Circulating oxidized LDL, increased in patients with acute myocardial infarction, is accompanied by heavily modified HDL.

Oxidized LDL (oxLDL) is a known risk factor for atherogenesis. This study aimed to reveal structural features of oxLDL present in human circulation related to atherosclerosis. When LDL was fractionated on an anion-exchange column, in vivo-oxLDL, detected by the anti-oxidized PC (oxPC) mAb, was recovered in flow-through and electronegative LDL [LDL(-)] fractions. The amount of the electronegative in vivo-oxLDL, namely oxLDL in the LDL(-) fraction, present in patients with acute MI was 3-fold higher than that observed in healthy subjects. Surprisingly, the LDL(-) fraction contained apoA1 in addition to apoB, and HDL-sized particles were observed with transmission electron microscopy. In LDL(-) fractions, acrolein adducts were identified at all lysine residues in apoA1, with only a small number of acrolein-modified residues identified in apoB. The amount of oxPC adducts of apoB was higher in the LDL(-) than in the L1 fraction, as determined using Western blotting. The electronegative in vivo-oxLDL was immunologically purified from the LDL(-) fraction with an anti-oxPC mAb. The majority of PC species were not oxidized, whereas oxPC and lysoPC did not accumulate. Here, we propose that there are two types of in vivo-oxLDL in human circulating plasma and the electronegative in vivo-oxLDL accompanies oxidized HDL.

PLA 2 ) (35,36). Oxidation of HDL decreases the capability to inhibit LDL oxidation, and its anti-atherogenic properties change drastically to pro-atherogenic properties. Huang et al. (37) have revealed that oxidized apoA1containing modifications generated by MPO-dependent reactions accumulate in human atherosclerotic plaques. Therefore, it should be noted that oxidized HDL (ox-HDL) could be an important atherosclerotic risk factor, as well as oxLDL.
The purpose of this study is to clarify the structural features of in vivo-oxLDL. We focused on in vivo-oxLDL of patients with AMI, comparing it with that of healthy subjects. The criterion of in vivo-oxLDL in this study is modified with oxPC based on its antigenicity against anti-oxPC mAb. Our data demonstrated that there are two types of in vivo-oxLDL in human plasma, which were separated on anion-exchange chromatography. In vivo oxLDL in the LDL() fraction was more abundant in patients with AMI than in healthy subjects. In addition, the LDL() fraction contained heavily modified apoA1 and oxPC-modified apoB. The LDL() fraction was shown to be a mixture of LDL-and HDL-sized particles by electron microscopy. These features are distinct from Cu-oxLDL prepared in vitro.

Isolation of human lipoproteins from patients with AMI and healthy subjects
This study was conducted in accordance with the principles of the Declaration of Helsinki and was approved by the Ethical Committee of Showa University (No. 214), with informed consent obtained from all healthy subjects and patients before the study. Plasma samples were separated from the blood of seven healthy volunteers (age 22-56 years), after a 12 h overnight fast, by centrifugation at 700 g for 15 min, after which EDTA was added to the plasma (final concentration 0.25 mM) and immediately used. Twenty-five patients with AMI (age 25-85 years; 23 patients presented ST-segment elevation MI and two patients had non-ST-segment elevation MI) received cardiac catheter treatment at 818 Journal of Lipid Research Volume 61, 2020 Showa University Hospital, and then, aliquots of blood samples suctioned from the site of infarction were used in this study. Sera obtained from the blood samples were collected after centrifugation and stored at 80°C until analysis.
Total LDL and HDL were prepared as described previously (12). Briefly, LDL (1.019 < d < 1.063 g/ml) and HDL (1.063 < d <1.210 g/ml) fractions were separated from the healthy plasma using ultracentrifugation (Himac CS150GX, HITACHI), with the addition of KBr to adjust the density, and then dialyzed three times against PBS containing 0.25 mM EDTA to remove the KBr. LDL and HDL fractions of AMI patients were isolated from pooled sera, where each batch of the patients' sera was prepared from three to six individuals. The protein concentrations of LDL and HDL were determined by the BCA method using BSA as standard. All lipoprotein samples were maintained under Ar gas at 4°C until analysis to avoid spontaneous oxidation. To minimize possible damage during storage, analyses of lipids or proteins of all lipoprotein samples were performed within 1 week after isolation.

