You are hereMay 3, 2019
New ultra-rapid cooling process promises to transform cell-freezing practice
MATSUMOTO (JP), April 2019 — A team of Japanese researchers has for the first time demonstrated how to preserve frozen animal cells without a cryoprotectant agent (CPA), a substance that can protect biological material from freezing damage. To keep cells alive, all the conventional freezing methods needed to add a CPA, which can be potentially toxic and associated with cell damage and death.
This new method relies on ultra-rapid cooling — or really fast freezing — that keeps cells and vital biological material during freezing process. A safe freezing without CPA would not only revolutionize how important research and medical material is stored, but greatly advance any and all research methods within those fields.
The study was published recently in Proceedings of the National Academy of Sciences (PNAS).
The aim of cryopreservation — or storing in low temperatures — is to maintain biological materials, including tissues, mammalian cells, bacteria, fungi, plant cells and viruses. These also include stem cells, sperm and embryos, all of which may subsequently be used for research and/or clinical purposes.
When performed correctly and taking into account cell and tissue specific criteria, cryopreservation is an effective means for continuous and long-term storage and availability of tissues and genetically stable living cells for academic, industrial and clinical research. In order to keep frozen cells alive, the water inside and outside of those cells must be vitrified or turned into really small crystal structures. So far, this has been achieved only by adding at least one CPA to the medium.
For this study, the researchers were able to freeze the cells quickly and achieved vitrification similarly to the use of CPA.
"Ultra-rapid cooling is much faster than the cooling rate that is typically used in cryopreservation. We call it ‘super-flash’ freezing, and it can almost vitrify and cryopreserve living cells without any cryoprotectant agent," said Yoshitake Akiyama, Ph.D., corresponding author and associate professor in the Department of Mechanical Engineering and Robotics at Shinshu University.
The critical cooling rate required for CPA-free ultra-rapid freezing is 10,000 degrees C per second, and the researchers, in order to achieve it, used the inkjet cell printing technology. With this inventive approach, they repeatedly experimented how they could minimize the object of freezing and finally found that super-flash freezing was realized with droplet sizes below 40 picoliter.
The researchers tested their CPA-free procedure by ultra-rapid cooling one kind of mouse cells and obtained results that are very comparable to freezing with CPA. The method was further confirmed on a different mouse cell line and rat mesenchymal stem cells, thereby demonstrating both efficacy as well as broad applicability.
In the future, the researchers hope to apply their method to preserve various types of cells, including those that have been particularly sensitive to the cryopreservation procedure.
"We plan to use our method to cryopreserve other cells including pluripotent stem cells, whose properties such as stemness and differentiation are known to be susceptible to CPAs. Furthermore, we believe that our method might be suitable for cells such as hemocytes that cannot be stored by a conventional cryopreservation method," Professor Akiyama added.
Inkjet-printed droplet array frozen by liquid nitrogen on a thin glass. Image courtesy of © 2019 National Academy of Sciences.