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J. Biol. Chem., Vol. 282, Issue 46, 33237-33241, November 16, 2007
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From the Canadian Institutes of Health Research Group on the Molecular and Cell Biology of Lipids and the Department of Biochemistry, University of Alberta, Edmonton, Alberta T6G 2S2, Canada
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INTRODUCTION |
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Biochemical Characterization of PEMT |
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 TOPINTRODUCTION Biochemical Characterization of... PEMT and Its Evolutionary...PEMT, Steatosis, and...PEMT and Lipoprotein HomeostasisPEMT and HomocysteinePEMT and Gene ExpressionConclusionREFERENCES |
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PEMT and Its Evolutionary Significance |
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die early during embryogenesis (12). Another gene (Pcyt1b) encodes the isoform CT
(13). Deletion of the part of this gene that encodes CT2 is not embryonically lethal but does result in gonadal dysfunction (14). CT accounts for 
85% of the CT activity in the liver (15). Because the liver has ample PC biosynthetic capacity via the CDP-choline pathway, why did PEMT survive in evolution? In the 1990s, the obvious and unambiguous approach to answer this question was to construct mice that lacked PEMT. The PEMT gene is localized to chromosome 11 and spans 25 kb with seven exons and six introns (16). A targeting vector was constructed and introduced into mice, yielding homozygous PEMT gene-disrupted mice (17). All PEMT activity was eliminated in the Pemt–/– mice, yet the levels of hepatic PC and PE were minimally affected. Pemt–/– mice displayed no abnormal phenotype, normal hepatocyte morphology, normal plasma lipid levels, and no differences in bile composition. Thus, it seemed that PEMT was dispensable. This result was not unanticipated because the CDP-choline pathway remained in the livers of Pemt–/– mice. To attenuate PC biosynthesis via the CDP-choline pathway, we fed the mice a choline-deficient (CD) diet. After 3 days, the CD-Pemt–/– mice exhibited end-stage liver failure (18). The concentration of PC in the liver decreased by 50% compared with that in CD-Pemt+/+ mice, and the concentrations of plasma triacyglycerols (TG) and cholesterol were decreased by >90%. These data suggest that PEMT has survived in evolution to provide PC and/or choline (derived from PC via catabolism) at times when choline is insufficient in the diet (19).
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PEMT, Steatosis, and Steatohepatitis |
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The dramatic decrease in hepatic PC in CD-Pemt–/– mice (19) caused us to consider how this might occur. The liver secretes lipoproteins and bile that utilize large amounts of PC. The biliary PC that is secreted from the liver is 23 mg/day for a 20-g mouse (22). The total amount of PC in the liver would be 20 mg. Thus, each day the mouse liver secretes into the bile the equivalent of its entire pool of PC. When PC replenishment is compromised, as in the CD-Pemt–/– mice, the rapid decrease in hepatic PC is not unexpected. PC biosynthesis is also required for normal very low density lipoprotein (VLDL) secretion (23). In an attempt to estimate the relative importance of PEMT-derived PC to VLDL secretion, we traced the fate of [3H-methyl]methionine after injection into the tail vein of a mouse. After 5 h, 5–7% of the radioactivity was recovered in plasma PC compared with 2–6.5% recovered in bile PC (24). Thus, utilization of PEMT-derived PC for lipoprotein secretion is highly significant.
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One difference that became apparent was that the levels of hepatic PE did not decrease in the Pemt–/– mice fed the CD diet, whereas the levels of PE did decrease in the livers of Pemt–/–/Mdr2–/– mice (27). Thus, the ratio of PC to PE decreased from 1.8 to 0.8 in the livers of Pemt–/– mice compared with 1.4 in the livers of Pemt–/–/Mdr2–/–. There was a striking correlation (r = 0.95) between the decreased PC/PE ratio and the plasma content of alanine aminotransferase (a hepatic enzyme that indicates membrane permeability or hepatotoxicity when recovered in plasma). The decreased PC/PE ratio was also found in purified preparations of plasma membranes from the livers of Pemt–/–/Mdr2–/– mice (27). The levels of sphingomyelin and cholesterol did not change in the livers of Pemt–/– and Pemt–/–/Mdr2–/– mice.
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As an additional test that a decreased PC/PE ratio in hepatocytes increases membrane permeability, we used RNA interference against CTP:phosphoethanolamine cytidylyltransferase to inhibit the biosynthesis of PE in hepatocytes derived from CD-Pemt–/– mice (27). Under these conditions, the PE levels decreased and the PC/PE ratio increased in hepatocytes from CD-Pemt–/– mice concomitant with attenuated release of alanine aminotransferase into the medium (27). Similarly, when the RNA interference vector was injected into the tail veins of CD-Pemt–/– mice, steatohepatitis was attenuated; the PC/PE ratio increased; and there was a 75% reduction in plasma alanine aminotransferase.
The results provide strong support for the hypothesis that CD-Pemt–/– mice develop steatohepatitis because of increased permeability of the cell membrane that occurs due to a decreased ratio of PC to PE. Studies on the development of nonalcoholic steatohepatitis in humans have shown that patients with this disease have a significant reduction (p = 0.001) in the PC/PE ratio in hepatic biopsies (27).
