Nomura T, Kameyama T
Cancer Lett. 1987 Jan;34(1):21-6. doi: 10.1016/0304-3835(87)90069-3.
The established cells of strain 129 mouse teratocarcinoma PCC4-aza1 were cultured in diffusion chambers inplanted into the mouse peritoneal cavities. This unique culture reduced the tumorigenic activity of PCC4-aza1 cells without changing their F9 or H-2 antigenicity in a way similar to that described previously for embryoid body cells of OTT6050 teratocarcinoma cultured in diffusion chambers. These observations suggest that a reduction in the tumorigenicity of multipotent teratocarcinoma cells is generally not accompanied by a change in expression of F9 and H-2 antigenicity.
将已建立的129品系小鼠畸胎瘤PCC4 - aza1细胞培养于植入小鼠腹腔的扩散小室中。这种独特的培养方式降低了PCC4 - aza1细胞的致瘤活性,而不改变其F9或H - 2抗原性,其方式类似于先前描述的在扩散小室中培养的OTT6050畸胎瘤的胚状体细胞。这些观察结果表明,多能性畸胎瘤细胞致瘤性的降低通常并不伴随着F9和H - 2抗原性表达的改变。