Expression of three isoforms of cGMP-binding cGMP-specific phosphodiesterase (PDES) in human penile cavernosum

被引:125
作者
Lin, CS [1 ]
Lau, A [1 ]
Tu, R [1 ]
Lue, TF [1 ]
机构
[1] Univ Calif San Francisco, Knuppe Mol Urol Lab, Dept Urol, San Francisco, CA 94143 USA
关键词
D O I
10.1006/bbrc.2000.2187
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inhibition of cGMP-specific phosphodiesterase type V (PDEB) has been shown to improve penile erection in patients with erectile dysfunction, We report here the cloning of three PDEB isoforms from human penile tissues. Two of the isoforms were identical to PDE5A1 and PDE5A2, respectively, which had been isolated from nonpenile tissues. The third isoform was novel and hence called PDE5A3, The deduced amino acid sequence of PDE5A3 was the same as the C-terminal 823-residue sequence of PDE5A1 and PDE5A2. While PDE5A1 and A2 isoforms were expressed in all tissues examined, the A3 isoform was confined to tissues with a smooth muscle or cardiac muscle component, When expressed in COS-7 cells, PDE5A1, A2, and A3 isoforms had similar cGMP-catalytic activities with K-m of 6.2, 5.75, and 6.06 mu M, respectively. Their cGMP-catalytic activities were inhibited by zaprinast with IC50 values of 3.2 mu M, 1.3 mu M, and 1.6 mu M, respectively, and by sildenafil with IC50 of 28, 14, and 13 nM, respectively. (C) 2000 Academic Press.
引用
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页码:628 / 635
页数:8
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