Composition capable of inducing stem cells to secrete cytokines and its application
A technology of cytokines and mesenchymal stem cells, applied in the field of compositions capable of inducing stem cells to secrete cytokines, can solve problems such as undisclosed induction compositions, and achieve the effects of avoiding social and ethical disputes, low immune rejection, and fast proliferation
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Embodiment 1
[0034] This embodiment provides a composition capable of inducing stem cells to secrete cytokines and its application. Specifically, the composition is added to high-sugar DMEM to prepare a culture medium for inducing umbilical cord mesenchymal stem cells to secrete cytokines, and to stimulate umbilical cord mesenchymal stem cells to secrete cytokines.
[0035] 1. Medium for inducing umbilical cord mesenchymal stem cells to secrete cytokines (see Table 1): 100 mL of high-sugar DMEM, 3 mg of VA, 75 mg of glutamine, 1 mg of lysophosphatidic acid, and 0.05 mg of icariin.
[0036] 2. The method of inducing umbilical cord mesenchymal stem cells to secrete cytokines:
[0037] (1) Take the umbilical cord mesenchymal stem cells, culture them in the umbilical cord mesenchymal stem cell medium, and when the cells grow to about 85%, continue to subculture in the umbilical cord mesenchymal stem cell medium;
[0038] (2) Transfer the P3-P5 cells to the mechanical stretching cell culture b...
Embodiment 2
[0043] This embodiment is a modification example of Embodiment 1, and the changes relative to Embodiment 1 include:
[0044] 1. Medium for inducing umbilical cord mesenchymal stem cells to secrete cytokines (see Table 1): 100 mL high-glucose DMEM, 1 mg VA, 50 mg glutamine, 0.5 mg lysophosphatidic acid, and 0.01 mg icariin.
[0045] 2. In step (2): Transfer P3-P5 cells to the mechanically stretched cell culture box. When the cell growth density reaches 50%-65%, discard the original umbilical cord mesenchymal stem cell culture medium and wash with PBS for three times. Replace with the culture medium that induces umbilical cord mesenchymal stem cells to secrete cytokines. After culturing for 1 hour, stretch the elastic membrane by 5% every 10 hours according to the scale on the wall of the mechanical pulling culture box, and place it in a carbon dioxide incubator. Cultivation was continued for 24 hours; other operations were the same as in Example 1.
Embodiment 3
[0047] This embodiment is a modification example of Embodiment 1, and the changes relative to Embodiment 1 include:
[0048] 1. Medium for inducing umbilical cord mesenchymal stem cells to secrete cytokines (see Table 1): 100 mL of high-sugar DMEM, 5 mg of VA, 100 mg of glutamine, 2 mg of lysophosphatidic acid, and 0.1 mg of icariin.
[0049] 2. In step (2): Transfer P3-P5 cells to the mechanically stretched cell culture box. When the cell growth density reaches 50%-65%, discard the original umbilical cord mesenchymal stem cell culture medium and wash with PBS for three times. Replace with the medium that induces umbilical cord mesenchymal stem cells to secrete cytokines for culture. After 3 hours of culture, stretch the elastic membrane by 15% every 15 hours according to the scale on the wall of the mechanical pulling culture box, and place it in a carbon dioxide incubator. Cultivation was continued for 48 hours; other operations were the same as in Example 1.
[0050] Table...
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