Identification of multiple phosphoinositide-specific phospholipases D as new regulatory enzymes for phosphatidylinositol 3,4,5-trisphosphate

被引:20
作者
Ching, TT [1 ]
Wang, DS [1 ]
Hsu, AL [1 ]
Lu, PJ [1 ]
Chen, CS [1 ]
机构
[1] Univ Kentucky, Coll Pharm, Div Pharmaceut Sci, ASTeCC Facil, Lexington, KY 40506 USA
关键词
D O I
10.1074/jbc.274.13.8611
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
In the course of delineating the regulatory mechanism underlying phosphatidylinositol 3,4,5-trisphosphate (PI(3,4,5)P-3) metabolism, we have discovered three distinct phosphoinositide-specific phospholipase D (PI-PLD) isozymes from rat brain, tentatively designated as PI-PLD, PI-PLDb, and PI-PLDc. These enzymes convert [H-3]PI(3,4,5)P-3 to generate a novel inositol phosphate, D-myo [H-3]inositol 3,4,5-trisphosphate ([H-3]Ins(3,4,5)P-3) and phosphatidic acid. These isozymes are predominantly associated with the cytosol, a notable difference from phosphatidylcholine PLDs. They are partially purified by a three-step procedure consisting of DEAE, heparin, and Sephacryl S-200 chromatography. PI-PLDa and PI-PLDb display a high degree of substrate specificity for PI(3,4,5)P-3, with a relative potency of PI(3,4,5)P-3 >> phosphatidylinositol 3-phosphate (PI(3)P) or phosphatidylinositol 4-phosphate (PI(4)P) > phosphatidylinositol 4,5-bisphosphate (PI(4,5)P-3) > phosphatidylinositol 3,4-bisphosphate (PI(3,4)P-3). In contrast, PI-PLDc preferentially utilizes PI(3)P as substrate, followed by, in sequence, PI(3,4,5)P-3, PI(C)P, PI(3,4)P-2, and PI(4,5)P-2. Both PI(3,4)P-2 and PI(4,5)P-2 are poor substrates for all three isozymes, indicating that the regulatory mechanisms underlying these phosphoinositides are different from that of PI(3,4,5)P-3. None of these enzymes reacts with phosphatidylcholine, phosphatidylserine, or phosphatidylethanolamine. All three PI-PLDs are Ca2+-dependent. Among them, PI-PLDb and PI-PLDc show maximum activities within a sub-mu M range (0.3 and 0.9 mu M Ca2+ respectively), whereas PI-PLDa exhibits an optimal [Ca2+] at 20 mu M. In contrast to PC-PLD, Mg2+ has no significant effect on the enzyme activity. All three enzymes require sodium deoxycholate for optimal activities; other detergents examined including Triton X-100 and Nonidet P-40 are, however, inhibitory. In addition, PI(4,5)P-2 stimulates these isozymes in a dose-dependent manner. Enhancement in the enzyme activity is noted only when the molar ratio of PI(4,5)P-2 to PI(3,4,5)P-3 is between 1:1 and 2:1.
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页码:8611 / 8617
页数:7
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