Biochemical and Evolutionary Significance of Phospholipid Methylation

Abstract

All nucleated mammalian cells synthesize phosphatidylcholine from choline via the CDP-choline pathway. Hepatocytes have a second pathway for the synthesis of phosphatidylcholine, a stepwise methylation of phosphatidylethanolamine, catalyzed by phosphatidylethanolamineN-methyltransferase and encoded by the Pemptgene. We report that when Pempt-deficient mice were fed a choline-deficient diet for 3 days, severe liver pathology occurred apparently due to a lack of phosphatidylcholine biosynthesis. The hepatic concentration of phosphatidylcholine decreased by 50% compared with wild type mice on the diet. The levels of plasma triacylglycerols and cholesterol were decreased by greater than 90% in thePempt-deficient mice. We suggest that the Pemptgene has been maintained during evolution to provide phosphatidylcholine when dietary choline is insufficient, as might occur during starvation or pregnancy. All nucleated mammalian cells synthesize phosphatidylcholine from choline via the CDP-choline pathway. Hepatocytes have a second pathway for the synthesis of phosphatidylcholine, a stepwise methylation of phosphatidylethanolamine, catalyzed by phosphatidylethanolamineN-methyltransferase and encoded by the Pemptgene. We report that when Pempt-deficient mice were fed a choline-deficient diet for 3 days, severe liver pathology occurred apparently due to a lack of phosphatidylcholine biosynthesis. The hepatic concentration of phosphatidylcholine decreased by 50% compared with wild type mice on the diet. The levels of plasma triacylglycerols and cholesterol were decreased by greater than 90% in thePempt-deficient mice. We suggest that the Pemptgene has been maintained during evolution to provide phosphatidylcholine when dietary choline is insufficient, as might occur during starvation or pregnancy. Masochistic Enzymology: Dennis Vance's Work on PhosphatidylcholineJournal of Biological ChemistryVol. 292Issue 11PreviewPurification of Phosphatidylethanolamine N-Methyltransferase from Rat Liver Full-Text PDF Open Access phosphatidylethanolamine N-methyltransferase choline-deficient choline-supplemented high density lipoprotein phosphatidylcholine phosphatidylethanolamine very low density lipoprotein. Hepatocytes in liver have abundant activity for the phosphatidylethanolamine N-methyltransferase (PEMT)1 pathway, whereas other cells and tissues express minimal activities for this enzyme (1Bremer J. Greenberg D.M. Biochim. Biophys. Acta. 1960; 37: 173-175Crossref PubMed Scopus (103) Google Scholar, 2Bremer J. Figard P.H. Greenberg D.M. Biochim. Biophys. Acta. 1960; 43: 477-488Crossref Scopus (166) Google Scholar, 3Vance D.E. Ridgway N.D. Prog. Lipid Res. 1988; 27: 61-79Crossref PubMed Scopus (199) Google Scholar, 4Vance D.E. Walkey C.J. Cui Z. Biochim. Biophys. Acta. 1997; 1348: 142-150Crossref PubMed Scopus (171) Google Scholar). Since the liver possesses the CDP-choline pathway for PC biosynthesis (5Kennedy E.P. Vance D.E. Phosphatidylcholine Metabolism. CRC Press, Boca Raton, FL1989: 1-8Google Scholar), why PEMT has been retained during evolution is not obvious. One clue to the importance of PEMT function arises from studies on choline deficiency. When fed a choline-deficient (CD) diet, rats survive with minimal adverse effects, but develop fatty livers (6Zeisel S.H. J. Nutr. Biochem. 1990; 1: 332-349Crossref PubMed Scopus (88) Google Scholar). Therefore, PEMT might function to maintain PC synthesis and generate choline when dietary supply is insufficient. However, the quantitative significance of the PEMT pathway for production of choline as a catabolic product of PC is unclear, and an alternative pathway for synthesis of choline in mammals has been described in which phosphoethanolamine is methylated to yield phosphocholine (7Andriamampandry C. Freysz L. Kanfer J.N. Dreyfus H. Massarelli R. Biochem. J. 1989; 264: 555-562Crossref PubMed Scopus (28) Google Scholar, 8Andriamampandry C. Freysz L. Kanfer J.N. Dreyfus H. Massarelli R. J. Neurochem. 1991; 56: 1845-1850Crossref PubMed Scopus (11) Google Scholar, 9Andriamampandry C. Massarelli R. Kanfer J.N. Biochem. J. 1992; 288: 267-272Crossref PubMed Scopus (8) Google Scholar). To gain insight into the physiological significance of PE methylation, we created mice that completely lacked PEMT activity by targeted disruption of the Pempt gene (10Walkey C.J. Donohue L.R. Bronson R. Agellon L.B. Vance D.E. