The invention relates to the technical field of
cell separation and culture, and discloses a method for separating and culturing different
cell types of musk glands of forest musk deer, which comprises the following steps of: 1, taking off the musk glands from the forest musk deer just dead of illness, simply separating glands, using one part of the musk glands for separating primary cells, and using the other part of the musk glands for separating secondary cells; one part is treated with formalin and then sent to be subjected to HE
staining slicing, and deep glands, superficial glands and sebaceous glands are distinguished; according to the method, the musk gland cells of the musk deer can serve as
primary cell strains to be stored for subsequent musk
secretion research, 0-generation cells are digested when growing to 40%-50%,
cryopreservation and passage are conducted, so that the amplification purpose is achieved, sufficient
cell strains are provided for subsequent research, and the cryopreserved 0-generation, 1-generation and 2-generation musk gland cells are stored in a
liquid nitrogen tank, so that the musk gland cells of the musk deer can be obtained. And according to the three gland cells,
mass amplification and
cryopreservation are carried out after successful separation, and the method is used for subsequent fragrance
secretion research of the fragrant gland cells.