A kind of layered co-cultivation method of mammalian intramuscular adipocytes and skeletal muscle cells
A technique for intramuscular fat cells and skeletal muscle cells, applied in the field of cell biology, can solve the problems of difficult separation of pre-adipocytes and many miscellaneous cells, and achieve the effects of saving test costs, simple technology and few steps.
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[0044] Meat quality is mainly determined by muscle cell type and intramuscular fat content. The 3T3‐L1 preadipocyte cell line and the primary cultured adipose stromal microtubule cells (SVF) of various animals are the main cell models for studying the proliferation and differentiation of adipocytes. However, these cell models have their own disadvantages: for example, the 3T3-L1 cell line is derived from 17-19 day-old mouse embryo cells, and its chromosomes are aneuploid, which cannot reflect the animal environment well; although the primary cultured SVF can better The simulated animal in vivo environment, but the purity of this kind of cells is not high, which is not conducive to fine research. In view of the above problems, people are looking for a preadipocyte model that can more accurately reflect the differentiation process of intramuscular adipocytes. Skeletal muscle accounts for 40%-50% of animal body weight and is an important animal product. The establishment of skel...
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