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8-氯-cAMP诱导cAMP依赖性蛋白激酶的RIα亚基截短和下调以及RIIβ亚基上调,导致II型全酶依赖性生长抑制和HL-60白血病细胞分化。

8-Cl-cAMP induces truncation and down-regulation of the RI alpha subunit and up-regulation of the RII beta subunit of cAMP-dependent protein kinase leading to type II holoenzyme-dependent growth inhibition and differentiation of HL-60 leukemia cells.

作者信息

Rohlff C, Clair T, Cho-Chung Y S

机构信息

Cellular Biochemistry Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Biol Chem. 1993 Mar 15;268(8):5774-82.

PMID:8449943
Abstract

8-Cl-cAMP, a site-selective cAMP analog, induces growth inhibition in a variety of cell types of human cancer cell lines. This inhibitory effect of 8-Cl-cAMP was related to its ability to differentially regulate type I versus type II cAMP-dependent protein kinase. In the present study we demonstrated a unique mechanism of action of 8-Cl-cAMP in the regulation of these kinase isozymes in HL-60 human promyelocytic leukemia cells. High-performance liquid chromatography (HPLC) resolved various isoforms of protein kinase present in HL-60 cells. In control cells, type I protein kinase (PKI) comprised more than 90% and type II protein kinase (PKII) less than 10% of the total cAMP-stimulated kinase activity. Treatment with 8-Cl-cAMP (5 microM, 72 h) decreased PKI to a level below 30% of that in untreated control cells and markedly increased PKII composed of three peaks. Photoaffinity labeling/SDS-polyacrylamide gel electrophoresis of column fractions identified the molecular species of regulatory (R) subunits present in protein kinases. Control cells contained high levels of the 48-kDa protein (RI) that composed PKI and low levels of the 50-kDa RII associated with PKII. 8-Cl-cAMP treatment brought about a decrease in the 48-kDa RI along with an increased formation of the truncated 34-kDa RI associated with PKI and an increase in the 50-54-kDa species of RII associated with PKII. A similar protein kinase profile as that shown by 8-Cl-cAMP treatment was observed in cells infected with the human RII beta retroviral vector: the 48-kDa RI of PKI decreased and the 52- and 54-kDa RII associated with PKII increased as compared with uninfected control cells. However, unlike 8-Cl-cAMP treatment, RII beta retroviral vector infection brought about no increase in the 34-kDa-truncated RI but exhibited an increase in the free 48-kDa RI subunit. As the 48-kDa RI and the 50-kDa RII were present in control cells, the enhanced expression of the 52- and 54-kDa RII proteins was due to overexpression of the RII beta gene. We identified the 48-kDa RI as RI alpha, the 50-kDa RII as RII alpha, the 52-kDa RII as RII beta, and the 54-kDa RII as the phosphorylated form of either the RII alpha or RII beta subunit. In vivo labeling experiments using [3H]8-Cl-cAMP demonstrated that 8-Cl-cAMP enters cells and binds to both PKI and PKII.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

8-氯-cAMP是一种位点选择性的cAMP类似物,可诱导多种人类癌细胞系的细胞类型生长抑制。8-氯-cAMP的这种抑制作用与其差异调节I型和II型cAMP依赖性蛋白激酶的能力有关。在本研究中,我们证明了8-氯-cAMP在HL-60人早幼粒细胞白血病细胞中调节这些激酶同工酶的独特作用机制。高效液相色谱(HPLC)分离了HL-60细胞中存在的各种蛋白激酶同工型。在对照细胞中,I型蛋白激酶(PKI)占总cAMP刺激激酶活性的90%以上,II型蛋白激酶(PKII)占不到10%。用8-氯-cAMP(5 microM,72小时)处理后,PKI降至未处理对照细胞水平的30%以下,并显著增加了由三个峰组成的PKII。柱馏分的光亲和标记/SDS-聚丙烯酰胺凝胶电泳确定了蛋白激酶中存在的调节(R)亚基的分子种类。对照细胞含有高水平的构成PKI的48-kDa蛋白(RI)和低水平的与PKII相关的50-kDa RII。8-氯-cAMP处理导致48-kDa RI减少,同时与PKI相关的截短的34-kDa RI形成增加,与PKII相关的50-54-kDa RII种类增加。在用人类RIIβ逆转录病毒载体感染的细胞中观察到与8-氯-cAMP处理相似的蛋白激酶谱:与未感染对照细胞相比,PKI的48-kDa RI减少,与PKII相关的52-和54-kDa RII增加。然而,与8-氯-cAMP处理不同,RIIβ逆转录病毒载体感染没有导致34-kDa截短的RI增加,但表现出游离48-kDa RI亚基增加。由于对照细胞中存在48-kDa RI和50-kDa RII,52-和54-kDa RII蛋白的表达增强是由于RIIβ基因的过表达。我们将48-kDa RI鉴定为RIα,50-kDa RII鉴定为RIIα,52-kDa RII鉴定为RIIβ,54-kDa RII鉴定为RIIα或RIIβ亚基的磷酸化形式。使用[3H]8-氯-cAMP的体内标记实验表明,8-氯-cAMP进入细胞并与PKI和PKII结合。(摘要截断于400字)

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