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甲状腺激素对大鼠肝癌细胞系中Na(+)-K(+)-ATP酶及其mRNA的诱导作用

Thyroid hormone induction of Na(+)-K(+)-ATPase and its mRNAs in a rat liver cell line.

作者信息

Gick G G, Ismail-Beigi F

机构信息

Department of Biochemistry, Columbia University, College of Physicians and Surgeons, New York, New York 10032.

出版信息

Am J Physiol. 1990 Mar;258(3 Pt 1):C544-51. doi: 10.1152/ajpcell.1990.258.3.C544.

Abstract

The expression of mRNAs encoding the alpha- and beta-subunits of Na(+)-K(+)-ATPase (Na(+)-K+ pump) was examined in a rat liver cell line, Clone 9, in various thyroidal states. Northern blot analysis of total RNA isolated from cells incubated in hypothyroid serum-containing medium revealed the expression of mRNAs encoding Na(+)-K(+)-ATPase alpha 1-(mRNA alpha 1) and beta- (mRNA beta) subunits; mRNAs encoding the alpha 2- and alpha 3-subunits were undetectable. There was a discrepancy in the abundance of mRNA alpha 1 relative to mRNA beta such that mRNA alpha 1 exceeded the sum of the multiple mRNA beta bands by approximately 35-fold. 3,3',5-Triiodothyronine (T3) produced a coordinate augmentation of mRNA alpha 1 and mRNA beta contents that was demonstrable within 2 h and preceded the stimulation of Na(+)-K(+)-ATPase activity. After incubation of cells with T3 for 48 h, Na(+)-K(+)-ATPase activity was stimulated by 1.32-fold, whereas mRNA alpha 1 and mRNA beta abundances were increased 1.46- and 2.87-fold, respectively. Treatment of cells for 6 h with 10 micrograms/ml cycloheximide, a concentration sufficient to inhibit protein synthesis by 95%, elicited a 3.5- and 5.1-fold increase in mRNA alpha 1 and mRNA beta content, respectively. Cycloheximide abrogated the stimulatory effect of T3 on mRNA beta abundance, whereas the T3-induced increase in mRNA alpha 1 content was not prevented.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在不同甲状腺状态下,对大鼠肝细胞系克隆9中编码钠钾ATP酶(钠钾泵)α和β亚基的mRNA表达进行了检测。对在含甲状腺功能减退血清的培养基中培养的细胞分离得到的总RNA进行Northern印迹分析,结果显示编码钠钾ATP酶α1亚基(mRNAα1)和β亚基(mRNAβ)的mRNA有表达;未检测到编码α2和α3亚基的mRNA。mRNAα1相对于mRNAβ的丰度存在差异,mRNAα1比多个mRNAβ条带的总和高出约35倍。三碘甲状腺原氨酸(T3)使mRNAα1和mRNAβ含量协同增加,在2小时内即可显现,且先于钠钾ATP酶活性的刺激。细胞用T3孵育48小时后,钠钾ATP酶活性提高了1.32倍,而mRNAα1和mRNAβ的丰度分别增加了1.46倍和2.87倍。用10微克/毫升环己酰亚胺处理细胞6小时,该浓度足以抑制蛋白质合成95%,结果分别使mRNAα1和mRNAβ含量增加了3.5倍和5.1倍。环己酰亚胺消除了T3对mRNAβ丰度的刺激作用,而T3诱导的mRNAα1含量增加并未被阻止。(摘要截断于250字)

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