Evidence map›Paper›PMID 29945671›Full record

ArticleStem cell research & therapy2018

Pericellular collagen I coating for enhanced homing and chondrogenic differentiation of mesenchymal stem cells in direct intra-articular injection.

Hansong Xia, Chi Liang, Pan Luo, Junjie Huang, Jinshen He, Zili Wang, Xu Cao, Cheng Peng, Song Wu

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Hansong XiaDepartment of Orthopaedics, 3rd Xiangya Hospital, Central South University, Changsha, 410013, China.
Chi LiangDepartment of Orthopaedics, 3rd Xiangya Hospital, Central South University, Changsha, 410013, China.
Pan LuoDepartment of Orthopaedics, 3rd Xiangya Hospital, Central South University, Changsha, 410013, China.
Junjie HuangDepartment of Orthopaedics, 3rd Xiangya Hospital, Central South University, Changsha, 410013, China.
Jinshen HeDepartment of Orthopaedics, 3rd Xiangya Hospital, Central South University, Changsha, 410013, China.
Zili WangDepartment of Orthopaedics, 3rd Xiangya Hospital, Central South University, Changsha, 410013, China.
Xu CaoDepartment of Orthopaedics, 3rd Xiangya Hospital, Central South University, Changsha, 410013, China. hughcaoxu@hotmail.com.
Cheng PengDepartment of Burns and Plastic Surgery, 3rd Xiangya Hospital, Central South University, Changsha, 410013, China. pcheng83@sina.com.
Song WuDepartment of Orthopaedics, 3rd Xiangya Hospital, Central South University, Changsha, 410013, China. swhn9058@163.com.
Central South University · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDirect intra-articular injection (DIAI) of mesenchymal stem cells (MSCs) is a promising technique for cartilage repair. However, the repair process was hindered by the absence of scaffold and poor cell-matrix interactions.

methodsIn this study, we developed a pericellular collagen I coating (PCC) on MSCs. The overall performances of MSC-PCC homing, chondrogenic differentiation, and cartilage regeneration have been comprehensively evaluated in a New Zealand rabbit model. Firstly, we examined the morphology and physical characteristics of PCC. Secondly, MSC ex-vivo cartilage slice adhesion and in-vivo cartilage defect homing were observed using multiscale methods. Thirdly, the precartilage condensation of cell pellets formed by aggregation of MSCs was examined to evaluate the cartilage-inducing potential of PCC. Finally, the cartilage regeneration by DIAI of PCC-coated MSCs was observed and scored macroscopically and histologically.

resultsIn general, the cell adhesion and homing assay revealed that PCC facilitated MSC adhesion on cartilage slices, enhancing MSC homing and retention to cartilage defect. This increased homing ratio was accompanied by an increasing cell-cell contact. Compared with naked MSCs, the cell pellets formed by PCC-coated MSCs exhibited more evident appearance of condensation. In pellets, cell-cell interaction has been significantly stimulated, inducing the expression of condensation marker N-cadherin, and subsequent chondrogenic marker collagen II and aggrecan. By 12 weeks after DIAI, cartilage defects have been repaired by MSCs to varying degrees. Overall, PCC significantly enhances the quality of cartilage regeneration judging from macroscopic observation, ICRS score, histological examination, and collagen type I, II, and X immunohistochemical staining.

conclusionsThe capacity and viability of MSCs can be enhanced by collagen I coating, which provides cues for enhancing cell homing and differentiation. Our method provides a novel strategy for stem cell therapy.

Indexed as

Cartilage, ArticularCell DifferentiationCells, CulturedChondrogenesisCollagen Type IHumansInjections, Intra-ArticularMesenchymal Stem CellsCollagen Type IBone marrow mesenchymal stem cellsCartilage injuryCartilage repairChondrogenic differentiationHoming

Identifiers

PMID29945671
PMCPMC6020325
OpenAlexW2810664556

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LicenceCC BY
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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.