Muscle-derived cell blood glucose response type expression SIA promoter, recombinant vector and construction method and application thereof
A recombinant vector and construction method technology, applied in the field of biomedicine, can solve the problems of short cell life cycle and cannot achieve long-term therapeutic effect, and achieve the effects of avoiding hypoglycemia side effects, simple construction method and convenient operation.
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Embodiment 1
[0040] The present invention will be further described below in conjunction with the accompanying drawings and examples. The protection scope of the present invention is not limited to the following: Example 1: pGREMS promoter cell specificity experiment
[0041] 1. Preparation of Reagents
[0042] C2C12 mouse myoblasts, 293T human embryonickidney cells, HEK-293 human embryonic kidney cells (Human Embryonic Kidney 293), NIH3T3 mouse embryo fibroblast cell All were purchased from the Cell Resource Center, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences. The reagent formulations used are shown in Table 1.
[0043] Table 1 Reagent formula
[0044]
[0045] 2. Construction of the plasmid
[0046] A blood glucose-responsive enhanced muscle-specific promoter pGREMS was designed, and the pGREMS sequence was cloned by overlapping PCR and cloned into the pSC plasmid, and the sequence was checked to ensure that the sequence was completely accurate. Plasmi...
Embodiment 2
[0067] Example 2: SIA plasmid in vivo experiment
[0068] C57BL / 6J male mice, purchased at 6 weeks old, were adaptively fed for 1 week. Establishment of type 1 diabetes mouse model: The model mice were injected with STZ solution (60 mg / kg) on an empty stomach for 5 consecutive days. For injection, STZ was dissolved in citrate buffer (pH 4.5) and prepared on ice protected from light. After the injection, fast for 6 hours. From the third day after the injection, the blood of the mice was collected by the tail clipping method, the tail tip was cut off by 1-2 mm, the first drop was discarded, and the blood glucose was detected with a Roche blood glucose meter. It was considered that the diabetes model was constructed successfully.
[0069] The successfully modeled mice were randomly divided into groups: T1D group (modeling, no treatment), Exp1 group (modeling, injected with pGREMS-SIA3), Exp2 group (modeling, injected with pGREMS-SIA4) and Exp3 group ( Modeling, injection of...
Embodiment 3
[0090] Example 3: Detection of oxidative stress markers
[0091] 1 Detection of reduced glutathione (GSH) content in kidney and serum of mice
[0092] GSH detection According to the instructions of the Solebao reduced glutathione (GSH) content detection kit (Cat: BC1175) operation 2 Malondialdehyde (MDA) content detection
[0093] MDA detection was performed according to the instructions of Solebao Malondialdehyde (MDA) Content Detection Kit (Cat: BC0025) 3 Superoxide dismutase (SOD) activity detection
[0094] SOD detection was performed according to the instructions of Solebao Superoxide Dismutase (SOD) Activity Detection Kit (Cat: BC0175) 4 Total Antioxidant Capacity (T-AOC) Detection
[0095] The T-AOC test was performed in accordance with the instructions of the Solebao Total Antioxidant Capacity (T-AOC) Test Kit (Cat: BC1315)
[0096] The contents of four oxidative stress markers GSH, T-AOC, MDA and SOD in serum and kidney of mice in each group were detected 60 days af...
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