues as rhinoplasty grafts without the adverse effect is the need of the hour. In the present study, we developed a bioactive 3D histotypic construct engineered with the various ratio of adipose-derived stem cells (ADSC) and chondrocytes together with decellularized porcine nasal cartilage graft (dPNCG). We decellularized porcine nasal cartilage using supercritical carbon dioxide (SCCO2) extraction technology. dPNCG was characterized by H&E, DAPI, alcian blue staining, scanning electron microscopy and residual DNA content, which demonstrated complete decellularization. 3D histotypic constructs were engineered using dPNCG, rat ADSC and chondrocytes with different percentage of cells and cultured for 21 days. dPNCG together with 100% chondrocytes produced a solid mass of 3D histotypic cartilage with significant production of glycosaminoglycans. H&E and alcian blue staining showed an intact mass, with cartilage granules bound to one another by extracellular matrix and proteoglycan, to form a 3D structure. Besides, the expression of chondrogenic markers, type II collagen, aggrecan and SOX-9 were elevated indicating chondrocytes cultured on dPNCG substrate facilitates the synthesis of type II collagen along with extracellular matrix to produce 3D histotypic cartilage. To conclude, dPNCG is an excellent substrate scaffold that might offer a suitable environment for chondrocytes to produce 3D histotypic cartilage. This engineered 3D construct might serve as a promising future candidate for cartilage tissue engineering in rhinoplasty.

Indexed as

AnimalsCarbon DioxideCells, CulturedChondrocytesChondrogenesisExtracellular MatrixHumansMesenchymal Stem CellsNasal CartilagesPrimary Cell CultureRatsRhinoplastySwineTissue EngineeringTissue ScaffoldsCarbon Dioxide3D histotypic cartilageadipose-derived stem cellschondrocytesdecellularized porcine nasal cartilage graft (dPNCG)supercritical carbon dioxide

Identifiers

PMID33859530
PMCPMC8040423

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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.