In vitro modification of LDL
In vitro Cu-oxLDL was prepared by oxidation of LDL from healthy subjects (0.2 mg protein per milliliter), with 5 M copper sulfate for 3 h at 37°C, according to the method previously described (11) with few modifications.

Separation of LDL subfractions on anion-exchange chromatography
LDL collected from plasma or serum was fractionated into subfractions using anion-exchange chromatography as reported previously (29). Tandem Q-Sepharose Fast Flow 7/25 mm columns (GE Healthcare, Chicago, IL) were connected to a peristaltic pump. The counter-ion was introduced by washing the columns with 10 ml of elution buffer B [10 mmol/l Tris-HCl, 1 mol/l NaCl, 1 mmol/l EDTA (pH7.4)], and then equilibrated with 20 ml of buffer A [10 mmol/l Tris-HCl, 1 mmol/l EDTA (pH 7.4)]. The LDL was replaced in buffer A using a PD-10 desalting column (Bio-Rad, Hercules, CA), and then 3-4 mg protein of LDL was injected into Q-Fast Flow columns at a flow rate of 1 ml/min. The ratio of buffer B to buffer A was increased in a stepwise manner, and eluates collected as 1 ml aliquots were kept on ice. The flowthrough fraction was named L1, and the eluted fraction (using 0.5 mol/l NaCl) was termed LDL(), referring to electronegative LDL. The elution buffers were degassed before the column elution; samples and recovered fractions were maintained under Ar gas. The absorbance of each fraction was measured at 280 nm using NanoDrop 2000c (Thermo Fisher Scientific, Waltham, MA).

Determination of oxLDL and apoB levels by sandwich ELISA
The oxLDL and apoB contents in the fractions eluted from Q-Fast Flow columns were determined using a sandwich ELISA method previously described (11). Briefly, microtiter wells (Costor ® 3369, Corning) were precoated with 1.0 g/100 l of DLH3 or 0.5 g/100 l of anti-apoB-100 mAb for more than 2 h at room temperature. The plates were blocked with 1% BSA-TBS, and then 100 l of diluted or undiluted column elution fractions were added overnight at 4°C. After extensive washing, the oxLDL or LDL captured in the wells was detected with antihuman apoB-100 pAb (sheep IgG) and alkaline phosphataseconjugated anti-sheep IgG pAb (donkey IgG). In each microtiter plate, either diluted Cu-oxLDL (0.1-3 ng/well) or diluted LDL (0.5-10 ng/well) were run simultaneously to determine the standard curves.

Gel electrophoresis and immunoblotting analysis
The samples for electrophoresis were concentrated to the required amount using ultrafiltration membranes (Amicon ® Ultra 10K device; Merck, Darmstadt, Germany) when necessary. Native PAGE was performed on 3-20% Tris-glycine gels loaded with 2 g of protein per lane and run at 20 mA for 1.5 h under nondenaturing conditions with Tris-glycine buffer. For the agarose gel electromobility assay, 0.6% agarose gels were loaded with 12 g of protein per lane and run at 50 V for 2 h on ice using barbital buffer at pH 8.6. The agarose gels were stained with Coomassie Brilliant Blue stain. Proteins were separated either on native PAGE gels or on agarose gels, and then they were transferred to PVDF membranes and probed with antibodies against oxPC, apoB, or apoA1. The blots were detected by enhanced chemiluminescence (ECL Prime; GE Healthcare) or ImmunoStar LD (Fujifilm Wako).

Electron microscopy
Lipoprotein particles present in the L1 and LDL() fractions were observed microscopically using a Hitachi H7600 transmission electron microscope (HITACHI, Tokyo, Japan). After anion exchange chromatography, lipoprotein samples were diluted to <0.01 g/l. Samples were absorbed on carbon-coated grids and processed for negative staining with 2% uranyl acetate solution, pH 7.0.
The particle size of lipoproteins was measured using ImageJ software. The ranges of LDL and HDL were defined as 16.0-31.3 nm and 7.6-16.0 nm based on the literature regarding the classification of lipoprotein subclasses (39).

