Objective: To study the effective method of isolation, culture and proliferation of rat bone marrow-derived dendritic cells (DC) in vitro.

目的：探讨体外分离、培养和扩增大鼠骨髓来源树突状细胞(DC)的有效方法。

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Dendritic cells (DC) are bone marrow-derived professional antigen-presenting cells.

树突状细胞(DC)是骨髓来源的专职抗原呈递细胞。

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The mouse bone marrow, derived dendritic cells(DC) were pulsed with HTA, HSP70BCG or HTA, HSP70BCG, and their antigen capturing and antigen presenting capacities were evaluated.

利用HTA、HSP70BCG、HTA-HSP70BCG体外冲激小鼠骨髓树突状细胞，观察树突状细胞的抗原捕获能力及抗原提呈能力的变化。

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The mouse bone marrow, derived dendritic cells(DC) were pulsed with HTA, HSP70BCG or HTA, HSP70BCG, and their antigen capturing and antigen presenting capacities were evaluated.

利用HTA、HSP70BCG、HTA-HSP70BCG体外冲激小鼠骨髓树突状细胞，观察树突状细胞的抗原捕获能力及抗原提呈能力的变化。

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