Cryopreservation of Liver-Cell Spheroids with Macromolecular Cryoprotectants

Spheroids are a powerful tool for basic research and to reduce or replace in vivo (animal) studies but are not routinely banked nor shared. Here, we report the successful cryopreservation of hepatocyte spheroids using macromolecular (polyampholyte) cryoprotectants supplemented into dimethyl sulfoxide (DMSO) solutions. We demonstrate that a polyampholyte significantly increases post-thaw recovery, minimizes membrane damage related to cryo-injury, and remains in the extracellular space making it simple to remove post-thaw. In a model toxicology challenge, the thawed spheroids matched the performance of fresh spheroids. F-actin staining showed that DMSO-only cryopreserved samples had reduced actin polymerization, which the polyampholyte rescued, potentially linked to intracellular ice formation. This work may facilitate access to off-the-shelf and ready-to-use frozen spheroids, without the need for in-house culturing. Readily accessible 3-D cell models may also reduce the number of in vivo experiments.

Automated summary

This study successfully cryopreserved hepatocyte spheroids using macromolecular cryoprotectants added to DMSO solutions, which significantly improved post-thaw recovery and minimized cryo-injury related membrane damage. Adding polyampholytes also rescued reduced actin polymerization, potentially linked to intracellular ice formation. This research may facilitate access to off-the-shelf and ready-to-use frozen spheroids, reducing the need for in-house culturing and the number of in vivo experiments.