The invention provides a method for separating cells from
bone marrow and inducing to generate endothelial
progenitor cells, which comprises the following steps of: firstly, killing an SD (
Sprague Dawley) rat by using a cervical
vertebra dislocation method, and disinfecting the surface of the rat by using 75%
ethanol; thirdly,
cutting open the lower limbs of the rat to take out the
femur and the
tibia, and
cutting off two ends of the bone to
expose a marrow cavity; then, preparing an ECM culture medium containing 5% of fetal calf serum, 1% of ECGS and 1% of PS, and flushing the marrow cavity with the ECM culture medium until the bone becomes white; then, collecting the flushing fluid, centrifuging to remove supernate, and filtering by using a 200-mesh
cell sieve to remove impurities; then, inoculating the
cell precipitate into a six-well plate, and putting the six-well plate into a constant-temperature
incubator with the temperature of 37 DEG C and the CO2 content of 5% for culturing; after 72 hours, changing the liquid to remove non-adherent cells, and then changing the liquid once every two days until the cells need passage; and finally, when the fusion degree of the cells reaches about 80%, digesting the cells by using 0.25%
trypsin, and inoculating the cells into a T25 culture
bottle for further culture. The method is simple to operate, and the
cell purity and the differentiation efficiency of the endothelial
progenitor cells are effectively improved.