A correlation between PEMT and hepatic steatosis has also been observed in a strain of mice with impaired biosynthesis of PC via both pathways (30). This strain, RCS8, showed decreased hyperglycemia and hyperinsulinemia when treated with the diabetic drug rosiglitazone. Treatment of RCS8 mice with rosiglitazone further inhibited PEMT as well as enzymes in the choline pathway with enhanced hepatosteatosis. Rosiglitazone effects on PEMT have since been shown to be dependent on peroxisome proliferator-activated receptor-
action (31). The regulation of PEMT appears to be complicated because induction of type I diabetes by streptozotocin increases PEMT expression (32). Treatment of diabetic rats with insulin prevents the increase in PEMT activity. Thus, there might be a direct relationship between PEMT activity and insulin action. To test this hypothesis, we evaluated the susceptibility of Pemt–/– mice to diet-induced obesity. Whereas Pemt+/+ mice showed weight gain, plasma hyperlipidemia, and insulin resistance, Pemt–/– mice were strikingly protected against these changes.5
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PEMT and Lipoprotein Homeostasis |
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With the generation of Pemt–/– mice, the role of PEMT in the secretion of VLDL was examined. Secretion of TG was decreased by 50% in cultured hepatocytes derived from male Pemt–/– compared with Pemt+/+ mice (37). In agreement, there was a 70% inhibition of secretion of apoB100, but not apoB48. Complementary experiments in which a cDNA for PEMT was transfected into McArdle rat hepatoma cells (which lack PEMT) showed a stimulation of TG secretion (37). Studies in mice showed that male, but not female, Pemt–/– mice had lower levels of TG, apoB100, and apoB48 in plasma (38). Measurement of secretion of apoB100 in the livers of male Pemt–/– mice showed a decrease compared with Pemt+/+ mice. The reason for this sexual dimorphism is not evident (24).
Because the PEMT pathway is necessary, at least in male mice, for normal VLDL secretion, we wondered if the CT pathway for PC biosynthesis is also required. We generated mice that specifically lacked CT in liver hepatocytes (15). Compared with wild-type mice, these mice had lower levels of serum TG, PC, and apoB100 and exhibited a decreased secretion of VLDL into plasma independent of gender. Interestingly, there was an almost 2-fold increase in the activity of PEMT that did not compensate for the loss of CT activity (15). Thus, both pathways for PC biosynthesis are independently required for VLDL secretion.
Because the levels of VLDL were decreased in the plasma of PEMT mice, we were curious if Pemt–/– mice might be protected against atherosclerosis. Because mice do not readily develop atherosclerosis, we bred the Pemt–/– mice with atherosclerosis-prone mice that lacked the low density lipoprotein receptor and fed the mice a high fat/high cholesterol diet for 16 weeks. There was a striking 85% decrease in atherosclerosis in the Pemt–/–/low density lipoprotein receptor knock-out mice compared with the Pemt+/+/low density lipoprotein receptor knock-out mice.5
The major lipoprotein in mice is high density lipoprotein (HDL). The levels of cholesterol and PC of HDL were also decreased in both genders of Pemt–/– mice (38). Similarly, the levels of HDL-associated lipids were decreased by 50% in the liver-specific CT knock-out mice (15). One possible mechanism for why PEMT deficiency results in a decrease in HDL lipids is that efflux of lipids to plasma apoA-I was impaired. However, this was not altered in hepatocytes from Pemt–/– mice.6 Rather, there was increased expression of a receptor for HDL, scavenger receptor class B, type I, and this increased the removal of HDL lipids from the medium of hepatocytes.6
HDL appears to have an important role in hepatic PC homeostasis. When Pemt–/– mice are fed a CD diet, male mice show signs of liver damage within 24 h, whereas female mice do not (39). By 2 days of choline deficiency, liver damage is evident in both male and female Pemt–/– mice. A potential explanation for the gender difference is that in the female mice, there is an increase in plasma HDL during the first day of choline deficiency, and some of the HDL-associated PC is delivered to the liver (39). HDL is implicated in "reverse cholesterol transport," in which cholesterol from extrahepatic tissues is delivered to the liver, where it can be converted into bile acids and excreted. From the data available to date, it seems that HDL also delivers PC to the liver and participates in hepatic PC homeostasis.
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PEMT and Homocysteine |
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It is clear that biological methylation and Hcy metabolism are closely related. At present, there are 50–100 known mammalian methyltransferases (21). This number might be an underestimate because a bioinformatics analysis has shown that 0.6–1.6% of open reading frames in microbial, plant, and animal genomes might encode methyltransferases (21). Because PEMT accounts for the formation of 30% PC made in the liver and 3 AdoHcy molecules are synthesized for every PC molecule generated, we hypothesized that PEMT might contribute significantly to plasma Hcy. Remarkably, deletion of PEMT decreased circulating Hcy by 50% (45). Moreover, hepatocytes isolated from Pemt–/– mice secreted less Hcy into the medium than did hepatocytes from littermate controls. Because PEMT deficiency does not change the levels of enzymes involved in metabolizing Hcy and because the levels of hepatic AdoMet and AdoHcy were unaltered, we concluded that PEMT activity directly regulates plasma Hcy levels (45).