Affinity extraction of in vivo-oxLDL by an anti-oxPC mAb
The microtiter wells (Costor ® 3369) were precoated with 1.0 g/100 l of DLH3 or monoclonal IgM  isotype control at room temperature for 2 h. The plate was blocked with Pierce™ blocking buffer (#37572; Thermo Fisher) for 1 h, and then incubated with the L1 or LDL() fractions and Cu-oxLDL solution overnight at 4°C. After washing with cold-PBS three times, the lipids in the lipoproteins bound to the antibodies were extracted with 100% ethanol containing internal standard lipids (1,2-didecanoyl-sn-glycero-3-phosphocholine and 1-pentadecanoyl-2-hydroxy-sn-glycero-3-phosphocholine). Similarly, proteins bound to the antibody-coated microtiter wells were extracted with 50 mM Tris-HCl, pH 8.0, containing 0.1% SDS.

Detection of oxidatively modified amino acid residues by LC-MS/MS
Analysis of the oxidative modification of apolipoproteins using LC-MS/MS was carried out according to the method previously reported (23). After agarose gel electrophoresis, blotted proteins on the PVDF membrane were stained with Ponceau-S solution, and the protein bands were dissected. In vivo-oxLDL separated from the L1 and LDL() fractions using anti-oxPC mAb was spotted on PVDF membranes (5 × 5 mm). All PVDF membrane pieces were washed with chloroform/methanol (1/1, v/v) to deplete lipids. Then, the lipid-depleted proteins were reduced with 10 mM dithiothreitol/80 mM ammonium hydrogen carbonate/20% acetonitrile for 1 h at 60°C and alkylated with 55 mM iodoacetamide/80 mM ammonium hydrogen carbonate/20% acetonitrile for 45 min at room temperature in the dark. After washing with Milli-Q water followed by 2% acetonitrile/Milli-Q water, the proteins were digested with 1 g trypsin/70% acetonitrile/30 mM ammonium hydrogen carbonate overnight at 37°C. The tryptic digests were extracted twice with 1% formic acid/70% acetonitrile and dried in a SpeedVac evaporator. The extracted peptides were dissolved in 0.1% formic acid and analyzed using a DiNa Nano-LC system (KYA Tech Co., Tokyo, Japan) coupled online with Triple TOF 5600 (Sciex, Framingham, MA), as described previously (40). The oxidized peptides were identified using Pro-teinPilot™ version 4.5 software (Sciex). The search engine and sequence database used were Paragon™ Algorithm 4.5.0.0, 1654, and UniProt, respectively. The number of entries in the database was 15,908. The protease used was trypsin that cleaves the C-terminal end of lysine and arginine residues. At most, five missed cleavages were permitted. Mass tolerance for precursor ion and that for fragment ion were both 0.05. Threshold score/expected value was set at 1.30/95% (Unused Prot Score). All fixed and variable modifications attached are listed in supplemental Table S1. The original proteome datasets were deposited to JPOST project number JPST000758 (https://globe.jpostdb.org/entry/JPST000758).

Analysis of PC molecular species by LC-MS/MS
Lipids were quantified using a LC-MS/MS system (QTRAP5500, Sciex; coupled to a Shimadzu Prominence HPLC system). Normal-phase HPLC, for the analysis of PCs, was performed on an Inertsil SIL-100A column with the elution solvent acetonitrile/ methanol/3% formic acid (18:11:1, v/v/v) as described previously (24). The samples were dried under N 2 gas, dissolved in 100 l of mobile phase solvent, and 10 l of the sample were injected. The PCs were detected by multiple reaction monitoring in which 42 elected ions that released fragment ions of m/z = 184.1 were detected simultaneously (supplemental Table S2). The relative amount of PC species in in vivo-oxLDL was calculated semi-quantitatively, and the amounts of PCs that bound to monoclonal IgM  isotype control as nonspecific reaction were subtracted.

