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糖皮质激素和多胺参与COMMA-1D乳腺上皮细胞对锌的摄取。

Glucocorticoid and polyamine involvement in zinc uptake by COMMA-1D mammary epithelial cells.

作者信息

Allen J C, Vaillancourt S J, Haedrich L

机构信息

Department of Food Science, North Carolina State University, Raleigh 27695-7624.

出版信息

Biol Trace Elem Res. 1993 Nov-Dec;39(2-3):229-43. doi: 10.1007/BF02783193.

Abstract

The objective was to determine if a mammary cell line shows glucocorticoid stimulation of Zn uptake, and to determine whether polyamines mediate this stimulation. 65Zn uptake by COMMA-1D mouse mammary epithelial cells over a 24-h period increased significantly in cells administered 10(-7) or 10(-6) M hydrocortisone. Incorporation of 65Zn over a 1-h period was not hydrocortisone-responsive, suggesting that these incubation times represent uptake into different pools. The rate of entry into the cells over a 15-min period was significantly increased by supplementing cells with hydrocortisone with or without prolactin. Initially, cells grown in lactogenic hormone-supplemented media (10(-6) M hydrocortisone + 5 micrograms/mL ovine prolactin) had up to 65% greater 65Zn uptake over 24 h than cells in nonsupplemented growth media. 65Zn uptake from hormone media with the spermidine synthesis inhibitor methylglyoxal-bis-(guanylhydrazone) (MGBG, 10(-5)M) added was less than from growth media. Exogenous spermidine (10(-6)-10(-3)M) added to the MGBG + hormone media increased 65Zn uptake. Difluoromethylornithine (DFMO), an inhibitor of spermidine synthesis that blocks ornithine decarboxylase, caused a slight dose-dependent decrease in 65Zn uptake over the range 10(-6)-5 x 10(-3)M (p < 0.002) and tended to decrease 65Zn-uptake in lactogenic hormone-stimulated cells with 8 h of incubation, but not at other times. These data show that Zn uptake in mammary epithelial cells can be hormonally mediated by glucocorticoids and suggest that polyamines may be intracellular mediators of this effect.

摘要

目的是确定一种乳腺细胞系是否显示出糖皮质激素对锌摄取的刺激作用,并确定多胺是否介导这种刺激。在给予10(-7)或10(-6)M氢化可的松的细胞中,COMMA-1D小鼠乳腺上皮细胞在24小时内对65Zn的摄取显著增加。在1小时内65Zn的掺入对氢化可的松无反应,这表明这些孵育时间代表进入不同池的摄取。通过向细胞补充氢化可的松(无论有无催乳素),在15分钟内进入细胞的速率显著增加。最初,在补充了生乳激素的培养基(10(-6)M氢化可的松+5微克/毫升绵羊催乳素)中生长的细胞在24小时内的65Zn摄取量比未补充生长培养基的细胞高多达65%。添加了亚精胺合成抑制剂甲基乙二醛双(脒基腙)(MGBG,10(-5)M)的激素培养基中的65Zn摄取量低于生长培养基。添加到MGBG+激素培养基中的外源性亚精胺(10(-6)-10(-3)M)增加了65Zn摄取。二氟甲基鸟氨酸(DFMO)是一种阻断鸟氨酸脱羧酶的亚精胺合成抑制剂,在10(-6)-5×10(-3)M范围内导致65Zn摄取量轻微的剂量依赖性降低(p<0.002),并且在孵育8小时时倾向于降低生乳激素刺激细胞中的65Zn摄取,但在其他时间则不然。这些数据表明,乳腺上皮细胞中的锌摄取可由糖皮质激素进行激素介导,并表明多胺可能是这种作用的细胞内介质。

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