Evidence map›Paper›PMID 33053753›Full record

ArticleBioengineering (Basel, Switzerland)2020

Mesenchymal Stem Cells Coated with Synthetic Bone-Targeting Polymers Enhance Osteoporotic Bone Fracture Regeneration.

Yuliya Safarova Yantsen, Farkhad Olzhayev, Bauyrzhan Umbayev, Andrey Tsoy, Gonzalo Hortelano, Tursonjan Tokay, Hironobu Murata, Alan Russell, Sholpan Askarova

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Yuliya Safarova YantsenLaboratory of Bioengineering and Regenerative Medicine, National Laboratory Astana, Nazarbayev University, Nur-Sultan 010000, Kazakhstan.ORCID 0000-0003-0695-0413
Farkhad OlzhayevLaboratory of Bioengineering and Regenerative Medicine, National Laboratory Astana, Nazarbayev University, Nur-Sultan 010000, Kazakhstan.
Bauyrzhan UmbayevLaboratory of Bioengineering and Regenerative Medicine, National Laboratory Astana, Nazarbayev University, Nur-Sultan 010000, Kazakhstan.ORCID 0000-0002-0286-7252
Andrey TsoyLaboratory of Bioengineering and Regenerative Medicine, National Laboratory Astana, Nazarbayev University, Nur-Sultan 010000, Kazakhstan.
Gonzalo HortelanoSchool of Sciences and Humanities, Nazarbayev University, Nur-Sultan 010000, Kazakhstan.
Tursonjan TokaySchool of Sciences and Humanities, Nazarbayev University, Nur-Sultan 010000, Kazakhstan.
Hironobu MurataDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Alan RussellDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Sholpan AskarovaLaboratory of Bioengineering and Regenerative Medicine, National Laboratory Astana, Nazarbayev University, Nur-Sultan 010000, Kazakhstan.ORCID 0000-0001-6161-1671

Funding

Ministry of Education and Science of the Republic of Kazakhstan 0118РК01040Nazarbayev University 091019CRP2113
6 · The paper itself

Abstract

Osteoporosis is a progressive skeletal disease characterized by reduced bone density leading to bone fragility and an elevated risk of bone fractures. In osteoporotic conditions, decrease in bone density happens due to the augmented osteoclastic activity and the reduced number of osteoblast progenitor cells (mesenchymal stem cells, MSCs). We investigated a new method of cell therapy with membrane-engineered MSCs to restore the osteoblast progenitor pool and to inhibit osteoclastic activity in the fractured osteoporotic bones. The primary active sites of the polymer are the N-hydroxysuccinimide and bisphosphonate groups that allow the polymer to covalently bind to the MSCs' plasma membrane, target hydroxyapatite molecules on the bone surface and inhibit osteolysis. The therapeutic utility of the membrane-engineered MSCs was investigated in female rats with induced estrogen-dependent osteoporosis and ulnar fractures. The analysis of the bone density dynamics showed a 27.4% and 21.5% increase in bone density at 4 and 24 weeks after the osteotomy of the ulna in animals that received four transplantations of polymer-modified MSCs. The results of the intravital observations were confirmed by the post-mortem analysis of histological slices of the fracture zones. Therefore, this combined approach that involves polymer and cell transplantation shows promise and warrants further bio-safety and clinical exploration.

Indexed as

bone fracturemesenchymal stem cellsosteoporosistargeted cell delivery

Identifiers

PMID33053753
PMCPMC7711537

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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.