Evidence map›Paper›PMID 30880567›Full record

ArticleCell cycle (Georgetown, Tex.)

Optimization of lentiviral transduction parameters and its application for CRISPR-based secretome modification of human endometrial mesenchymal stem cells.

Pavel Deryabin, Anastasiia Griukova, Alla Shatrova, Alexey Petukhov, Nikolay Nikolsky, Aleksandra Borodkina

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. A platform to deliver single and bi-specific Cas9/guide RNA to perturb genes in vitro and in vivo.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
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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

6 authors at 2 institutions in 1 country.

Pavel Deryabina Institute of Cytology , Russian Academy of Sciences , Saint-Petersburg , Russia.ORCID 0000-0003-2451-2943
Anastasiia Griukovaa Institute of Cytology , Russian Academy of Sciences , Saint-Petersburg , Russia.ORCID 0000-0001-5283-4144
Alla Shatrovaa Institute of Cytology , Russian Academy of Sciences , Saint-Petersburg , Russia.ORCID 0000-0002-4410-9580
Alexey Petukhova Institute of Cytology , Russian Academy of Sciences , Saint-Petersburg , Russia.ORCID 0000-0002-7298-5238
Nikolay Nikolskya Institute of Cytology , Russian Academy of Sciences , Saint-Petersburg , Russia.
Aleksandra Borodkinaa Institute of Cytology , Russian Academy of Sciences , Saint-Petersburg , Russia.
Institute of Cytology · RUFederal Almazov North-West Medical Research Centre · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) hold a great promise for successful development of regenerative medicine. Among the plenty of uncovered MSCs sources, desquamated endometrium collected from the menstrual blood probably remains the most accessible. Though numerous studies have been published on human endometrium-derived mesenchymal stem cells (hMESCs) properties in the past years, there are only a few data regarding their genetic modulation. Moreover, there is a lack of information about the fate of the transduced hMESCs. The present study aimed to optimize hMESCs transduction parameters and apply Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 technology for genome and secretome modification. The fate of hMESCs transduced either in presence of polybrene (Pb) or protamine sulfate (Ps) was assessed by alterations in CD expression profile, growth rate, cell size, migration capability, osteogenic, adipogenic, and decidual differential potentials. Here, we postulated that the use of Ps for hMESCs genetic manipulations is preferable, as it has no impact on the stem-cell properties, whereas Pb application is undesirable, as it induces cellular senescence. Plasminogen activator inhibitor-1 was selected for further targeted hMESCs genome and secretome modification using CRISPR/Cas9 systems. The obtained data provide optimized transduction scheme for hMESCs and verification of its effectiveness by successful hMESCs genome editing via CRISPR/Cas9 technology.

Indexed as

Cells, CulturedCellular SenescenceClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsEndometriumFemaleGene EditingGenetic TherapyGenomeHEK293 CellsHumansLentivirusMesenchymal Stem CellsRegenerative MedicineCRISPR/Cas9 engineeringgene editingHuman endometrium-derived mesenchymal stem cellslentiviral transductionPAI-1/SERPINE 1secretome modificationsenescence

Identifiers

PMID30880567
PMCPMC6464586
OpenAlexW2921080785

What OpenQuestion 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 OpenQuestion graph.