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Volume Measurements in Cultured Primary Astrocytes

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In Vitro Neurotoxicology

Part of the book series: Methods in Molecular Biology ((MIMB,volume 758))

Abstract

Damage to the central nervous system (CNS) is selective, likely reflecting the intrinsic properties of ­individual cell types. Targets of chemical injury are diverse hence assessing neurotoxicity is extremely difficult. Overcoming this obstacle requires a general screen or “marker” for injury that reflects cellular damage. The “marker” must be reliable and represent a biochemical event which broadly reflects cellular stress and damage. One such “marker” is cell swelling; it occurs in response to a diversity of insults, such as physical damage, disease (ischemia, trauma, and hypoxia), and chemicals (methylmercury, lead, 1,3-dinitrobenzene, and triethyltin). In astrocytes, a type of glia, astrocytic swelling can be measured with several methods. Commonly, freshly isolated astrocytes are grown to confluence on coverslips, a period requiring 3 weeks in culture. At this time, astrocytic volume can be measured using either an impedance technique or 3-O-methyl-d-glucose to assess cell volume. This review will briefly detail these methods and provide insight into molecular mechanisms associated with cell swelling and the ensuing regulatory decrease (RVD).

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Acknowledgments

Financial support from PHS NIH grants NIEHS 07331 and 10563 is gratefully acknowledged.

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Correspondence to Michael Aschner .

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Aschner, M. (2011). Volume Measurements in Cultured Primary Astrocytes. In: Costa, L., Giordano, G., Guizzetti, M. (eds) In Vitro Neurotoxicology. Methods in Molecular Biology, vol 758. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-61779-170-3_26

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  • DOI: https://doi.org/10.1007/978-1-61779-170-3_26

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  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-61779-169-7

  • Online ISBN: 978-1-61779-170-3

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