Hair follicle reconstruction method based on hair follicle stem cells and fibroblast
A technology of hair follicle stem cells and fibroblasts, applied in medical science, prostheses, etc., can solve the problems of limiting the application of epidermal stem cells, inability to form epidermis, and easy loss of hair follicle ability, so as to achieve strong practical application prospects and scientific research potential, and avoid bacteria Pollution, reconstruction efficiency is high
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Embodiment 1
[0035] Example 1 Preparation of adult rat hair follicle stem cells
[0036] In this example, taking adult rat vibrissae hair follicle stem cells as an example, the method for preparing seed cells for hair follicle reconstruction of the present invention is described in detail, as follows. The feeding and use of experimental animals were carried out in accordance with the regulations of the Animal and Medical Ethics Committee of the Institute of Zoology, Chinese Academy of Sciences.
[0037] 1. Microdissection of rat vibrissae hair follicles
[0038] Take a small piece of adult Wistar rat (Institute of Zoology, Chinese Academy of Sciences) tentacles skin, disinfect with 75% alcohol for 3-5 minutes; under the stereoscope, use tweezers to clamp the isthmus of the tentacles hair follicles near the epidermis, and apply force toward the dermis Tear out the hair follicles; fix the hair follicles with a 29G needle, carefully scratch the dermal sheath with a scalpel, and peel off th...
Embodiment 2
[0046] Example 2 Hair follicle reconstruction based on adult rat hair follicle stem cells and newborn rat fibroblasts
[0047] 1. Preparation of fibroblasts
[0048] Pre-incubate the cell culture dish with fetal bovine serum in a 37°C incubator for 2 hours; kill the newborn rats (Experimental Animal Center, Institute of Zoology, Chinese Academy of Sciences), disinfect with 75% alcohol for 3-5 minutes, and then rinse with normal saline More than 3 times; in the ultra-clean workbench, cut the back skin with sterilized scissors; scrape off the subcutaneous fat with a scalpel; cut the skin into small pieces of 0.5cm×0.5cm; blot the serum in the culture dish, Spread the small pieces of skin evenly in the dish with the epidermis facing up. After incubating in a 37°C incubator for 2 hours, add DMEM medium containing 10% fetal bovine serum for culture; replace the culture medium every 2 days, and cultivate until needed The amount of cells was spared.
[0049] 2. Labeling of hair fol...
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