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bioRxiv · 10.64898/2026.01.28.702375

Ultrastructural and Histological Cryopreservation of Mammalian Brains by Vitrification

FAHY, G. M.·Spindler, R. M.·Wowk, B. G.·Vargas, V. M.·La, R.·Thomson, B.·Roa, R.·Hugh, H.·Graber, S.·Ge, X.·Sharif, A.·Harris, S. B.·Coles, L. S.
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Abstract

Studies of whole brain cryopreservation are rare but are potentially important for a variety of applications. It has been demonstrated that ultrastructure in whole rabbit and pig brains can be cryopreserved by vitrification (ice-free cryopreservation) after prior aldehyde fixation, but fixation limits the range of studies that can be done by neurobiologists, including studies that depend upon general molecular integrity, signal transduction, macromolecular synthesis, and other physiological processes. We now show that whole brain ultrastructure can be preserved by vitrification without prior aldehyde fixation. Rabbit brain perfusion with the M22 vitrification solution followed by vitrification, warming, and fixation showed an absence of visible ice damage and overall structural preservation, but osmotic brain shrinkage sufficient to distort and obscure neuroanatomical detail. Neuroanatomical preservation in the presence of M22 was also investigated in human cerebral cortical biopsies taken after whole brain perfusion with M22. These biopsies did not form ice upon cooling or warming, and high power electron microscopy showed dehydrated and electron-dense but predominantly intact cells, neuropil, and synapses with no signs of ice crystal damage, and partial dilution of these samples restored normal cortical pyramidal cell shapes. To further evaluate ultrastructural preservation within the severely dehydrated brain, rabbit brains were perfused with M22 and then partially washed free of M22 before fixation. Perfusion dilution of the brain to 3-5M M22 resulted in brain re-expansion and the re-appearance of well-defined neuroanatomical features, but rehydration of the brain to 1M M22 resulted in ultrastructural damage suggestive of preventable osmotic injury caused by incomplete removal of M22. We conclude that both animal and human brains can be cryopreserved by vitrification with predominant retention of ultrastructural integrity without the need for prior aldehyde fixation. This observation has direct relevance to the feasibility of human cryopreservation, for which direct evidence has been lacking until this report. It also provides a starting point for perfecting brain cryopreservation, which may be necessary for lengthy space travel and could allow future medical time travel.

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FAHY, G. M., Spindler, R. M., Wowk, B. G., Vargas, V. M., La, R., Thomson, B., Roa, R., Hugh, H., Graber, S., Ge, X., Sharif, A., Harris, S. B., Coles, L. S.. 2026-02-01. Ultrastructural and Histological Cryopreservation of Mammalian Brains by Vitrification. https://doi.org/10.64898/2026.01.28.702375

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