Evidence map›Paper›PMID 34033079›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2021

Preparation of Neural Stem Cells and Progenitors: Neuronal Production and Grafting Applications.

Lyandysha V Zholudeva, Ying Jin, Liang Qiang, Michael A Lane, Itzhak Fischer

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
5.7field-weighted citation impact, top 3% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Cell transplantation to repair the injured spinal cord.International review of neurobiology · 2022
    Article
  9. 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

5 authors at 1 institution in 1 country.

Lyandysha V ZholudevaDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA.
Ying JinDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA.
Liang QiangDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA.
Michael A LaneDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA.
Itzhak FischerDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA. if24@drexel.edu.
Drexel University · US

Funding

SurgeryP01NS055976 · NINDS · DREXEL UNIVERSITY · PI TOM, VERONICA JEAN · 2007 to 2017
$12.3M
Neural transplants to promote respiratory plasticity after spinal cord injuryR01NS104291 · NINDS · DREXEL UNIVERSITY · PI LANE, MICHAEL ARON · 2018 to 2022
$1.7M
NINDS NIH HHS P01 NS055976NINDS NIH HHS R01 NS104291
6 · The paper itself

Abstract

Neural stem cells (NSCs) are a valuable tool for the study of neural development and function as well as an important source of cell transplantation strategies for neural disease. NSCs can be used to study how neurons acquire distinct phenotypes and how the interactions between neurons and glial cells in the developing nervous system shape the structure and function of the CNS. NSCs can also be used for cell replacement therapies following CNS injury targeting astrocytes, oligodendrocytes, and neurons. With the availability of patient-derived induced pluripotent stem cells (iPSCs), neurons prepared from NSCs can be used to elucidate the molecular basis of neurological disorders leading to potential treatments. Although NSCs can be derived from different species and many sources, including embryonic stem cells (ESCs), iPSCs, adult CNS, and direct reprogramming of nonneural cells, isolating primary NSCs directly from fetal tissue is still the most common technique for preparation and study of neurons. Regardless of the source of tissue, similar techniques are used to maintain NSCs in culture and to differentiate NSCs toward mature neural lineages. This chapter will describe specific methods for isolating and characterizing multipotent NSCs and neural precursor cells (NPCs) from embryonic rat CNS tissue (mostly spinal cord) and from human ESCs and iPSCs as well as NPCs prepared by reprogramming. NPCs can be separated into neuronal and glial restricted progenitors (NRP and GRP, respectively) and used to reliably produce neurons or glial cells both in vitro and following transplantation into the adult CNS. This chapter will describe in detail the methods required for the isolation, propagation, storage, and differentiation of NSCs and NPCs isolated from rat and mouse spinal cords for subsequent in vitro or in vivo studies as well as new methods associated with ESCs, iPSCs, and reprogramming.

Indexed as

NeurogenesisAnimalsCell Culture TechniquesCell LineageCell ProliferationCells, CulturedCell SeparationCell SurvivalCellular ReprogrammingCellular Reprogramming TechniquesFemaleGene Expression Regulation, DevelopmentalGestational AgeHumansInduced Pluripotent Stem CellsMiceCell transplantationEmbryonic stem cellsInduces pluripotent cellsNeural progenitor cellsNeuronsSpinal cord injury

Identifiers

PMID34033079
PMCPMC10074836
OpenAlexW3164885895

What OpenQuestion holds

Textmetadata
LicenceTDM
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.