Evidence map›Paper›PMID 33471211›Full record

ArticleJournal of materials science. Materials in medicine2021

Characterization and cytocompatibility of 3D porous biomimetic scaffold derived from rabbit nucleus pulposus tissue in vitro.

Yu Zhang, Wei Tan, Mingxin Wu, Jin Sun, Wei Cao, Chu-Song Zhou, You Wu

Abstract read
In one paragraph

Article in Journal of materials science. Materials in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

7 authors.

Yu ZhangDepartment of Orthopaedics, General Hospital of Southern Theatre Command of PLA, Guangzhou, 510010, Guangdong, PR China.
Wei TanDepartment of Spinal Orthopedics, Huizhou Third People's Hospital, Guangzhou Medical University, Huizhou, 516002, Guangdong, PR China.ORCID http://orcid.org/0000-0002-5739-2258
Mingxin WuDepartment of Spinal Orthopedics, Huizhou Third People's Hospital, Guangzhou Medical University, Huizhou, 516002, Guangdong, PR China.
Jin SunDepartment of Spinal Orthopedics, Huizhou Third People's Hospital, Guangzhou Medical University, Huizhou, 516002, Guangdong, PR China. 824061581@qq.com.
Wei CaoDepartment of Spinal Orthopedics, The first people's hospital of Huaihua, Huaihua, 418000, Hunan, PR China.
Chu-Song ZhouDepartment of Orthopaedics, Zhu-Jiang Hospital of Southern Medical University (First Military Medical University), Guangzhou, 510282, Guangdong, PR China. mdzcs28@163.com.
You WuDepartment of Orthopaedics, General Hospital of Southern Theatre Command of PLA, Guangzhou, 510010, Guangdong, PR China.

Funding

Guangzhou Municipal Science and Technology Program 2014J4100131
6 · The paper itself

Abstract

Intervertebral disc (IVD) degeneration is one of the most important causes of lower back pain. Tissue engineering provides a new method for the experimental treatment of degenerative disc diseases. This study aims to develop a natural, acellular, 3D interconnected porous scaffold derived from the extracellular matrix (ECM) of nucleus pulposus. The nucleus pulposus (NP) was decellularized by sequential detergent-nuclease methods, including physical crushing, freeze-drying and cross-linking. These 3D porous scaffolds were fabricated with a high porosity of (81.28 ± 4.10)%, an ideal pore size with appropriate mechanical properties. Rabbit bone marrow mesenchymal stem cells (rBMSCs) were seeded and cultured on the scaffolds. And the mechanical tests showed the compressive elastic modulus of the scaffolds cultured for 4 weeks reached 0.12 MPa, which was better than that of the scaffolds cultured for 2 weeks (0.07 MPa) and that of the control group (0.04 MPa). Scanning electron microscopy (SEM), histological assays, molecular biology assays revealed that the scaffolds could provide an appropriate microstructure and environment for the adhesion, proliferation, migration and secretion of seeded cells in vitro. As assays like histology, immunohistochemistry and the real-time qRT-PCR showed, NP-like tissues were preliminarily formed. In conclusion, the 3D porous scaffold derived from NP ECM is a potential biomaterial for the regeneration of NP tissues. A natural, acellular, 3D interconnected porous scaffold derived from the extracellular matrix (ECM) of nucleus pulposus was developed by sequential detergent-nuclease and freeze-drying method, which can reduce the damage of protein activity to the minimum. It is very similar to the composition and internal environment of the natural nucleus pulposus, because it derived from the natural nucleus pulposus. Scanning electron microscopy (SEM), histological assays, molecular biology assays revealed that the scaffolds could provide an appropriate microstructure and environment for the adhesion, proliferation, migration, and secretion of seeded cells in vitro.

Indexed as

BiomimeticsAnimalsBiocompatible MaterialsBone Marrow CellsCell Culture TechniquesCell ProliferationCell SurvivalExtracellular MatrixMesenchymal Stem CellsMicroscopy, Electron, ScanningMicroscopy, FluorescenceNucleus PulposusPorosityPressureRabbitsStress, MechanicalBiocompatible MaterialsTetrazolium SaltsThiazolesthiazolyl blue

Identifiers

PMID33471211
PMCPMC7817588

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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.