McPhee I, Pooley L, Lobban M, Bolger G, Houslay M D
Division of Biochemistry and Molecular Biology, University of Glasgow, Scotland, U.K.
Biochem J. 1995 Sep 15;310 ( Pt 3)(Pt 3):965-74. doi: 10.1042/bj3100965.
COS-7 cells were transfected with a plasmid encoding a putative splice variant of PDE4A cyclic AMP-specific phosphodiesterase, RPDE-6 (RNPDE4A5). This led to the expression of a novel, cyclic AMP-specific, rolipram-inhibited phosphodiesterase activity. In such transfected cells a novel approximately 109 kDa species was recognized by anti-peptide sera raised against a dodecapeptide whose sequence is found at the extreme C-terminus of both RPDE-6 and another PDE4A splice variant. RD1 (RNPDE4A1A). RPDE-6 activity and immunoreactivity was found distributed between both pellet (approximately 25%) and cytosol (approximately 75%) fractions of transfected COS-7 cells. Soluble and pellet RPDE-6 activities exhibited similar low Km values for cyclic AMP (approximately 2.4 microM) and were both inhibited by low concentrations of rolipram, with IC50 values for the soluble activity being lower (approximately 0.16 microM) than for the pellet activity (approximately 1.2 microM). Pellet RPDE-6 was resistant to release by either high NaCl concentrations or the detergent Triton X-100. Probing brain homogenates with the anti-(C-terminal peptide) sera identified two immunoreactive species, namely an approximately 79 kDa species reflecting RD1 and an approximately 109 kDa species that co-migrated with the immunoreactive species seen in COS cells transfected to express RPDE-6. The approximately 109 kDa species was found distributed between both the low-speed (P1) and high-speed (P2) pellet fractions as well as the cytosol fractions derived from both brain and RPDE-6-transfected COS cells. In contrast, RD1 was found exclusively in the P2 fraction. Phosphodiesterase (PDE) activity immuno-precipitated by these antisera from brain cytosol had the characteristics of COS cell-expressed RPDE-6 with KmcyclicAMP approximately 3.7 microM and IC50rolipram approximately 0.12 microM. The distribution of PDE activity immunoprecipitated from the cytosol of various brain regions paralleled that seen for the distribution of the approximately 109 kDa immunoreactive species. It is suggested that the 109 kDa species identified in brain cytosol and pellet fractions is the native form of RPDE-6. The PDE4A splice variants, RD1 and RPDE-6, were shown to have distinct patterns of expression among various brain regions. PDE4A and PDE4B activities appear to provide the major source of PDE4 activity in brain membranes, whereas the cytosolic PDE4 activity is suggested to reflect predominantly the activity of the PDE4D family. Alternative splicing of the PDE4A gene confers distinct N-terminal domains on RPDE-6 and RD1, which attenuates the Vmax. of these enzymes and defines their distinct subcellular distribution pattern.
COS-7细胞用编码磷酸二酯酶4A(PDE4A)环磷酸腺苷特异性磷酸二酯酶的一种假定剪接变体RPDE-6(RNPDE4A5)的质粒进行转染。这导致了一种新型的、环磷酸腺苷特异性的、罗匹尼罗抑制的磷酸二酯酶活性的表达。在这种转染细胞中,一种新型的约109 kDa的蛋白条带被针对一种十二肽产生的抗肽血清所识别,该十二肽的序列位于RPDE-6和另一种PDE4A剪接变体RD1(RNPDE4A1A)的极端C末端。发现RPDE-6的活性和免疫反应性分布在转染的COS-7细胞的沉淀(约25%)和胞质溶胶(约75%)部分之间。可溶性和沉淀的RPDE-6活性对环磷酸腺苷表现出相似低的Km值(约2.4 microM),并且都被低浓度的罗匹尼罗抑制,可溶性活性药物半数抑制浓度(IC50)值(约0.16 microM)低于沉淀活性(约1.2 microM)。沉淀的RPDE-6对高浓度氯化钠或去污剂曲拉通X-100的释放具有抗性。用抗(C末端肽)血清检测脑匀浆,鉴定出两种免疫反应性条带,即反映RD1的约79 kDa条带和与转染表达RPDE-6的COS细胞中所见免疫反应性条带共迁移的约109 kDa条带。发现约109 kDa条带分布在低速(P1)和高速(P2)沉淀部分以及来自脑和转染RPDE-6的COS细胞的胞质溶胶部分。相比之下,RD1仅存在于P2部分。这些抗血清从脑胞质溶胶中免疫沉淀的磷酸二酯酶(PDE)活性具有COS细胞表达的RPDE-6的特征,环磷酸腺苷的Km约为3.7 microM,罗匹尼罗的IC50约为0.12 microM。从各个脑区的胞质溶胶中免疫沉淀的PDE活性分布与约109 kDa免疫反应性条带的分布相似。提示在脑胞质溶胶和沉淀部分中鉴定出的109 kDa条带是RPDE-6的天然形式。PDE4A剪接变体RD1和RPDE-6在各个脑区显示出不同的表达模式。PDE4A和PDE4B活性似乎是脑膜中PDE4活性的主要来源,而胞质溶胶中的PDE4活性主要反映PDE4D家族的活性。PDE4A基因的可变剪接赋予RPDE-6和RD1不同的N末端结构域,这降低了这些酶的最大反应速度(Vmax)并定义了它们不同的亚细胞分布模式。