Ohara T, Ikeda U, Muto S, Oguchi A, Tsuruya Y, Yamamoto K, Kawakami K, Shimada K, Asano Y
Department of Nephrology, Jichi Medical School, Tochigi, Japan.
Am J Physiol. 1993 Sep;265(3 Pt 2):F370-6. doi: 10.1152/ajprenal.1993.265.3.F370.
Thyroid hormone 3,3',5-triiodothyronine (T3) is an important regulator of Na(+)-K(+)-adenosinetriphosphatase (Na(+)-K(+)-ATPase) activity in a variety of mammalian target tissues. In the present study, we examined the expression of Na(+)-K(+)-ATPase alpha- and beta-subunit mRNAs by T3 in cultured rat mesangial cells. Northern blot analysis of total RNA isolated from cultured rat mesangial cells revealed the expression of mRNAs encoding Na(+)-K(+)-ATPase alpha 1- and beta 1-subunits; mRNAs encoding alpha 2- and alpha 3-subunits were undetectable. Exposure of mesangial cells to T3 (10(-8) M) caused a threefold increase in the alpha 1-mRNA expression, which was first detected at 6 h and sustained for at least 48 h. The beta 1-mRNA expression was gradually increased by T3, with a maximum fourfold elevation at 48 h. The 50% effective concentration (EC50) for the alpha 1- and beta 1-mRNA induction by T3 was approximately 10(-10) M. The half-life of alpha 1-mRNA analyzed by actinomycin D chase was approximately 3 h and was not affected by T3. The augmented alpha 1-mRNA expression by T3 was associated with a 2.4-fold increase in the alpha 1-subunit protein accumulation and a 1.6-fold increase in Na(+)-K(+)-ATPase activity. These data suggest that thyroid hormone stimulates Na(+)-K(+)-ATPase gene expression, protein accumulation, and enzyme activity in rat mesangial cells.
甲状腺激素3,3',5-三碘甲状腺原氨酸(T3)是多种哺乳动物靶组织中钠钾ATP酶(Na(+)-K(+)-ATPase)活性的重要调节因子。在本研究中,我们检测了T3对培养的大鼠系膜细胞中钠钾ATP酶α和β亚基mRNA表达的影响。对培养的大鼠系膜细胞分离的总RNA进行Northern印迹分析,结果显示了编码钠钾ATP酶α1和β1亚基的mRNA的表达;未检测到编码α2和α3亚基的mRNA。将系膜细胞暴露于T3(10(-8) M)导致α1-mRNA表达增加了三倍,在6小时时首次检测到,并持续至少48小时。T3使β1-mRNA表达逐渐增加,在48小时时最大升高四倍。T3诱导α1和β1-mRNA的50%有效浓度(EC50)约为10(-10) M。用放线菌素D追踪分析α1-mRNA的半衰期约为3小时,且不受T3影响。T3增强的α1-mRNA表达与α1亚基蛋白积累增加2.4倍和钠钾ATP酶活性增加1.6倍相关。这些数据表明甲状腺激素刺激大鼠系膜细胞中钠钾ATP酶基因表达、蛋白积累和酶活性。