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