Statistical analysis
Statistical analysis was performed using JMP Pro13 software.
Statistical differences between groups were tested by the nonparametric Mann-Whitney U test. For comparisons across multiple groups, the data were analyzed using the parametric Tukey-Kramer test and nonparametric Dunn's test. Data compared with control was analyzed using the parametric Dunnett's test. A value of P < 0.05 was considered statistically significant.

Elution profiles of oxLDL on an anion-exchange column
LDL fractions from AMI patients and healthy subjects were fractionated on the anion-exchange column (Fig. 1). The absorbance of eluates from the column at 280 nm showed four peaks corresponding to the stepwise separation. The first peak at fraction numbers 3-5 is referred to as the L1 fraction, which is the flow-through fraction, and the fourth peak at fraction numbers 25-27 is referred to as the LDL(), which was eluted from the column using 0.5 M NaCl. The absorbance for the LDL() fraction in AMI patients was 2-to 3-fold higher than that in healthy subjects. ApoB was detected in all four peaks and oxLDL was detected mostly in the L1 and LDL() fractions when the elution profiles of apoB and oxLDL were examined by sandwich ELISA (Fig. 1A, B). The concentration of oxLDL in the LDL() fraction was approximately 3-fold higher in AMI patients than in healthy subjects. The oxLDL/apoB ratios of the LDL() fraction in AMI patients and healthy controls were 3-and 6-fold higher than those observed in the L1 fraction, respectively. The use of plasma or serum made a minimal difference because the elution profiles of LDL separated from the plasma and serum from healthy subjects were well-matched with each other (Fig. 1A, C).

ApoB protein in the LDL() fraction shows increased oxPC modifications
Oxidative modifications of apoB protein in the L1 and LDL() fractions were detected by native PAGE followed by immunoblotting. Modification of apoB with oxPC was more abundant in the LDL() fractions than in the L1 fractions in both healthy and AMI samples (Fig. 2).

Electromobility of apoB protein in the LDL() fraction of AMI patients
Electrophoretic mobility in agarose gels of the L1 and LDL() fractions and Cu-oxLDL were compared to evaluate the extent of apoB protein denaturation ( Fig. 3A-C). Previous experiments showed that electromobility of LDL markedly shifted toward the anode in agarose gel electrophoresis by copper-induced oxidation (24). Interestingly, the LDL() fraction contained two bands. ApoB appeared to be the lower band in the Western blot ( Fig. 3A, C). In AMI patients, there was a statistically significant difference in the electromobilities between the LDL() and L1 fractions ( Fig. 3B). ApoB in the LDL() fractions tended to shift farther than in the L1 fractions. ApoB in the LDL() fractions had lower electromobility than did Cu-oxLDL, not only in healthy subjects but also in AMI patients. However, Cu-oxLDL eluted at the same fractions as LDL() from the anion-exchange column (Fig. 1D). The electronegative property of LDL() in this fraction may not be solely attributed to apoB modification.

Presence of HDL in the LDL() fraction
To identify the proteins in upper bands detected only in LDL() fractions (Fig. 3A), both upper and lower bands were analyzed by LC-MS/MS with ProteinPilot software. The numbers of identified protein species, except for trypsin, are shown in Table 1. Within these identified proteins, only apoA1, apoE, and apoB peptides had greater confidence than trypsin peptides (Table 1). ApoE is known to associate with LDL and large HDL particles. Accordingly, the presence of apoA1 and apoE suggested that HDL particles were recovered in the LDL() fractions of both healthy subjects and AMI patients, although the LDL fraction was separated from HDL by ultracentrifugation before the anion-exchange column. In addition, the HDL fraction, separated by ultracentrifugation, eluted mostly at fraction number 15 when subjected to the anion-exchange column (Fig. 1D). The presence of apoA1 in the upper band of the LDL() fractions was verified by Western blotting (Fig. 3D).
To examine the morphological properties of lipoprotein particles detected in the LDL() fractions, direct observation of lipoproteins in the L1 and LDL() fractions using transmission electron microscopy (TEM) was performed (Fig. 4). In the L1 fractions, most of the particles were LDL, circular with a diameter over 20 nm, and similar results were observed in both AMI patients and healthy subjects. On the contrary, many smaller particles, as well as LDL particles, were observed in the LDL() fraction. The diameter of the particles observed in the L1 and LDL() fractions from healthy and AMI samples together with the HDL fraction from healthy subjects were measured (Fig. 4C). Compared with LDL particles in the LDL() fractions, the particle size of LDL in the L1 fractions was significantly larger. The LDL() from healthy subjects contained intermediate-sized particles (15-19 nm), and the mean diameter of HDL particles was significantly different from that of from AMI patients. Although a few HDL particles were in close contact with LDL particles (Fig. 4A, black arrows), most of particles were separately present.