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 12880-12885Crossref PubMed Scopus (139) Google Scholar). These studies demonstrated that both hepatic isoforms of PEMT, PEMT1 localized to the endoplasmic reticulum and PEMT2 recovered on the mitochondria associated membrane, were encoded by the same gene and absent fromPempt −/− mice. Under standard laboratory conditions, PEMT-deficient mice are indistinguishable from their normal and heterozygous littermates with respect to development, behavior, and fecundity. Microscopic examination of liver slices from 8-week-old mice revealed no obvious histological abnormalities. No significant differences in the composition of plasma lipoproteins or bile, both of which contain large amounts of PC, were observed. Hepatic phospholipid composition, including the level of PC, was minimally affected by the absence of PEMT. Thus, apparently, the PC generated via the CDP-choline pathway can replace PEMT-derived PC, revealing no obvious physiological role for PE methylation under normal conditions. An important test of the function of the PEMT pathway would be to restrict dietary choline and thereby decrease PC production via the CDP-choline pathway. Would the other pathways that have been reported to make phosphocholine (7Andriamampandry C. Freysz L. Kanfer J.N. Dreyfus H. Massarelli R. Biochem. J. 1989; 264: 555-562Crossref PubMed Scopus (28) Google Scholar, 8Andriamampandry C. Freysz L. Kanfer J.N. Dreyfus H. Massarelli R. J. Neurochem. 1991; 56: 1845-1850Crossref PubMed Scopus (11) Google Scholar, 9Andriamampandry C. Massarelli R. Kanfer J.N. Biochem. J. 1992; 288: 267-272Crossref PubMed Scopus (8) Google Scholar) compensate for the lack of the PEMT pathway? We now report that severe liver pathology rapidly occurs in PEMT-deficient mice after withdrawal of dietary choline for only 3 days. The genotypes of the mice were determined by DNA blotting as described (10Walkey C.J. Donohue L.R. Bronson R. Agellon L.B. Vance D.E. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 12880-12885Crossref PubMed Scopus (139) Google Scholar). Mice of all three genotypes (Pempt +/+,Pempt +/−, and Pempt −/−) had a mixed 129/J and C57Bl/6 genetic background. The colony was maintained on a reversed 12-h light/dark cycle. At 8 weeks of age, mice of both sexes were switched to either a CD semisynthetic diet (ICN, catalog number 901387) or a choline-supplemented (CS) diet (CD diet + 0.4% choline chloride) and fed ad libitum for 60 h, then fasted for 12 h before sacrifice. Liver pieces were fixed in 10% formalin, and sections were stained with hemotoxylin and eosin according to standard methods. Alternatively, liver pieces were fixed by flash-freezing in liquid nitrogen. Frozen sections were stained with Oil Red O. Blood was extracted from the mice by cardiac puncture and plasma separated by centrifugation. All instruments were pretreated with EDTA to prevent coagulation. Plasma from mice fed either diet was pooled according to genotype and assayed for aspartate aminotransferase and alanine aminotransferase activities, using the GP and GO transaminase kit (Sigma-Aldrich). Bile acids in individual plasma samples were assayed using diagnostic kit 450-A (Sigma-Aldrich) adapted for microtiter plate analysis. Livers were homogenized with a motorized glass-Teflon homogenizer in 5 volumes of homogenizing buffer (11Houweling M. Cui Z. Tessitore L. Vance D.E. Biochim. Biophys. Acta. 1997; 1346: 1-9Crossref PubMed Scopus (56) Google Scholar). Protein was determined using the BCA assay (Pierce) using bovine serum albumin as a standard. Lipids were extracted from the homogenates in chloroform-methanol (12Bligh E.G. Dyer W.J. Can. J. Biochem. Physiol. 