Expandable Sendai-Virus-Reprogrammed Human iPSC-Neuronal Precursors: In Vivo Post-Grafting Safety Characterization in Rats and Adult Pig.
Yoshiomi KobayashiMichiko ShigyoOleksandr PlatoshynSilvia MarsalaTomohisa KatoNaoki TakamuraKenji YoshidaAkiyoshi KishinoMariana Bravo-HernandezStefan JuhasJana JuhasovaHana StudenovskaVladimir ProksShawn P DriscollThomas D GlennSamuel L PfaffJoseph D CiacciMartin MarsalaPublished in: Cell transplantation (2023)
One of the challenges in clinical translation of cell-replacement therapies is the definition of optimal cell generation and storage/recovery protocols which would permit a rapid preparation of cell-treatment products for patient administration. Besides, the availability of injection devices that are simple to use is critical for potential future dissemination of any spinally targeted cell-replacement therapy into general medical practice. Here, we compared the engraftment properties of established human-induced pluripotent stem cells (hiPSCs)-derived neural precursor cell (NPCs) line once cells were harvested fresh from the cell culture or previously frozen and then grafted into striata or spinal cord of the immunodeficient rat. A newly developed human spinal injection device equipped with a spinal cord pulsation-cancelation magnetic needle was also tested for its safety in an adult immunosuppressed pig. Previously frozen NPCs showed similar post-grafting survival and differentiation profile as was seen for freshly harvested cells. Testing of human injection device showed acceptable safety with no detectable surgical procedure or spinal NPCs injection-related side effects.
Keyphrases
- induced pluripotent stem cells
- spinal cord
- endothelial cells
- single cell
- ultrasound guided
- replacement therapy
- induced apoptosis
- primary care
- spinal cord injury
- oxidative stress
- neuropathic pain
- endoplasmic reticulum stress
- combination therapy
- young adults
- minimally invasive
- pluripotent stem cells
- quantum dots
- subarachnoid hemorrhage
- cord blood
- free survival
- signaling pathway