Method for enhancing efficacy of stem cells by using ethionamide
A technology of ethionamide and stem cells, which is applied in the field of medium compositions for enhancing stem cell efficacy, can solve problems such as insufficient development, prevent or treat inflammatory diseases or degenerative brain diseases, and improve anti-inflammatory effects. , anti-inflammatory effect improvement effect
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Embodiment 1
[0082] Example 1. Preparation of human umbilical with metamorite stem cells
[0083] After obtaining the umbilical cord after approved by IRB (IRB # 2015-09-023-003) according to Samsung Medical Center, the human umbilical-cord serum is separated by the following method.
[0084] First, a 3 to 4 cm of umbilical cord tissue was combined, and the collagen enzyme solution (GIBCO, USA) was treated with an extracellular matrix, and then 0.25% trypsin (GIBCO, USA) was digested at 37 ° C for 30 minutes. . Subsequently, the cells were obtained by adding a fetal bovine serum (FBS) (Biowest, USA) to the resulting product, then centrifuged at 1000 × g for 10 minutes, then use 10% FBS and 50μg / ml to celebrate MEM medium (Minimum Essential Media) (GIBCO, USA) (GIBCO, USA) (GIBCO, USA) at 37 ° C, 5% CO 2 The environment is cultured, thereby passing between 5 or 6 mesenchymal stem cells being used in experiments.
Embodiment 2
[0085] Example 2. Preparation of human umbilical-tape mesenchymal stem cells passing through vs.
[0086] 6 × 10 3 Cell / cm 2 The human umbilical binding mesenchymal stem cells prepared according to Example 1 were treated in a cell culture vessel while 50 μm, 100 μm or 150 μm concentrations were treated with ethylene isoparamia, and then cultured for 72 hours.
Embodiment 3
[0087] Example 3. Verification of stem cell anti-inflammation effect
[0088] In order to demonstrate whether the anti-inflammatory effect of stem cells is improved when treating mesenchymal stem cells with ethylene isoparamia, and performs the following experiments. Specifically, the inflammatory model is to induce inflammatory model by treating microglia Bv2 cells with LPS (lipopolysaccharide, LipopolysAccharide), and is also mixed with EtOAc. Coute, subsequently measured nitric oxide; NO), NO-related factor and the expression level of the active oxygen.
[0089] As a result, if Figure 1A As shown in the case of representative NO-related inflammatory factors, INOS (induced nitric oxide synthase, inducible nitric oxide synthase), metallic stem cells with control or with ethylene Compared with the co-cultured group, mRNA expression was significantly reduced in groups of methatetransfeitrous stem cells with vs. In addition, if Figure 1B and 1c As shown, according to the results of...
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