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Freeze-drying of unfixed monolayer cultures for electron microscopic autoradiography

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Summary

A method has been developed for freezing, drying and embedding of unfixed monolayer cultures for electron microscopic autoradiography (EM ARG). Experimental results showed: a) Aclar 33 C was a more suitable substrate than the plastic of petri dishes, b) cultures pressed rapidly against the polished face of a large copper cylinder chilled in liquid nitrogen had better cellular morphology than did cultures dipped in Freon 12 chilled in liquid nitrogen, and c) cultures embedded in Epon alone had finer extracellular ice spaces and lower background grain densities than did cultures embedded in Epon with 1% silicone.

This method has been used to evaluate the effect of fixation on the localization of the neurotransmitter, 3H-gamma-aminobutyric acid (3H-GABA), in neurons of dispersed cell cultures. EM ARG results showed that the neuronal cell bodies and vesicle elements were present in similar numbers in both glutaraldehyde fixed and freeze-dried cultures.

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Authors and Affiliations

  1. Department of Anatomy, School of Medicine University of Colorado, Denver, Colorado, USA

    R. W. Burry & R. S. Lasher

  2. Department of Anatomy, University of Tennessee Center for the Health Sciences, Memphis, Tennessee, USA

    R. W. Burry

Authors
  1. R. W. Burry
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  2. R. S. Lasher
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Burry, R.W., Lasher, R.S. Freeze-drying of unfixed monolayer cultures for electron microscopic autoradiography. Histochemistry 58, 259–272 (1978). https://doi.org/10.1007/BF00495382

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  • DOI: https://doi.org/10.1007/BF00495382

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