McArdle RH-7777 cells have negligible PEMT activity. Reconstitution of PEMT activity in McArdle cells stimulated Hcy secretion into the medium compared with vector-transfected cells (45). Mutagenesis of lysine 197 in the C-terminal ER retrieval motif of PEMT resulted in re-localization of PEMT from the ER to the Golgi. This "mistargeting" of PEMT did not influence Hcy production (46). Thus, Hcy secretion was directly proportional to the levels of PEMT expression independent of cellular localization.
In the liver-specific CT knock-out mice, PEMT activity was increased nearly 2-fold above control levels (15). In agreement with our paradigm, increased PE methylation stimulated Hcy production in CT-deficient hepatocytes (47). Consequently, the liver-specific CT knock-out mice developed mild (20–40%) hyperhomocysteinemia. Unlike in Pemt–/– mice, both hepatic betaine:Hcy methyltransferase and methionine adenosyltransferase were stimulated in the liver-specific CT knock-out mouse, and [14C]PC production from [14C-methyl]betaine was increased 1.7-fold in CT knock-out hepatocytes (47). These data suggest that betaine production from choline oxidation is increased in knock-out hepatocytes in an attempt to secure enough AdoMet for the increased rate of PE methylation.
Using data published by Reo et al. (48), we estimated that the amount of AdoMet utilized to synthesize PEMT-derived PC would be 108–150 µmol/250-g rat/day (47). It has been long thought that the synthesis of creatine from guanidinoacetate consumes the majority of AdoMet in rodents (49) and humans. However, the rate of creatine loss (in the form of urinary creatinine) has been measured at 60 µmol/250-g rat/day (50), which suggests that PEMT, rather than creatine synthesis, is a quantitatively more important source of Hcy in rodents. The contribution of PEMT to Hcy production in humans is debatable (51–54). Mudd et al. (51, 52) suggested that PE methylation consumes 15% (or 2.5 mmol/day) of available AdoMet. However, current estimates indicate that 5 mmol of PC is secreted into bile each day in a typical human (55–57). Approximately one-third of this PC (1.65 mmol) is probably generated by the PEMT reaction (48, 58). Hence, to satisfy PC production, the PEMT reaction might consume 5 mmol of AdoMet/day, which is 2-fold higher than the original estimate for PEMT-dependent AdoMet consumption. Clearly, PEMT is a major player in AdoMet consumption and Hcy production in addition to its role in PC biosynthesis and function.
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PEMT and Gene Expression |
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-estradiol for 24 h. There was an increase in mRNA, protein, and PEMT activity in a dose-dependent manner. An estrogen response element was found. These results provide the first indication as to why premenopausal women are more protected against choline deficiency than are men or postmenopausal women. A polymorphism in the human PEMT gene is associated with nonalcoholic fatty liver disease (60). Controls and patients with liver disease were evaluated for a Val-to-Met substitution at residue 175 of the PEMT human protein. Met/Met at position 175 occurred in 68% of the patients with liver disease and in 41% of control subjects. Dong et al. (61) found a similar association of the V175M polymorphism and liver disease. In apparent contrast, no association was found between the V175M polymorphism and steatosis in the Dallas Heart Study (62). The patients examined in the Dallas Heart Study included multiple races (63), whereas in the study by Song et al. (60), most subjects were Caucasian. When only Caucasian subjects were compared, there was a similar relationship between the V175M polymorphism and liver disease (63). Because not all of the subjects had steatosis, the polymorphism does not necessarily lead to fatty liver. Rather, the polymorphism may predispose people to fatty liver when TG synthesis is enhanced (63).
When the wild-type versus V175M PEMT was expressed in McArdle hepatoma cells, there was 40% less activity (60). It was not possible to measure PEMT activity in the patients. Whether or not the level of PEMT protein determines the rate of the PEMT reaction has not been clearly determined in rodents or humans.
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Conclusion |
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FOOTNOTES |
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2 Present Address: Dept. of Genetics, School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
3 Recipient of postdoctoral fellowships from the Canadian Institutes of Health Research and the Alberta Heritage Foundation for Medical Research.
1 Holder of the Canada Research Chair in Molecular and Cell Biology of Lipids and Scientist of the Alberta Heritage Foundation for Medical Research. To whom correspondence should be addressed. E-mail: dennis.vance{at}ualberta.ca.
4 The abbreviations used are: PE, phosphatidylethanolamine; PC, phosphatidylcholine; PEMT, phosphatidylethanolamine N-methyltransferase; ER, endoplasmic reticulum; AdoMet, S-adenosylmethionine; CT, CTP:phosphocholine cytidylyltransferase; CD, choline-deficient; TG, triacyglycerol(s); VLDL, very low density lipoprotein; HDL, high density lipoprotein; AdoHcy, S-adenosylhomocysteine; Hcy, homocysteine.
5 Y. Zhao and D. E. Vance, unpublished data.
6 J. Robichaud and D. E. Vance, unpublished data.
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