1959; 37: 911-917Crossref PubMed Scopus (43088) Google Scholar) and separated by thin-layer chromatography. The bands corresponding to PC and triacylglycerol were scraped and assayed (13Bartlett G.R. J. Biol. Chem. 1959; 234: 466-468Abstract Full Text PDF PubMed Google Scholar, 14Snyder F. Stephens N. Biochim. Biophys. Acta. 1959; 34: 244-245Crossref PubMed Scopus (361) Google Scholar), using inorganic phosphate and triolein as standards. The concentration of triacylglycerol in plasma was measured using a diagnostic kit (Sigma-Aldrich) adapted for microtiter analysis. Plasma samples from mice were pooled according to genotype and lipoproteins were separated by high-performance liquid chromatography on a Amersham Pharmacia Biotech Superose 6 column attached to a Beckman System Gold apparatus as described (15Kieft K.A. Bocan T.M.A. Krause B.R. J. Lipid Res. 1991; 32: 859-866Abstract Full Text PDF PubMed Google Scholar). The relative amounts of total glycerol (primarily derived from triacylglycerol) and total cholesterol were determined with an in-line enzymatic assay by mixing column effluent with assay reagents (Sigma-Aldrich diagnostic reagent 337-B for glycerol or reagent 352 for cholesterol) and incubation in a postcolumn reactor. Peaks were identified by comparison with lipoprotein standards. To examine the importance of PE methylation for production of PC and choline (as a catabolic product of PC) in the absence of dietary choline, we fed mice of all three genotypes (Pempt +/+, Pempt +/−, and Pempt −/−) a CD or a CS diet. InPempt −/− mice fed the CD diet, the net biosynthesis of PC could occur only from residual dietary choline already present in the animal or from endogenously synthesized choline (7Andriamampandry C. Freysz L. Kanfer J.N. Dreyfus H. Massarelli R. Biochem. J. 1989; 264: 555-562Crossref PubMed Scopus (28) Google Scholar, 8Andriamampandry C. Freysz L. Kanfer J.N. Dreyfus H. Massarelli R. J. Neurochem. 1991; 56: 1845-1850Crossref PubMed Scopus (11) Google Scholar, 9Andriamampandry C. Massarelli R. Kanfer J.N. Biochem. J. 1992; 288: 267-272Crossref PubMed Scopus (8) Google Scholar). After 3 days, 8-week-old mice of all three genotypes fed the CS diet, and mice fed a CD diet and expressing PEMT activity (Pempt +/+ and Pempt +/−), exhibited a 5–10% weight gain. In contrast,Pempt −/− mice fed a CD diet lost between 5 and 10% of their total body weight and appeared indolent and uncoordinated. At necropsy the livers from thePempt −/− mice were grossly enlarged (∼50% by weight), with a distinct pale color. The gall bladders were also engorged (Fig. 1 A). Other tissues were not visibly altered. The rapid development of the CD-mediated pathology in the Pempt −/− mice was such that the experiments had to be terminated after 3 days to avoid pain or death. Pempt +/+ and Pempt +/− mice fed a CD diet displayed slight peripheral discoloration of the liver (Fig. 1 A), whereas none of the murine genotypes fed a CS diet displayed any abnormal hepatic morphology. Liver sections from mice with and without PEMT, fed CS and CD diets, were examined histopathologically. Livers from thePempt −/− mice fed a CD diet displayed severe vacuolization (Fig. 1 D). Much less vacuolization was observed in Pempt +/+ and Pempt +/− animals fed the CD diet (Fig. 1,B and C). No vacuolization was observed in the livers of any mice fed a CS diet including thePempt −/− mice (Fig. 1 E). Staining of frozen liver sections with lipophilic Oil Red O confirmed the presence of lipids in vacuoles of hepatocytes in all mice fed a CD diet (data not shown). Alanine aminotransferase and aspartate aminotransferase normally reside in hepatocytes but leak into the bloodstream upon liver injury. Therefore, the activities of these enzymes in the plasma is a useful indicator of hepatic damage (16Marshall W.J. Clinical Chemistry. Mosby, London1995: 231Google Scholar). The level of alanine aminotransferase activity in pooled plasma was increased 12.5-fold in Pempt −/− mice on a CD diet compared with normal mice on the same diet (Table I).Pempt −/− mice fed a CS diet had an undetectable plasma alanine aminotransferase activity. A similar pattern was observed for aspartate aminotransferase (Table I). The level of bile acids in the plasma, another indicator of liver damage, was elevated 5.6-fold in Pempt −/− mice fed the CD diet compared with Pempt +/+ mice fed a CD diet (Table I). Moreover, the plasma of Pempt −/− mice fed the CD diet was bright yellow, indicating jaundice. The challenge of PEMT-deficient mice with the CD diet resulted in severe liver damage and clearly demonstrated the importance of PC biosynthesis for proper maintenance of liver function. The presence of low levels of aminotransferases and bile acids in plasma from Pempt +/+ and Pempt +/− mice on the CD diet is consistent with the observed death of cells in livers from rats fed a CD diet (17Shin O.H. J. Cell. Biochem. 