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Unique dielectric properties distinguish stem cells and their differentiated progeny.

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TLDR
Evidence is provided for a whole cell property that reflects stem cell fate bias and DEP is established as a tool with unique capabilities for interrogating, characterizing, and sorting stem cells.
Abstract
The relatively new field of stem cell biology is hampered by a lack of sufficient means to accurately determine the phenotype of cells. Cell-type-specific markers, such as cell surface proteins used for flow cytometry or fluorescence-activated cell sorting, are limited and often recognize multiple members of a stem cell lineage. We sought to develop a complementary approach that would be less dependent on the identification of particular markers for the subpopulations of cells and would instead measure their overall character. We tested whether a microfluidic system using dielectrophoresis (DEP), which induces a frequency-dependent dipole in cells, would be useful for characterizing stem cells and their differentiated progeny. We found that populations of mouse neural stem/precursor cells (NSPCs), differentiated neurons, and differentiated astrocytes had different dielectric properties revealed by DEP. By isolating NSPCs from developmental ages at which they are more likely to generate neurons, or astrocytes, we were able to show that a shift in dielectric property reflecting their fate bias precedes detectable marker expression in these cells and identifies specific progenitor populations. In addition, experimental data and mathematical modeling suggest that DEP curve parameters can indicate cell heterogeneity in mixed cultures. These findings provide evidence for a whole cell property that reflects stem cell fate bias and establish DEP as a tool with unique capabilities for interrogating, characterizing, and sorting stem cells.

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Journal ArticleDOI

Review Article—Dielectrophoresis: Status of the theory, technology, and applications

TL;DR: Current trends suggest that the theory and technology have matured sufficiently for most effort to now be directed towards applying DEP to unmet needs in such areas as biosensors, cell therapeutics, drug discovery, medical diagnostics, microfluidics, nanoassembly, and particle filtration.
Journal ArticleDOI

Role of Membrane Potential in the Regulation of Cell Proliferation and Differentiation

TL;DR: Understanding the molecular and mechanistic basis of biophysical regulation will point the way toward novel ways to rationally direct cell functions, allowing us to capitalize upon the potential ofBiophysical signaling for regenerative medicine and tissue engineering.
Journal ArticleDOI

Complex and dynamic landscape of RNA polyadenylation revealed by PAS-Seq

TL;DR: PAS-Seq analyses revealed a complex landscape of RNA polyadenylation in mammalian cells and the dynamic regulation of APA during stem cell differentiation and detected significant changes in the global APA profile that lead to lengthening of 3' untranslated regions (UTR) in many mRNAs during stem Cell differentiation.
Journal ArticleDOI

Dielectrophoresis in microfluidics technology

TL;DR: In this review, a detailed analysis of the modeling of DEP‐based manipulation of the particles is provided, and the recent applications regarding the particle manipulation in microfluidic systems are presented.
Journal ArticleDOI

Cellular dielectrophoresis: applications to the characterization, manipulation, separation and patterning of cells.

TL;DR: There is need for a critical report to integrate the many new features ofDEP for cellular applications, and a review of the basic theory and current applications of DEP, specifically for cells is presented.
References
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Journal ArticleDOI

Subventricular Zone Astrocytes Are Neural Stem Cells in the Adult Mammalian Brain

TL;DR: It is shown that SVZ astrocytes act as neural stem cells in both the normal and regenerating brain and give rise to cells that grow into multipotent neurospheres in vitro.
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A multipotent EGF-responsive striatal embryonic progenitor cell produces neurons and astrocytes.

TL;DR: It is suggested that EGF and/or TGF alpha may act on a multipotent progenitor cell in the striatum to generate both neurons and astrocytes.
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Isolation of radial glial cells by fluorescent-activated cell sorting reveals a neuronal lineage.

TL;DR: Using fluorescence-activated cell sorting, it is shown that radial glial cells also are neuronal precursors and only later, after neurogenesis, do they shift towards an exclusive generation of astrocytes.
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Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age

TL;DR: Although deficiencies in several genomic maintenance pathways did not deplete stem cell reserves with age, stem cell functional capacity was severely affected under conditions of stress, leading to loss of reconstitution and proliferative potential, diminished self-renewal, increased apoptosis and, ultimately, functional exhaustion.
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Distinct neural stem cells proliferate in response to EGF and FGF in the developing mouse telencephalon.

TL;DR: The results support a model in which separate, lineage-related EGF- and FGF-responsive neural stem cells are present in the embryonic telencephalic germinal zone, and show that EGF alone and F GF2 alone can independently elicit neural stem cell proliferation and at relatively high cell densities separate cell nonautonomous effects can substantially enhance the mitogen-induced proliferation.
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