Abstracts:In order to establish an efficient tissue culture system for rapidly propagating Cunninghamia lanceolata,axillary buds from the segment were used as explants and cultured on MS medium. Effects of the different types and concentration of plant growth regulator on the germination of axillary buds and proliferation of multiple shoots were studied. The results showed that buds germination was easy using non lignified spring stem segment after broken open,and then creeping placed in culture medium. The best first medium, on which the tissue was cultured for 10 days, was MS+6-BA1.0 mg/L+NAA0.5 mg/L.Then it was transferred to the medium of MS+6-BA0.8 mg/L+NAA0.3 mg/L medium, which was the best proliferation medium and its proliferation coefficient was 4.1. Non root sterile plants could be used to cultivate excellent clones of Cunninghamia lanceolata seedlings with the traditional cutting methods.