Therapeutic agent for spinal cord injury
A technique for spinal cord injury and spinal cord, applied in the field of cell preparation of pluripotent stem cells, to achieve the effect of improving or restoring motor function
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[0081] (2) Preparation and use of cell preparations
[0082] The cell preparation of the present invention is not particularly limited, and can be obtained by suspending the Muse cells obtained in (1) above or a cell population containing Muse cells in physiological saline or an appropriate buffer (for example, phosphate-buffered saline). In this case, if the number of Muse cells isolated from autologous or allogeneic tissues is small, they can be cultured before cell transplantation until they proliferate to obtain a predetermined number of cells. In addition, as already reported (International Publication No. WO 2011 / 007900 pamphlet), Muse cells do not become tumors, so even if the cells recovered from living tissue contain an undifferentiated state, the possibility of their canceration is low. It's low, so it's safe. In addition, culture of the recovered Muse cells is not particularly limited, and can be performed in an ordinary growth medium (for example, α-minimal essent...
Embodiment 1-1
[0093] Example 1-1: Preparation of Rat Spinal Cord Injury Model
[0094] Vertebrectomy was performed on the 9th to 10th thoracic vertebrae of 11-week-old female SD rats under anesthesia to expose the spinal cord, and a weight (diameter 2.5 mm, weighing 10 grams) dropped from a height of 25mm to injure the spinal cord (3 groups, 8 rats in each group).
Embodiment 1-2
[0095] Example 1-2: Preparation of human Muse cells
[0096] Muse cells were obtained according to the method described in International Publication No. WO 2011 / 007900 concerning the isolation and identification of human Muse cells. More specifically, Muse cells are obtained by expanding enrichment culture by culturing mesenchymal stem cells under stress conditions.
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