TABLE 1.
Transplanted organoids | Cell type derived | Extracellular scaffold | Receiver | Evaluation time post implantation | Blood supply | Immunosuppressive treatment | Main finding | References |
Brain organoids at 47–48 DIV | hESCs hiPSCs | Matrigel | P8–P10 CD1 mice | 2 and 4 weeks | Host brain | None | Increased cell survival and neuronal differentiation | Daviaud et al., 2018 |
Brain organoids at 40–50 DIV | hESCs | Matrigel | NOD/SCID mice | 0.5–8 months | Host brain | None | Increased neuronal differentiation and maturation; developed functional synaptic connectivity and neuronal activity between grafted and host brain | Mansour et al., 2018 |
Brain organoids at 55 DIV | hESCs | Matrigel | Sprague–Dawley rats | 4 weeks | Host brain | Cyclosporine A | Reduced cerebral infarct volume; enhance axonal regeneration and synaptic reconstruction | Wang S. N. et al., 2020 |
Brain organoids at 55 and 85 DIV | hESCs | Matrigel | Sprague–Dawley rats | 8 weeks | Host brain | Cyclosporine A | Increased neurogenesis and cell survival; improved motor function and reduced brain injury; 55-day brain organoids are better donors than that of 85-day; | Wang Z. et al., 2020 |
Brain organoids at 42 and 70 DIV | hESCs | ND | SCID mice; cynomolgus monkeys | 12 weeks | Host brain | None; tacrolimus hydrate | Extended axons along the host corticospinal tract; 42-day organoids caused graft overgrowth after transplantation | Kitahara et al., 2020 |
Brain organoids at 40–50 DIV | hESCs hiPSCs | ND | SCID mice | 1–5 months | ND | None | Increase the startle fear response of host; showing subcortical projection establishment | Dong et al., 2020 |
DIV, days in vitro; ND, not described.