Yuan Y C, Shen S Y
Department of Hematology, Xijing Hospital, 4th Military Medical University, Xi'an.
Zhonghua Yi Xue Za Zhi. 1994 Nov;74(11):666-9, 708-9.
The promyelocytic leukemic cell line HL-60 with 20-200U/ml of low-dose rhTNF-a cultured in liquid culture system in vitro was used to observe the effect on HL-60 by TNF. TNF within dose of 50-200 U/ml can induce HL-60 cell differentiation along the monocytic-macrophage pathway, and inhibit HL-60 cell proliferation. The total RNA of HL-60 cell was used to hybrize to v-myc or v-fos probe by dot blot. We detected the expression changes of c-myc or c-fos proto-oncogene by 1-100U/ml of TNF inducing HL-60 cell for 1-12 hours. TNF could regulate the level of c-myc or c-fos mRNA, the transcription of c-myc was inhibited remarkdly, and the expression of c-fos was increased early. The results indicated that TNF in low-dose have effect on inducing HL-60 cell differentiation and regulating expression of multioncogene.
采用体外液体培养系统,用20 - 200U/ml低剂量重组人肿瘤坏死因子-α(rhTNF-α)培养早幼粒细胞白血病细胞系HL-60,观察肿瘤坏死因子(TNF)对HL-60的作用。50 - 200U/ml剂量的TNF可诱导HL-60细胞沿单核巨噬细胞途径分化,并抑制HL-60细胞增殖。用HL-60细胞的总RNA通过斑点杂交与v-myc或v-fos探针杂交。我们检测了1 - 100U/ml的TNF诱导HL-60细胞1 - 12小时后c-myc或c-fos原癌基因的表达变化。TNF可调节c-myc或c-fos mRNA水平,c-myc的转录明显受到抑制,c-fos的表达早期增加。结果表明,低剂量TNF对诱导HL-60细胞分化及调节多原癌基因表达有作用。