Abstract
Although primary cultures of neurons are essential methods for cell biological and pharmacological researches, many animals must be sacrificed for each experiment. Here we introduce a novel system to cryopreserve hippocampal granule cells (GCs) prepared from postnatal rats. Being thawed after as long as 60 days of cryopreservation, GCs expressed the mature neuronal marker MAP-2 and elongated single tau-1-positive axons and multiple tau-1-negative dendrites. These properties closely resembled intact GCs in primary cultures, providing the advantage of being able to repeatedly prepare stable cultures with a single sacrifice of animals. ©2007 The Japanese Pharmacological Society.
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Ichikawa, J., Yamada, R. X., Muramatsu, R., Ikegaya, Y., Matsuki, N., & Koyama, R. (2007). Cryopreservation of granule cells from the postnatal rat hippocampus. Journal of Pharmacological Sciences, 104(4), 387–391. https://doi.org/10.1254/jphs.SC0070162
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