Evidence map›Paper›PMID 32519278›Full record

ArticleCytotechnology2020

Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells.

Elena V Grigor'eva, Tuyana B Malankhanova, Aizhan Surumbayeva, Sophia V Pavlova, Julia M Minina, Elena A Kizilova, Lyubov A Suldina, Ksenia N Morozova, Elena Kiseleva, Eugeny D Sorokoumov and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Cytotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Generation of iPSCs from a Patient with the M694V Mutation in theInternational journal of molecular sciences · 2024
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  5. Article
  6. A Model of iPSC-Derived Macrophages withInternational journal of molecular sciences · 2023
    Article
  7. Article
  8. Biochemical Characteristics of iPSC-Derived Dopaminergic Neurons from N370SInternational journal of molecular sciences · 2023
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. 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

13 authors at 2 institutions in 1 country.

Elena V Grigor'evaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090. evlena@bionet.nsc.ru.ORCID http://orcid.org/0000-0002-9162-9108
Tuyana B MalankhanovaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.ORCID http://orcid.org/0000-0002-5106-8465
Aizhan SurumbayevaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.
Sophia V PavlovaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.ORCID http://orcid.org/0000-0003-1095-3692
Julia M MininaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.ORCID http://orcid.org/0000-0003-1504-9803
Elena A KizilovaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.
Lyubov A SuldinaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.
Ksenia N MorozovaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.ORCID http://orcid.org/0000-0003-3307-8819
Elena KiselevaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.ORCID http://orcid.org/0000-0001-6949-182X
Eugeny D SorokoumovFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.
Igor N LebedevResearch Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences, 5 Kooperativny Str, Tomsk, Russian Federation, 634050.
Suren M ZakianFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.ORCID http://orcid.org/0000-0003-2448-6511
Anastasia A MalakhovaFederal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, 10 Lavrentiev Ave, Novosibirsk, Russian Federation, 630090.ORCID http://orcid.org/0000-0003-1916-1333
Institute of Cytology and Genetics · RURussian Academy of Sciences · RU

Funding

Russian Science Foundation 16-15-10128
6 · The paper itself

Abstract

Cell models are promising tools for studying hereditary human neurodegenerative diseases. Neuronal derivatives of pluripotent stem cells provide the opportunity to investigate different stages of the neurodegeneration process. Therefore, easy and large-scale production of relevant cell types is a crucial barrier to overcome. In this work, we present an alternative protocol for iPSC differentiation into GABAergic medium spiny neurons (MSNs). The first stage involved dual-SMAD signalling inhibition through treatment with SB431542 and LDN193189, which results in the generation of neuroectodermal cells. Moreover, we used bFGF as a neuronal survival factor and dorsomorphin to inhibit BMP signalling. The combined treatment of dorsomorphin and SB431542 significantly enhanced neuronal induction, which was confirmed by the increased expression of the telencephalic-specific markers SOX1 and OTX2 as well as the forebrain marker PAX6. The next stage involved the derivation of actively proliferating MSN progenitor cells. An important feature of our protocol at this stage is the ability to perform prolonged cultivation of precursor cells at a high density without losing phenotypic properties. Moreover, the protocol enables multiple expansion steps (> 180 days cultivation) and cryopreservation of MSN progenitors. Therefore, this method allows quick production of a large number of neurons that are relevant for basic research, large-scale drug screening, and toxicological studies.

Indexed as

Induced pluripotent stem cellsMedium spiny neuronsNeuronal differentiationNeuronal precursors

Identifiers

PMID32519278
PMCPMC7547944
OpenAlexW3033881402

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.