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野生型和冷敏感E1a突变型5型腺病毒转化的CREF细胞中钠钾ATP酶的甲状腺诱导性调节及表皮生长因子的结合

Regulation of thyroidal inducibility of Na,K-ATPase and binding of epidermal growth factor in wild-type and cold-sensitive E1a mutant type 5 adenovirus-transformed CREF cells.

作者信息

Guernsey D L, Duigou G J, Babiss L E, Fisher P B

机构信息

Department of Physiology and Biophysics, University of Iowa College of Medicine, Iowa City 52242.

出版信息

J Cell Physiol. 1987 Dec;133(3):507-14. doi: 10.1002/jcp.1041330311.

Abstract

We have analyzed the relationship between expression of the transformed phenotype and thyroid hormone (triiodothyronine, T3) inducibility of Na,K-ATPase and binding of 125I-epidermal growth factor (EGF) to cell membrane receptors in wild-type (wt) and mutant type 5 adenovirus (Ad5)-transformed CREF cells displaying a cold-sensitive (cs) expression of the transformed phenotype. CREF cells respond to thyroid hormone treatment with increased Na,K-ATPase activity and bind similar levels of 125I-EGF at 32 degrees C, 37 degrees C and 39.5 degrees C. In contrast, CREF cells transformed by wt Ad5 or the E1a plus E1b-transforming genes of wt Ad5 are refractile to T3 treatment and bind lower levels of 125I-EGF than CREF cells at all three temperatures. By employing a series of cloned CREF cell lines transformed by a host-range cold-sensitive mutant virus, H5hr1 or H5dl101, or the E1a or E1a plus E1b genes from these viruses, we have investigated expression of the transformed state and its relationship with hormone inducibility and EGF binding. When cs virus, cs E1a- or cs E1a plus E1b-transformed CREF clones were grown at 32 degrees C, a nonpermissive transforming temperature in which cs-transformed cells exhibit properties similar to untransformed CREF cells, T3 induced Na,K-ATPase activity and these cells bound similar levels of 125I-EGF as CREF cells. However, when cs virus- and cs Ela plus E1b-transformed CREF clones were incubated at 37 degrees C or 39.5 degrees C, temperatures at which cs-transformed cells exhibit properties similar to wt Ad5-transformed CREF cells, they did not respond to T3 and bound lower levels of 125I-EGF than CREF cells. In the case of cs E1a-transformed CREF clones, thyroid hormone responsiveness was observed at both 32 degrees C and 37 degrees C, but not at 39.5 degrees C. By performing temperature shift experiments--i.e. 32 degrees C to 37 degrees C, 32 degrees C to 39.5 degrees C, 37 degrees C to 32 degrees C, and 39.5 degrees C to 32 degrees C, it was demonstrated that after a shift from lower to higher temperature a 24-hr lag period was required for cs-transformed CREF cells to lose T3 inducibility and exhibit reduced EGF binding, whereas 96 hr after a shift from higher to lower temperature a 96-hr lag period was required for cs-transformed cells to regain T3 inducibility and increased 125I-EGF binding.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

我们分析了野生型(wt)和5型突变腺病毒(Ad5)转化的CREF细胞中转化表型的表达与甲状腺激素(三碘甲状腺原氨酸,T3)诱导的Na,K - ATP酶活性以及125I - 表皮生长因子(EGF)与细胞膜受体结合之间的关系,这些细胞呈现出转化表型的冷敏感(cs)表达。CREF细胞在32℃、37℃和39.5℃下对甲状腺激素处理的反应是Na,K - ATP酶活性增加,并且结合相似水平的125I - EGF。相比之下,由wt Ad5或wt Ad5的E1a加E1b转化基因转化的CREF细胞对T3处理无反应,并且在所有三个温度下结合的125I - EGF水平均低于CREF细胞。通过使用一系列由宿主范围冷敏感突变病毒H5hr1或H5dl101或这些病毒的E1a或E1a加E1b基因转化的克隆CREF细胞系,我们研究了转化状态的表达及其与激素诱导性和EGF结合的关系。当cs病毒、cs E1a或cs E1a加E1b转化的CREF克隆在32℃生长时,这是一个非允许转化温度,在此温度下cs转化细胞表现出与未转化CREF细胞相似的特性,T3诱导Na,K - ATP酶活性,并且这些细胞结合的125I - EGF水平与CREF细胞相似。然而,当cs病毒和cs Ela加E1b转化的CREF克隆在37℃或39.5℃孵育时,在这些温度下cs转化细胞表现出与wt Ad5转化的CREF细胞相似的特性,它们对T3无反应,并且结合的125I - EGF水平低于CREF细胞。对于cs E1a转化的CREF克隆,在32℃和37℃均观察到甲状腺激素反应性,但在39.5℃未观察到。通过进行温度转换实验,即从32℃到37℃、从32℃到39.5℃、从37℃到32℃以及从39.5℃到32℃,结果表明,从较低温度转换到较高温度后,cs转化的CREF细胞需要24小时的延迟期才能失去T3诱导性并表现出EGF结合减少,而从较高温度转换到较低温度96小时后,cs转化细胞需要96小时的延迟期才能恢复T3诱导性并增加125I - EGF结合。(摘要截断于400字)

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