Evidence map›Paper›PMID 37508556›Full record

ArticleCells2023

Differentiation Induction of Mesenchymal Stem Cells by a Au Delivery Platform.

Meng-Yin Yang, Cheng-Di Chiu, Yi-Chun Ke, Yi-Chin Yang, Kai-Bo Chang, Chien-Min Chen, Hsu-Tung Lee, Chien-Lun Tang, Bai-Shuan Liu, Huey-Shan Hung

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 73% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 5 institutions in 1 country.

Meng-Yin YangDepartment of Neurosurgery, Neurological Institute, Taichung Veterans General Hospital, Taichung 407219, Taiwan.ORCID 0000-0002-2544-8181
Cheng-Di ChiuDepartment of Neurosurgery, China Medical University Hospital, Taichung 404327, Taiwan.ORCID 0000-0003-0369-0935
Yi-Chun KeGraduate Institute of Biomedical Science, China Medical University, Taichung 404333, Taiwan.
Yi-Chin YangDepartment of Neurosurgery, Neurological Institute, Taichung Veterans General Hospital, Taichung 407219, Taiwan.ORCID 0000-0002-9651-3761
Kai-Bo ChangGraduate Institute of Biomedical Science, China Medical University, Taichung 404333, Taiwan.
Chien-Min ChenDivision of Neurosurgery, Department of Surgery, Changhua Christian Hospital, Changhua 50006, Taiwan.
Hsu-Tung LeeDepartment of Neurosurgery, Neurological Institute, Taichung Veterans General Hospital, Taichung 407219, Taiwan.
Chien-Lun TangDepartment of Neurosurgery, Neurological Institute, Taichung Veterans General Hospital, Taichung 407219, Taiwan.
Bai-Shuan LiuDepartment of Medical Imaging and Radiological Sciences, Central Taiwan University of Science and Technology, Taichung 406053, Taiwan.
Huey-Shan HungGraduate Institute of Biomedical Science, China Medical University, Taichung 404333, Taiwan.ORCID 0000-0003-4161-2428
China Medical University · TWNational Chung Hsing University · TWTaichung Veterans General Hospital · TWCentral Taiwan University of Science and Technology · TWChanghua Christian Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Au decorated with type I collagen (Col) was used as a core material to cross-link with stromal cell-derived factor 1α (SDF1α) in order to investigate biological performance. The Au-based nanoparticles were subjected to physicochemical determination using scanning electron microscopy (SEM), dynamic light scattering (DLS) and ultraviolet-visible (UV-Vis) and Fourier-transform infrared spectroscopy (FTIR). Mesenchymal stem cells (MSCs) were used to evaluate the biocompatibility of this nanoparticle using the MTT assay and measuring reactive oxygen species (ROS) production. Also, the biological effects of the SDF-1α-conjugated nanoparticles (Au-Col-SDF1α) were assessed and the mechanisms were explored. Furthermore, we investigated the cell differentiation-inducing potential of these conjugated nanoparticles on MSCs toward endothelial cells, neurons, osteoblasts and adipocytes. We then ultimately explored the process of cell entry and transportation of the nanoparticles. Using a mouse animal model and retro-orbital sinus injection, we traced in vivo biodistribution to determine the biosafety of the Au-Col-SDF1α nanoparticles. In summary, our results indicate that Au-Col is a promising drug delivery system; it can be used to carry SDF1α to improve MSC therapeutic efficiency.

Indexed as

Mesenchymal Stem CellsNanoparticlesAnimalsCell DifferentiationEndothelial CellsTissue DistributionAudifferentiationdrug deliverymesenchymal stem cellstromal cell-derived factor 1α

Identifiers

PMID37508556
PMCPMC10378595
OpenAlexW4384932091

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.