ApoA1 in the LDL() fraction is oxidatively modified
The apoA1 in the LDL() fractions shifted higher in the agarose gel than that in native HDL (Fig. 3D), suggesting the presence of oxidatively modified apoA1 in the LDL() fraction, which may contribute to the electronegative properties of this fraction.
Oxidatively modified amino acid residues of apoA1 were analyzed using ProteinPilot software following the identification of the proteins, and those of apoA1in the LDL() fraction and the control HDL fraction were compared. In the apoA1 present in the LDL() fraction, a wide variety of oxidized amino acid residues of apoA1 were identified, with the total number of sites of oxidized amino acid residues significantly higher when compared with native HDL ( Table 2). The %Cov of each analysis of apoA1, which is the percentage of matching amino acids from identified peptide signals within the total number of amino acids in the sequence, was >80%. ApoA1 contains 21 lysine residues among 243 amino acids, and acrolein or MDA adducts were detected at nearly all the lysine residues in apoA1 in the LDL() fractions of healthy subjects as well as AMI patients (Table 2). According to the review by Shao (41), the levels of modified apoA1 peptides, including chloro-tyrosine and nitro-tyrosine, are elevated in circulating HDL from CAD patients. These halogenated amino acids were found in a few peptides in apoA1 in the LDL() fraction (Table 2). Figure 5 shows the MS/MS spectra identifying peptides modified with nitrotyrosine, chlorotyrosine, and the hydroxynonenal-adduct of lysine residues. Although quantitative evaluation could not be applied to this analysis, it is likely that adducts of reactive lipid aldehydes to lysine residues increased in apoA1 in the LDL() fractions when compared with native HDL (supplemental Tables S3-S7).

PC profile of in vivo-oxLDL
In vivo-oxLDL bound to anti-oxPC mAb was collected from the L1 or LDL() fractions, and the profiles of PC  molecular species were determined by LC-MS/MS. Similarly, in vitro-oxLDL exhibiting antigenicity to anti-oxPC mAb was extracted from Cu-oxLDL and PC molecular species were analyzed. Figure 6 shows the relative amount of each PC species in oxLDL in L1 and LDL() from AMI patients and healthy subjects and in in vitro-oxLDL. The PC species are classified into five categories. Among the nonoxidized PC in in vivo-oxLDL, PC34:2 (m/z = 758.6) was the highest, followed by PC34:1 (m/z = 760.6) and PC36:2 (m/z = 786.6) (Fig. 6A, C). The long-chain oxPC species derived from PC34:2 and PC36:4 were marginally increased in oxLDL in the LDL() of AMI patients (Fig. 6D). Among cleaved oxPC species, oxPC650 [representative species is 1-palmitoyl-2-(9-oxo-nonanoly) PC; m/z = 650.6] was the most detected in the in vivo-oxLDL of healthy subjects but not AMI patients (Fig. 6E). The major lysoPC species, 16:0-LPC and 18:0-LPC, were detected in the in vivo-oxLDL obtained from AMI patients as well as in vitro oxLDL; however, their contents in the in vivo-oxLDL from healthy subjects were low (Fig. 6B). LysoPC demonstrated a good contrast with oxPC650, which was high in the oxLDL from healthy subject but low in AMI patients. Overall, the PC species was most detected in oxLDL in the LDL() of AMI patients, implying that the amount of oxLDL bound to the anti-oxPC mAb was the highest in the LDL() of AMI patients. However, most of the PC species in in vivo-ox-LDL were nonoxidized PCs, and lysoPC and cleaved oxPC did not accumulate. On the contrary, lysoPC accounted for a considerably higher percentage in in vitro-oxLDL separated from Cu-oxLDL, where the profile of PC species was in good agreement with our previous results (24).

