Properties of the delta-, epsilon-, and zeta- Subspecies of Protein Kinase C

蛋白激酶 C δ、ε 和 zeta 亚种的特性

• 批准号: 03670142
• 负责人: KIKKAWA Ushio
• 金额: $ 1.34万
• 依托单位: Kobe University
• 依托单位国家: 日本
• 项目类别: Grant-in-Aid for General Scientific Research (C)
• 财政年份: 1991
• 资助国家: 日本
• 起止时间: 1991 至 1992
• 项目状态: 已结题
• 来源: https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-03670142/
• 关键词: Protein Kinase C; Signal Transduction; Protein Phosphorylation; Diacylglycerol; プロテインキナ-ゼC; ジアシルグリセロ-ル

Protein kinase C plays crucial roles in signal transduction, and is a family of multiple subspecies. This study aimed to investigate the roles of the delta-, epsilon-, and zeta-subspecies, that are initially isolated from brain libraries by the analysis of cDNA clones. The delta-and epsilon-subspecies were purified to homogeneity from rat brain and shown to be dependent on diacylglycerol and phospholipid, but do not require calcium ion for their kinase activities. In addition, these two subspecies showed distinct enzymatic properties, the activity of the epsilon-subspecies is enhanced by fatty acids, whereas the delta-subspecies is inhibited. CHO cell lines overproducing each protein kinase C subspecies were established to study the effects of this enzyme family on cell phenotypes. The growth of the cells overproducing the delta-subspecies was markedly inhibited upon treatment with phorbol 12-myristate 13-acetate that is a potent activator of the protein kinase C family, whereas the cell lines expressing other subspecies were not significantly affected. These results suggest that each subspecies of protein kinase C family has distinct roles in growth regulation. As it was difficult to purify the zeta-subspecies form rat tissues, this subspecies was expressed with the baculovirus system and will be purified from the extract of the infected Sf9 cells. The delta- and epsilon-subspecies were also expressed in the insect cells. We are planning to prepare polyclonal antibodies against these subspecies to investigate the roles of the protein kinase C family by immunological procedures.

蛋白激酶C在信号转导中起着至关重要的作用，是一个多个亚种的家族。本研究的目的是调查的作用，δ-，ε-和ζ-亚种，最初从脑文库中分离的cDNA克隆的分析。δ-和ε-亚种从大鼠脑中纯化至同质，并显示依赖于二酰甘油和磷脂，但不需要钙离子来进行激酶活性。此外，这两个亚种表现出不同的酶特性，ε-亚种的活性被脂肪酸增强，而δ-亚种被抑制。建立了过量生产每个蛋白激酶C亚种的CHO细胞系，以研究该酶家族对细胞表型的影响。过量生产的δ-亚种的细胞的生长显着抑制后，与佛波醇12-肉豆蔻酸酯13-乙酸酯，这是一种有效的激活剂的蛋白激酶C家族的治疗，而表达其他亚种的细胞系没有显着的影响。这些结果表明，蛋白激酶C家族的每个亚种在生长调节中具有不同的作用。由于难以从大鼠组织中纯化ζ-亚种，因此用杆状病毒系统表达该亚种，并将从感染的Sf 9细胞的提取物中纯化。δ-和ε-亚种也在昆虫细胞中表达。我们正计划制备针对这些亚种的多克隆抗体，通过免疫学方法研究蛋白激酶C家族的作用。

项目成果

Ogita, K., Ono, Y., Kikkawa, U., and Nishizuka, Y.: "Expression, separation, and assay of protein kinase C subspecies." Methods Enzymol.200. 228-234 (1991)

Ogita, K.、Ono, Y.、Kikkawa, U. 和 Nishizuka, Y.：“蛋白激酶 C 亚种的表达、分离和测定。”

Watanabe,T.: "Cell division arrest induced by phobol ester in CHO cells overexpressing protein kinase C-δsubspecies" Proc,Natl.Acad.Sci.USA. 89. 10-10163 (1992)

Watanabe，T.：“在过表达蛋白激酶 C-δ 亚种的 CHO 细胞中由佛波酯诱导的细胞分裂”，Proc，Natl Sci，89. 10-10163 (1992)。

OGITA,K.: "Expression,separation,and assay of protein kinase C" Methods Enzymol.200. 228-234 (1991)

OGITA,K.：“蛋白激酶 C 的表达、分离和测定”Methods Enzymol.200。

Koide,H.: "Isolation and characterization of the Σ-subspecies of protein kinase C from rat brain" Proc.Natl.Acad.Sci.USA. 89. 1149-1153 (1992)

Koide，H.：“大鼠脑中蛋白激酶 C 亚种的分离和表征”，美国国家科学院院刊 89。1149-1153。

Iwai,T.: "Catalytic properties of yeast protein kinase C: difference between the yeast and mammalian enzymes" J.Biochem.112. 7-10 (1992)

Iwai,T.：“酵母蛋白激酶 C 的催化特性：酵母和哺乳动物酶之间的差异”J.Biochem.112。