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Culturing and Imaging Glioma Stem Cells in 3D Collagen Matrices
James M. Cowan
,
Matey Juric
and
Ryan J. Petrie
Show details for 3 authors
Current protocols, v 3(1), pp e643-n/a
Jan 2023
DOI:
https://doi.org/10.1002/cpz1.643
PMID: 36598361
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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830581
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Abstract
collagen
culture
glioma
microscopy
migration
Methods to maintain human glioma stem cells as neurosphere cultures and image their dynamic behavior in 3D collagen matrices are described. Additional approaches to monitor glioma stem cell differentiation into mesenchymal‐type cells, along with example data are included. Together, these approaches enable glioma stem cell differentiation to be controlled while maintaining the cells in culture, as well as allowing cell dynamics to be captured and analyzed. These methods should be helpful for those seeking to understand the molecular mechanisms driving the invasion of glioma cells through three‐dimensional environments. © 2023 Wiley Periodicals LLC. Basic Protocol 1: Culturing human glioma stem cells as neurospheres Basic Protocol 2: Inducing GSC adherence and monitoring their differentiation into mesenchymal cells Support Protocol 1: Preparing fibronectin‐coated dishes for cell microscopy Basic Protocol 3: Embedding GSCs in a 3D collagen matrix to study their invasive behavior Support Protocol 2: Phase‐contrast imaging with a tiled matrix to study cell migration in a 3D gel
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Title
Culturing and Imaging Glioma Stem Cells in 3D Collagen Matrices
Creators
James M. Cowan - Drexel University
Matey Juric - Drexel University
Ryan J. Petrie - Drexel University
Publication Details
Current protocols, v 3(1), pp e643-n/a
Publisher
Wiley
Number of pages
25
Resource Type
Journal article
Language
English
Academic Unit
Biology
Scopus ID
2-s2.0-85145641483
Other Identifier
991020099380604721
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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830581
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