Identification of oxidatively modified apoB amino acid residues in in vivo-oxLDL
The in vivo-oxLDL separated from the LDL() and L1 fractions was recovered by SDS solution, and apoB peptides were analyzed by LC-MS/MS. Table 3 shows the list of oxidized amino acid residues in in vivo-oxLDL. The sequence coverage of apoB using this procedure was only 30-40% for oxLDL in the L1 of AMI patients and Cu-oxLDL, and more than 50% for others. Acrolein and MDA-modified lysine residues were identified from samples captured by anti-oxPC mAb, and many of the modified lysine residues were found in certain domains in apoB (approximately residues 1-1,000, 2,100-2,570, and 4,050-4,500). ApoB in the in vivo-oxLDL particles contained modified amino acid residues comparable to some extent to those observed in oxPC-positive Cu-oxLDL (supplemental Tables S8-S17).

DISCUSSION
A large volume of evidence to show the involvement of oxLDL in the initiation and progression of atherosclerosis has accumulated over the past quarter century. However, a few critical questions remain unanswered, including establishing the actual form of in vivo-oxLDL. In this study, we succeeded in separating in vivo-oxLDL from the blood of healthy subjects and patients with AMI and investigated its characteristics. The in vivo-oxLDL recognized by the anti-oxPC mAb was divided into two types, oxLDL in L1 and oxLDL in LDL(). To the best of our knowledge, this is the first study to directly indicate that in vivo-oxLDL consisted of at least two unique fractions, distinct from in vitro Cu-oxLDL. In addition, our data indicated the presence of heavily modified HDL in the LDL() fraction.
Several research groups have investigated in vivo-modified LDLs, like electronegative LDL and lipoprotein (a) [Lp(a)], that fit well with the oxLDL hypothesis. Avogaro, Bon, and Cazzolato (42) first demonstrated that LDL() can be separated using anion-exchange chromatography, and the reported LDL() particles may be heterogeneously aggregated in a way independent of S-S bonds. LDL() has been characterized by increased electronegativity, phospholipolysis, and the presence of many apolipoproteins, in addition to apoB (43)(44)(45). Additionally, it has an ability to stimulate endothelial cells through the LOX-1 receptor (46,47). In our study, it was demonstrated that LDL() contained one type of oxPC-positive in vivo-oxLDL. One of the major findings of this study was that oxHDL accompanied in vivo-oxLDL in the LDL() fraction. This was supported by the following reasons: First, while the LDL fraction (d = 1.019-1.063) was separated from other lipoproteins by ultracentrifugation, oxHDL was recovered in the LDL() fraction. Second, the control HDL fraction was mostly eluted at 0.22 mol/l NaCl, whereas the LDL() fraction was eluted at 0.5 mol/l NaCl. Remarkably, the apoA1 in the LDL() fraction was heavily modified. Gao and Podrez (48) have reported that apoA1 is also susceptible to oxidative modifications based on a precise analysis of modified apoA1 peptides. Therefore, it Proteins contained in the L1 and LDL() fractions of healthy subjects and AMI patients were separated using 0.6% agarose gel electromobility (Fig. 3A) and transferred to PVDF membrane. The protein bands on the PVDF membrane detected with Ponceau-S staining were dissected and digested with trypsin. Peptides extracted from the PVDF membrane were dissolved in 0.1% formic acid and analyzed using LC-MS/MS. N indicates the rank of the specified protein within the list of all the detected proteins in each band. %Cov indicates the percentage of matching amino acids from identified peptide signals within the total number of amino acids in the sequence. The data are representative results of each of the multiple replicates (n = 3).
is likely that the electronegative property of oxLDL in LDL() was due to, at least in part, its association with ox-HDL. LDL-and HDL-sized particles were mostly separated under TEM, and they were separately electrophoresed on agarose gel. The association between them was possibly electrostatic interaction, but not covalent binding.
HDL is considered to be anti-atherosclerotic and antioxidative. However, recent advances in HDL investigations have revealed more complex and pivotal roles of HDL in atherogenesis (34). The presence of chlorinated and nitrated oxHDL, which are MPO-dependent modifications, in human atherosclerotic lesions as well as plasma has been reported (37,49,50). An ELISA system using the recombinant LOX-1 receptor showed the presence of oxidatively modified HDL in human plasma (51).
Reportedly, a significant association exists between plasma oxHDL and inflammatory states in patients with psoriasis (52). Notably, HDL turns to atherogenic once it is oxidatively modified. Our current observations included a characteristic of oxHDL in vivo; oxHDL could interact with oxLDL and work together as electronegative lipoproteins.
Our current data showed that, in patients with AMI, the oxLDL concentration in the LDL() fraction was about 3-fold higher than in healthy subjects, as determined by sandwich ELISA (Fig. 1). The blood samples of AMI patients were collected from the infarct regions during catheter treatments. It is possible that oxLDL in LDL(), at least in part, is derived from the ruptured plaque at the acute phase, corresponding with the current hypothesis regarding the origin of circulating oxLDL based on the transient increase of plasma

