The invention discloses a renal tubular epithelial
cell separation and culture method which comprises the following steps: S1, mechanical tissue separation: taking a
renal tissue sample, separating a cortex part, and then
cutting into pieces; s2, enzymolysis: digesting with a mixed
enzyme, and centrifuging; and S3,
cell culture: resuspending the
cell precipitate by using a complete culture medium, and inoculating the cell precipitate into a culture
bottle. Wherein mechanical separation is simple, and mechanical damage is reduced to the maximum extent. The best
digestion efficiency is achieved through mild enzymolysis, the obtained cells are high in activity, the activity of the obtained cells can reach 50% or above, the number of the cells at least reaches 1 * 10 < 6 > / g, the cells have high proliferation performance and high initial
inoculation density, the cell proliferation environment pressure is small, a simple and convenient
nutrient medium rich in
nutrition is added, substrate layer planking is not needed, and the cost is low. The cell proliferation speed is at least one time faster than that reported in the literature; and if 1 * 10<6> cells are inoculated in a T75
bottle, complete convergence can be achieved within 72 hours.