1997; 64: 196-208Crossref PubMed Scopus (46) Google Scholar, 18Albright C.D. Liu R. Bethea T.C. Da Costa K.-A. Salganik R.I. Zeisel S.H. FASEB J. 1996; 10: 510-516Crossref PubMed Scopus (94) Google Scholar).Table ICholine deficiency in Pempt−/− mice elevates aminotransferases and bile acids in plasmaCholine-supplemented dietCholine-deficient diet+/++/−−/−+/++/−−/−ALT (IU/l)NDNDND33ND417AST (IU/l)<1<1<12533150Bile acids (μm)<1<1<124 ± 939 ± 13138 ± 43Murine plasma was pooled according to genotype (+/+, +/−, and −/−) and diet, and alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities were assayed. Plasma bile acids were also measured. ND = not detectable. Open table in a new tab Murine plasma was pooled according to genotype (+/+, +/−, and −/−) and diet, and alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities were assayed. Plasma bile acids were also measured. ND = not detectable. Analysis of the hepatic lipids by thin-layer chromatography revealed that the only lipid accumulating in livers of Pempt −/− mice was triacylglycerol. The level of triacylglycerol in the livers from Pempt −/−mice fed a CD diet was increased 3.9-fold (p < 0.05) compared with Pempt −/− mice fed a CS diet (Fig. 2 A). Significant amounts of triacylglycerol did not accumulate in the livers of Pempt +/+ mice fed a CD diet compared with a CS diet even though the gross liver morphology and histology indicated what appeared to be fat deposits (Fig. 1, A and B). This result contrasted with previous studies in which hepatic triacylglycerol accumulated by 6.5-fold in rats fed the CD diet compared with the CS diet (19Yao Z. Vance D.E. Biochem. Cell Biol. 1990; 68: 552-558Crossref PubMed Scopus (99) Google Scholar). 2C. J. Walkey, L. Yu, L. B. Agellon, and D. E. Vance, unpublished results. The rise in bile acid concentration in the plasma of Pempt −/− mice fed the CD diet suggests an increase in hepatic bile acid levels. Previously, the formation of large vacuoles devoid of lipids in response to elevation of intracellular bile acid levels was documented in hepatoma cells (20Torchia E.C. Agellon L.B. Eur. J. Cell Biol. 1997; 74: 190-196PubMed Google Scholar). Hence, the unusual liver morphology of thePempt −/− mice fed a CD diet is not solely a consequence of fat accumulation. Moreover, the gross liver morphology of the Pempt −/− mice is distinct from that observed for livers from mice that overexpress a truncated sterol response element binding protein-1a, which was attributed to massive accumulation of lipid (21Shimano H. Horton J.D. Hammer R.E. Shimomura I. Brown M.S. Goldstein J.L. J. Clin. Invest. 1996; 98: 1575-1584Crossref PubMed Scopus (699) Google Scholar). The livers of these latter animals also did not exhibit signs of cell death, which occurred in the livers fromPempt −/− mice on the CD diet. The consequences of impaired PC biosynthesis, through the simultaneous elimination of both dietary choline and PE methylation, on the amounts of hepatic phospholipids were determined. After 3 days, total hepatic phospholipids decreased by 41.6% (p < 0.05) from 125.4 to 73.2 nmol/mg of protein for Pempt −/−mice fed the CS compared with the CD diet. The amount of hepatic PC was even more dramatically decreased (56.4%) in Pempt −/− mice (from 63.3 on the CS diet to 27.6 nmol/mg of protein on the CD diet) (Fig. 2 B). PC is an important component of lipoproteins, forming a monolayer around the neutral lipid core of the particles, enhancing their solubility in plasma. The fatty liver observed in rats fed a CD diet could be, at least partially, ascribed to a defect in secretion of triacylglycerol-rich very low density lipoproteins (VLDL) from the liver, resulting in hepatic triacylglycerol accumulation (22Haines D.S.M. Can. J. Biochem. 