Evidence map›Paper›PMID 37830571›Full record

ArticleCells2023

An Efficient and Cost-Effective Approach to Generate Functional Human Inducible Pluripotent Stem Cell-Derived Astrocytes.

Hemil Gonzalez, Srinivas D Narasipura, Tanner Shull, Amogh Shetty, Tara L Teppen, Ankur Naqib, Lena Al-Harthi

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 4 institutions in 1 country.

Hemil GonzalezDepartment of Internal Medicine, Division of Infectious Diseases, Rush University Medical Center, Chicago, IL 60612, USA.
Srinivas D NarasipuraDepartment of Microbial Pathogens and Immunity, Rush Medical College, Chicago, IL 60612, USA.
Tanner ShullDepartment of Microbial Pathogens and Immunity, Rush Medical College, Chicago, IL 60612, USA.
Amogh ShettyIllinois Mathematics and Science Academy, Aurora, IL 60506, USA.
Tara L TeppenMolecular Neurobiology Division, Rush Alzheimer's Disease Center, Rush University, Chicago, IL 60612, USA.
Ankur NaqibGenome Core Facility, Rush University, Chicago, IL 60612, USA.
Lena Al-HarthiDepartment of Microbial Pathogens and Immunity, Rush Medical College, Chicago, IL 60612, USA.
Rush University · USIllinois Mathematics and Science Academy · USRush University Medical Center · USUniversity of Illinois Chicago · US

Funding

Dynamic interaction between HIV in the CNS and peripheral organsR01NS108796 · NINDS · RUSH UNIVERSITY MEDICAL CENTER · PI AL-HARTHI, LENA · 2019 to 2023
$3.7M
Human/Animal Brain Chimera in drugs of abuse and HIVR01DA055497 · NIDA · RUSH UNIVERSITY MEDICAL CENTER · PI Lena Al-Harthi · 2022 to 2026
$2.7M
NIDA NIH HHS R01 DA055497NINDS NIH HHS R01 NS108796
6 · The paper itself

Abstract

Human inducible pluripotent stem cell (hiPSC)-derived astrocytes (iAs) are critical to study astrocytes in health and disease. They provide several advantages over human fetal astrocytes in research, which include consistency, availability, disease modeling, customization, and ethical considerations. The generation of iAs is hampered by the requirement of Matrigel matrix coating for survival and proliferation. We provide a protocol demonstrating that human iAs cultured in the absence of Matrigel are viable and proliferative. Further, through a side-by-side comparison of cultures with and without Matrigel, we show significant similarities in astrocyte-specific profiling, including morphology (shape and structure), phenotype (cell-specific markers), genotype (transcriptional expression), metabolic (respiration), and functional aspects (glutamate uptake and cytokine response). In addition, we report that, unlike other CNS cell types, such as neuronal progenitor cells and neurons, iAs can withstand the absence of Matrigel coating. Our study demonstrates that Matrigel is dispensable for the culture of human iPSC-derived astrocytes, facilitating an easy, streamlined, and cost-effective method of generating these cells.

Indexed as

AstrocytesInduced Pluripotent Stem CellsCell DifferentiationCells, CulturedCost-Benefit AnalysisHumansastrocytesglutamate uptakeiAsiPSCmatrigelNPCseahorse

Identifiers

PMID37830571
PMCPMC10571578
OpenAlexW4387048241

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.