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Membrane Biophysics Define Neuron and Astrocyte Progenitors in the Neural Lineage
Author(s) -
Nourse J.L.,
Prieto J.L.,
Dickson A.R.,
Lu J.,
Pathak M.M.,
Tombola F.,
Demetriou M.,
Lee A.P.,
Flanagan L.A.
Publication year - 2014
Publication title -
stem cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.159
H-Index - 229
eISSN - 1549-4918
pISSN - 1066-5099
DOI - 10.1002/stem.1535
Subject(s) - progenitor cell , biology , neural stem cell , microbiology and biotechnology , stem cell , electrophysiology , cell sorting , progenitor , cell , neuroscience , biochemistry
Neural stem and progenitor cells (NSPCs) are heterogeneous populations of self‐renewing stem cells and more committed progenitors that differentiate into neurons, astrocytes, and oligodendrocytes. Accurately identifying and characterizing the different progenitor cells in this lineage has continued to be a challenge for the field. We found previously that populations of NSPCs with more neurogenic progenitors (NPs) can be distinguished from those with more astrogenic progenitors (APs) by their inherent biophysical properties, specifically the electrophysiological property of whole cell membrane capacitance, which we characterized with dielectrophoresis (DEP). Here, we hypothesize that inherent electrophysiological properties are sufficient to define NPs and APs and test this by determining whether isolation of cells solely by these properties specifically separates NPs and APs. We found NPs and APs are enriched in distinct fractions after separation by electrophysiological properties using DEP. A single round of DEP isolation provided greater NP enrichment than sorting with PSA‐NCAM, which is considered an NP marker. Additionally, cell surface N‐linked glycosylation was found to significantly affect cell fate‐specific electrophysiological properties, providing a molecular basis for the cell membrane characteristics. Inherent plasma membrane biophysical properties are thus sufficient to define progenitor cells of differing fate potential in the neural lineage, can be used to specifically isolate these cells, and are linked to patterns of glycosylation on the cell surface. S tem C ells 2014;32:706–716

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