Inducer for inducing human adipose derived stromal cells into insulin-secretion cells, induction medium and method
A technology of insulin secretion and induction medium, applied in the field of biomedicine, can solve the problems of complicated induction process, long induction time, and small number of cells, and achieve the effect of broad clinical application prospects, no ethical problems, and high differentiation efficiency
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Embodiment 1
[0028] Example 1 The inducer for inducing human adipose-derived mesenchymal stem cells into insulin-secreting cells in this example is composed of the following components in mass concentration ratio: Dazhu Rhodiola injection 20 g / L, nicotinamide 1.2g / L, taurine 0.50 g / L, GLP-1 30.5 mg / L.
[0029] The composition ratio of the induction medium containing the above-mentioned inducer is as follows: in each 1000ml of the induction medium, 20 g of Dazhu Rhodiola injection, 1.2 g of nicotinamide, 0.5 g of taurine, 30.5 mg of GLP-1, and the remaining The amount is human mesenchymal stem cell serum-free medium, and the above-mentioned components are mixed and then filtered and sterilized to prepare the inducer medium of the present invention.
[0030] The components of the inducer and induction medium of the present invention are all commercially available products: human mesenchymal stem cell serum-free medium, LONZA, 00190632; Dazhu Rhodiola injection, Tonghua Yusheng Pharmaceutica...
Embodiment 2
[0031] Example 2 This example is a method for inducing human adipose-derived mesenchymal stem cells into insulin-secreting cells, including the following steps:
[0032] 1. Preparation of adipose-derived mesenchymal stem cells:
[0033] 1. To receive adipose tissue, wipe the outer wall of the container containing adipose tissue with 75% alcohol.
[0034] 2. Dispense adipose tissue, each T175 culture bottle is divided into 50ml adipose tissue. With a 10ml pipette, remove the tip, first absorb the lower layer of red liquid in the fat collection bottle and discard it, and mix the remaining upper layer of fat before subpackaging.
[0035] 3. Wash fat tissue and remove blood cells. Add 100ml of sodium chloride injection to the T175 culture flask, tighten the cap, shake vigorously for 3 minutes to fully wash the adipose tissue, then stand still for 3-5 minutes to separate the different phases, and suck off the lower aqueous phase; repeat the above operation three times until The ...
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