Method for preparing tissue engineering spinal cord by using ancestral cells originated from skin
A tissue engineering spinal cord and cell technology, applied in animal cells, vertebrate cells, artificial cell constructs, etc., can solve the problem of poor repair effect, transplanted cells can not effectively play their role, neural stem cells and embryonic stem cells are difficult to achieve issues such as autologous transplantation to achieve the effect of promoting cell proliferation
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Embodiment 1
[0022] Embodiment 1 separates SKPs
[0023] After routine disinfection of the inner thigh or back skin of patients with spinal cord injury, anesthetized with 1% lidocaine, the size is about 0.5×4cm 2 full-thickness skin. Alcohol disinfection, cut the skin and put it in 0.25% trypsin to digest overnight. The next day, after washing with Hank’s solution, the epidermis and subcutaneous tissue were removed, the dermal tissue was cut into cell sheets, crushed and blown into a cell suspension, filtered and inoculated into a culture bottle containing DMEM medium. After 2 hours, the suspended cells were centrifuged and transferred to a medium suitable for the growth of SKPs (DMEM-F12, 3:1, containing 40ng / ml FGF2, 20ng / ml EGF). After culturing for about 7 days, cells growing like suspension clones could be seen SKPs, figure 1 .
[0024] Cell immunofluorescence histochemistry was used to detect whether SKPs differentiated into neurons and oligodendrocytes after induction, and the p...
Embodiment 2
[0025] Embodiment 2 SKPs rapid amplification
[0026] Usually, the growth of primary cells is relatively slow. In order to obtain a sufficient amount of cells within the optimal time window for transplantation, this example studies the promotion of proliferation of SKPs by different growth factors. According to literature research, a variety of cytokines are involved in the regulation of stem cell proliferation, mainly including basic fibroblast growth factor-2 (FGF-2), epidermal growth factor (EGF), leukemia inhibitory Factor (leukemia inhibiting factor, LIF), db-cAMP, insulin growth factor-1 (insulin growth factor-1, IGF-1), insulin growth factor-2 (insulin growth factor-2, IGF-2), platelet-derived Growth factor (Plate derived growth factor, PDGF), brain derived neurotrophic factor (brain derived neurotrophic factor, BDNF), neurotrophin-3 (neurotrophin-3, NT-3), nerve growth factor-β (nerve growth factor-β , NGF-β), bone morphogenic protein-4 (bone morphogentic protein4, BM...
Embodiment 3
[0031] Example 3 Optimization of SKPs differentiation neuron and oligodendrocyte differentiation conditions
[0032] The local microenvironment of spinal cord injury is not conducive to the differentiation of transplanted stem cells into neurons and other repair cells. Therefore, it is necessary to first explore the conditions that increase the differentiation of stem cells into neurons and other repair cells, and then combine these conditions in the tissue engineered spinal cord to improve stem cell transplantation. repair effect.
[0033] In vitro experiments were performed to observe the conditions for SKPs to differentiate into neurons and oligodendrocytes. There are three kinds of media for inducing neuron differentiation: (1) 5% FBS; (2) 6ng / ml retinoic acid; (3) 10ng / ml BDNF+10ng / ml NT3+6ng / ml retinoic acid+5%FBS. Two kinds of induction media were used for induction to Schwann cells: (1) 5% FBS; (2) 5% FBS+10 ng / ml Neuregulin. The results showed that the probability o...
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