Umbilical cord mesenchymal stem cell modified by Nrf2 gene as well as preparation method and application thereof
A technology of mesenchymal stem cells and gene modification, applied in the field of stem cells
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Embodiment 1
[0063] The construction of embodiment one recombinant plasmid
[0064] 1. Collect 2ml of peripheral anticoagulant blood from 16 normal healthy people (28.3±10.5 years old), and mix all the blood evenly. Take 2ml of well-mixed peripheral blood, add 12ml of erythrocyte lysate within 4h, centrifuge at 1000rpm for 5min, discard the supernatant, resuspend and wash with PBS, add 1ml of Trizol lysate, and extract RNA. According to Takara RT Master Mix reverse transcription kit operating instructions, take 500ng of total RNA for reverse transcription, the reaction system is 1μl, the reaction conditions are 37°C for 15min, 85°C for 15s, and the reaction product is stored at -20°C for future use. The reaction system is as follows:
[0065] Template RNA 1μl
[0066] RT enzyme Master Mix 2μl
[0067] DEPC ddH 2 O 7μl
[0068] 2. Use primers Forward: 5'-cgcggatccgcgatggatttgat-3', Reverse: 5'-cgacgcgtcgagaaaaactag-3', and use the cDNA obtained in step 1 as a template for conventiona...
Embodiment 2
[0072] Example 2 Acquisition of Nrf2 Gene Modified Umbilical Cord Mesenchymal Stem Cells
[0073] 1. Take 5×10 293T cells in the logarithmic growth phase 6 Inoculate each in a 100mm cell culture dish. After 24 hours, when the cell confluence reaches 80%-90%, replace it with 6ml of fresh DMEM complete medium. After 4 hours, add 0.5ml of the target plasmid pWPXL-Nrf210μg, packaging plasmid pMD2.G 6.5 μg and envelope plasmid psPAX2 3.5μg mixture, and slowly add 50μl CaCl 2 , mixed gently, used for lentivirus packaging. The virus liquid after packaging for 48h and 72h was collected, concentrated and stored at -80°C for later use.
[0074] 2. Collect discarded umbilical cord tissue from the hospital, transfer the umbilical cord tissue to a sterile collection bottle, store it at 2-8°C, and separate Wharton's jelly within 12 hours. Separated Wharton's jelly with hMSC SFM culture medium adherent culture in T75 culture flask, placed at 37 degrees Celsius, 5% CO 2 cultured in an i...
Embodiment 3
[0078] Example 3 UCMSC-Nrf2 against nerve cell damage
[0079] When cells are damaged or die, intracellular lactate dehydrogenase (lactate dehydrogenase, LDH) will be released into the cell culture medium, so LDH is an important indicator for detecting cell damage or death. The hydrogen peroxide model of nerve cell PC12 and the Aβ25-35 model were used as nerve cell injury models. Take the nerve cell PC12 to 1×10 5 The density of / hole is inoculated in 6 hole plate, and adds the UCMSC (1 * 10 4 / hole). After 24 hours of culture, the cells were divided into A: control group, B: hydrogen peroxide group, C: UCMSC+H 2 o 2 Panel, D: UCMSC-Nrf2+H 2 o 2 Group, E: Aβ25-35 group, F: UCMSC+Aβ 25-35 Group, G: UCMSC-Nrf2+Aβ25-35 group. Add H to the holes corresponding to the group 2 o 2 and Aβ25-35, so that their final concentrations were 200 μM and 20 μM, respectively. After co-incubating for 12 hours, the cell supernatant was collected, and LDH was detected according to the in...
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