Evidence map›Paper›PMID 37405626›Full record

ArticleIn vitro cellular & developmental biology. Animal2023

Nanoscale vibration could promote tenogenic differentiation of umbilical cord mesenchymal stem cells.

Elahe Karimi, Negin Vahedi, Reza Ramezani Sarbandi, Azim Parandakh, Camellia Ganjoury, Faraz Sigaroodi, Najmeh Najmoddin, Mohammad Tabatabaei, Mohammad Tafazzoli-Shadpour, Abdolreza Ardeshirylajimi and 1 more

Abstract read
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In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

11 authors at 5 institutions in 2 countries.

Elahe KarimiDepartment of Tissue Engineering, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Negin VahediDepartment of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran, Iran.
Reza Ramezani SarbandiDepartment of Biomedical Engineering, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Azim ParandakhMedical Nanotechnology and Tissue Engineering Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Camellia GanjouryMedical Nanotechnology and Tissue Engineering Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Faraz SigaroodiDepartment of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Najmeh NajmoddinDepartment of Biomedical Engineering, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Mohammad TabatabaeiDepartment of Biomedical Engineering, Amirkabir University of Technology, Tehran, Iran.
Mohammad Tafazzoli-ShadpourDepartment of Biomedical Engineering, Amirkabir University of Technology, Tehran, Iran.
Abdolreza ArdeshirylajimiSina Cell Research and Product Center, Tehran, Iran.
Mohammad-Mehdi KhaniDepartment of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. khani@sbmu.ac.ir.
Shahid Beheshti University of Medical Sciences · IRIslamic Azad University, Science and Research Branch · IRAmirkabir University of Technology · IRSina Hospital · IRUniversity of Tehran · IR

Funding

Shahid Beheshti University of Medical Sciences 31747
6 · The paper itself

Abstract

Regulation of mesenchymal stem cell (MSC) fate for targeted cell therapy applications has been a subject of interest, particularly for tissues such as tendons that possess a marginal regenerative capacity. Control of MSCs' fate into the tendon-specific lineage has mainly been achieved by implementation of chemical growth factors. Mechanical stimuli or 3-dimensional (D) scaffolds have been used as an additional tool for the differentiation of MSCs into tenocytes, but oftentimes, they require a sophisticated bioreactor or a complex scaffold fabrication technique which reduces the feasibility of the proposed method to be used in practice. Here, we used nanovibration to induce the differentiation of MSCs toward the tenogenic fate solely by the use of nanovibration and without the need for growth factors or complex scaffolds. MSCs were cultured on 2D cell culture dishes that were connected to piezo ceramic arrays to apply nanovibration (30-80 nm and 1 kHz frequency) over 7 and 14 d. We observed that nanovibration resulted in significant overexpression of tendon-related markers in both gene expression and protein expression levels, while there was no significant differentiation into adipose and cartilage lineages. These findings could be of assistance in the mechanoregulation of MSCs for stem cell engineering and regenerative medicine applications.

Indexed as

Mesenchymal Stem CellsTissue EngineeringAnimalsCell DifferentiationUmbilical CordVibrationMechanotransductionMesenchymal stem cellsNanovibrationTendon regenerationTenogenic differentiation

Identifiers

PMID37405626
OpenAlexW4383186887

What Socratic holds

Textmetadata
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 Socratic graph.