From: Muse cells: ushering in a new era of stem cell-based therapy for stroke
Animal | Model type | Cell type | Transplantation time/method/region/ dose | Main results | Reference |
---|---|---|---|---|---|
SCID mouse | pMCAO | Human BM-MSCs derived Muse cells | 7 days after injury onset; stereotaxical injection to ipsilateral striatum; 2.5 × 104 | Migrate and survive in the damaged site; differentiate to neurons; function recovery and tissue regeneration | [77] |
Rat | tMCAO | NHDFs-derived Muse cells | 2 days after injury onset; stereotaxical injection to ischaemic cortex; 3 × 104 | Survive up to 84 days; integrate into sensory-motor cortex; differentiate to neurons in cortex | [60] |
SCID mouse | lacunar infarction | Human BM-MSCs derived Muse cells | 2 weeks after injury onset; stereotaxical injection to perilesion site; 1 × 105 | Integrate into host brain; facilitate pyramidal tract reconstruction; differentiate to neurons; improve behaviour score; without tumour formation by 6 months | [78] |
SCID mouse | lacunar infarction | CL2020 | 9 days or 30 days after injury onset; cervical vein injection; 5 × 104/1 × 104/5 × 103 | Survive in host brain for at least 22 weeks; without tumorigenesis; differentiate to neurons; behaviour improvement | [79] |
SCID mouse | ICH | Human BM-MSCs derived Muse cells | 5 days after injury onset; stereotaxical injection to hematoma cavity; 2 × 105 | Improve motor function recovery; differentiate to neurons; much higher survival rate of Muse cells compared with non-Muse cells | [80] |