Stem cell complex for inducing hair regeneration as well as preparation method and application of stem cell complex
A technology of stem cells and complexes, applied in the field of stem cells, can solve the problems of lack of specific cell marker molecules and low screening efficiency, and achieve the effect of avoiding complicated and cumbersome transplantation techniques, avoiding insufficient donor sites, and promoting directed differentiation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0048] Embodiment 1 Preparation and application of a stem cell complex for inducing hair regeneration, comprising the following steps:
[0049] 1) Fabrication of cell culture scaffolds
[0050] Use αMEM matrix, buffer, and acidic collagen to prepare collagen gel mixture: 100 μL ten-fold concentrated αMEM matrix, 100 μL buffer (NaOH 0.08M, HEPES 200mM), 800 μL acidic collagen solution (3mg / ml , pH3.0).
[0051] Add the above mixed solution into a sterile EP tube, use a sterile pipette tip to blow up and down to mix, use the pipette tip to suck 30-40μl and drop it on a dish or 24-well plate, and centrifuge at 300g for 10 minutes at 4°C to prevent condensation Bubbles were formed in the gel, and then the plate was incubated at 37°C for 1 hour to promote the gel to form a colloidal hanging drop.
[0052] The biomechanical range of the obtained collagen gel hanging drop: the initial elastic modulus is 13-18KPa, the maximum tensile stress is 100-500KPa, the stress relaxation time ...
Embodiment 2
[0064] Except that the steps of preparing and assembling stem cells in step 2) are different from those in Example 1, the rest of the operations are the same as in Example 1.
[0065] The steps of preparing and assembling stem cells in this example are as follows:
[0066] Recover cryopreserved HiPSCs.
[0067] First, trypsin was warmed in a 37°C water bath, and the recovered HiPSCs were washed twice with PBS, added with trypsin (0.25% trypsin: 0.4% EDTA = 1:1), and then placed at 37°C, CO 2 Incubate in an incubator with a saturated humidity of 5% for 1min, add 1-2ml of fetal bovine serum to stop trypsin, scrape the bottom of the culture plate with a pipette and blow the clones, then transfer the cell suspension to a 10ml conical centrifuge tube, Break up the colonies at the bottom of the centrifuge tube until no cell clumps are visible and a relatively homogeneous cell suspension is formed.
[0068] Centrifuge at 1400r / min for 5min, remove the supernatant, resuspend the cel...
Embodiment 3
[0075] Except step 2), all the other operations are with embodiment 2.
[0076] Prepare and assemble stem cells as follows:
[0077] After recovery from cryopreserved HiPSCs, inoculate 90 HiPSCs / 30 μl into a Nunclon round-bottom 96-well plate, add 30 μl of 15% fetal bovine serum DMEM medium to each well plate, and cultivate embryoid bodies on the third day , and continued to culture until the sixth day to obtain embryoid bodies.
[0078] Among them, in the culture medium, add TGF-β2 50ng / ml on day1; add RA1ng / ml on day2, and add RA 1ng / ml, TGF-β2 50ng / ml, EGF 20ng / ml, adenosine 30mg / ml after replacing the fresh medium on day3 , day 6 days after replacement of fresh medium, add Wint 10b 500ng / ml, Wint 3a 100ng / ml, adenosine 30mg / ml, PFI-3 2mmol / L.
[0079] Prepare siliconized-coated 35-mm Petri dishes and 1.5-mL silicone-coated test tubes, place 30 μL of collagen hanging drops on 35-mm silicone-coated tissue culture dishes, and transfer embryoid body units to In the test tube,...
PUM
Property | Measurement | Unit |
---|---|---|
Maximum tensile stress | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com