Manganiello V C, Taira M, Degerman E, Belfrage P
Pulmonary/Critical Care Medicine Branch, NHLBI, NIH, MD 20892, USA.
Cell Signal. 1995 Jul;7(5):445-55. doi: 10.1016/0898-6568(95)00017-j.
Seven different but related cyclic nucleotide phosphodiesterase (PDE) gene families have been identified. Type III cGMP-inhibited (cGI) PDEs, the PDE3 gene family, are found in many tissues. cGI PDEs exhibit a high affinity for both cAMP and cGMP, and are selectively and relatively specifically inhibited by certain agents which augment myocardial contractility, promote smooth muscle relaxation and inhibit platelet aggregation. Adipocyte, platelet, and hepatocyte cGI PDE activities are regulated by cAMP-dependent phosphorylation. Insulin-induced phosphorylation/activation of adipocyte and hepatocyte cGI PDEs is thought to be important in acute regulation of triglyceride and glycogen metabolism by insulin. Two distinct cGI PDE subfamilies, products of distinct but related genes, have been identified. They exhibit the domain structure common to PDEs with a carboxyterminal region, conserved catalytic domain and divergent regulatory domain. In their catalytic domains cGI PDEs contain a 44 amino acid insertion not found in other PDE families. The expression of cGIP1 and cGIP2 mRNAs differs in different rat tissues, suggesting distinct functions for the two cGI PDE subfamilies, i.e., cGIP1 in adipose tissue, liver, testis and cGIP2 in myocardium, platelets and smooth muscle.
现已鉴定出七个不同但相关的环核苷酸磷酸二酯酶(PDE)基因家族。III型cGMP抑制性(cGI)PDE,即PDE3基因家族,存在于许多组织中。cGI PDE对cAMP和cGMP均表现出高亲和力,并被某些增强心肌收缩力、促进平滑肌松弛和抑制血小板聚集的药物选择性且相对特异性地抑制。脂肪细胞、血小板和肝细胞的cGI PDE活性受cAMP依赖性磷酸化调节。胰岛素诱导的脂肪细胞和肝细胞cGI PDE磷酸化/激活被认为在胰岛素对甘油三酯和糖原代谢的急性调节中起重要作用。已鉴定出两个不同的cGI PDE亚家族,它们是不同但相关基因的产物。它们具有PDE共有的结构域结构,包括羧基末端区域、保守的催化结构域和不同的调节结构域。在其催化结构域中,cGI PDE含有一个在其他PDE家族中未发现的44个氨基酸的插入序列。cGIP1和cGIP2 mRNA在不同大鼠组织中的表达不同,表明这两个cGI PDE亚家族具有不同的功能,即cGIP1在脂肪组织、肝脏、睾丸中表达,cGIP2在心肌、血小板和平滑肌中表达。