1966; 44: 45-57Crossref PubMed Scopus (21) Google Scholar, 23Yao Z. Vance D.E. J. Biol. Chem. 1988; 263: 2998-3004Abstract Full Text PDF PubMed Google Scholar). Plasma VLDL from Pempt +/− mice contained less triacylglycerol than did VLDL from wild type mice (Fig. 3 A), a result that matches the total plasma triacylglycerol values. The amount of plasma triacylglycerol in Pempt −/− mice on the CS diet was 43.6 ± 12.3 mg/dl, and the values forPempt +/+ and Pempt +/−mice on a CS diet, and of Pempt +/+ mice on a CD diet, were similar. The values for plasma triacylglcyerol forPempt +/− mice (30.2 ± 8.0 mg/dl) and Pempt −/− mice (28.6 ± 7.3 mg/dl) on the CD diet were significantly different (p < 0.05) from the Pempt +/+ mice on a CD diet.Pempt −/− mice contained very little triacylglycerol in the VLDL fraction. Instead, triacylglycerol was detected in a more dense fraction of lipoproteins having the same density as low density lipoproteins. Whether or not the reduction in circulating triacylglycerol-rich lipoproteins is due to decreased VLDL secretion from the liver or increased clearance of lipoproteins is not known. As in Pempt +/+ mice, the majority of plasma cholesterol in Pempt +/− mice fed the CD diet is found in high density lipoprotein (HDL) (Fig. 3 B).Pempt −/− mice had greatly reduced levels of HDL cholesterol, which might be due to defective formation of nascent HDL as a result of decreased availability and/or efflux of PC from tissues. In addition, formation of HDL in the plasma might be impaired as a result of decreased levels of VLDL and chylomicrons, which act as lipid donors for HDL (24Glickman R.M. Sabesin S.M. Arias I.M. The Liver: Biology and Pathobiology. Raven Press, Ltd., New York1994: 391-414Google Scholar). The rapid onset of damage to the liver, but not to other tissues, can be ascribed to the high demand for choline and PC for normal hepatic function. Hepatic choline can be phosphorylated and enter the CDP-choline biosynthetic pathway or, in liver, can be oxidized to betaine, which is an important source of methyl groups for other metabolic pathways (25Zeisel S.H. Blusztajn J.K. Annu. Rev. Nutr. 1994; 14: 269-296Crossref PubMed Scopus (614) Google Scholar). The liver also secretes lipoproteins and bile, which require large amounts of PC as the major phospholipid. For example, the amount of biliary PC that is secreted from the liver is ∼23 mg/day for a 20 g mouse (26Kuipers F. Elferink R.P.J.O. Verkade H.J. Groen A.K. Bitman R. Subcellular Biochemistry. 28. Plenum Press, New York1997: 295-318Google Scholar). The weight of liver in a 20-g mouse is ∼2 g, and the total amount of PC in this liver would be ∼20 the mouse liver secretes into bile the of hepatic of PC during a of that PC is by the as and is to the liver and other tissues (26Kuipers F. Elferink R.P.J.O. Verkade H.J. Groen A.K. Bitman R. Subcellular Biochemistry. 28. Plenum Press, New York1997: 295-318Google Scholar). Hence, the of PC for bile secretion might be a major for the 50% in PC levels in liver after only 3 days. In addition, secretion of PC with lipoproteins and of choline to also on the PC in The to PEMT in liver from an important role for this enzyme during starvation and during and other animals fat and as but not The concentration of plasma choline in decreased from ± to (p < after a L. Zeisel S.H. J. Clin. Nutr. 1997; PubMed Scopus Google Scholar). When animals of starvation choline the function of thePempt gene is to important for of PC for metabolic The experiments that the elimination of PE methylation greatly the consequences of choline deficiency. These also that no alternative pathway, other than phospholipid methylation or the CDP-choline pathway, is of quantitative significance for PC or choline in mice. Thus, the decreased PC biosynthesis in Pempt −/− mice fed the CD diet in the of hepatic PC which rapidly to liver We that a function of PE methylation is to both hepatic synthesis of PC and production of the choline derived from PC during Zeisel S.H. Z. Costa K.A. J. Nutr. Google Scholar) reported that and a severe on the levels of in the For example, during the of hepatic betaine, and choline decreased by 50% or more in CD compared with CS The decrease in these was even more in though PEMT deficiency not decrease of these mice under laboratory conditions, the of PEMT would be a significant for of and choline were We that PEMT PC and choline when dietary choline is insufficient. The PEMT-deficient mice are also a for liver the is the onset of to be We and N. for We are to Vance and Zeisel for and