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Journal of Lipid Research Volume 61, 2020 oxLDL levels in patients with AMI (19,22). Hazen and colleagues have reported the presence of oxHDL in the plasma and in atherosclerotic plaques, while modified apoA1 in atherosclerotic lesions was lipid-poor and aggregated (37,50). These distinct features of modified apoA1 in the plaque failed to correspond with oxHDL in the LDL() fraction. The oxHDL that associates with oxLDL in the LDL() fraction might be generated in circulation presumably through the interaction of HDL with oxLDL.
The electronegative in vivo-oxLDL, namely oxLDL in LDL(), contains oxLDL and heavily modified oxHDL. Interestingly, the apoB in this fraction is immune-positive to anti-oxPC mAb but has fewer oxidatively modified amino acid residues than apoA1. In our previous study, the apoB fragments modified with oxPC became resistant to lysosomal hydrolysis, staying longer in macrophage-derived foam cells (53). Thus, increased oxPC-apoB adducts in the LDL() fraction could be derived from accumulated oxLDL in foam cells. Another type of oxLDL existed in the L1 fractions of healthy subjects as well as AMI patients. The oxLDL in the L1 fraction demonstrated a marginal increase in electromobility and minimal apoB modification with oxPC but contained comparable amounts of extractable oxPC. These characteristics correspond to MM-LDL (25,26,54). While heavily oxidized LDL is quickly cleared from the circulation by the liver (55), MM-LDL binds to the LDL receptor but not to scavenger receptors, remaining in circulation longer than the heavily oxidized LDL. In addition to the acute diffusion of oxidized lipoproteins from the ruptured plaque and quick clearance by the liver, oxidized lipoproteins might spontaneously transfer between arterial tissue and circulation (22).
When LDL is treated with copper sulfate, both lipids and proteins are extensively modified. The accumulation of oxidative modifications of apoB amino acids, oxidized lipids,   Tables S3-S7 for detailed results. and lysoPC, as well as a significant increase in the negative charge in Cu-oxLDL particles, were observed (23,24). Interestingly, apoB in LDL() is covalently modified with oxPC, whereas the site of modified amino acid residues in apoB is minimal, and the electronegative property of the LDL is moderate. In addition, the amounts of oxPC and lysoPC in in vivo-oxLDL were substantially lower compared with in vitro-oxLDL. The preparation of Cu-oxLDL in a small test tube in which only LDL is present in a limited volume of buffer could be the reason for the differences. During the oxidation process in vitro, any intermediate products, including reactive aldehydes and oxPC, remain in a closed system and easily react with proteins; whereas, under in vivo conditions, oxidative intermediates formed in the LDL particles diffuse into the circulation or transfer to other lipoproteins. Because HDL has protective effects toward LDL oxidation (56), HDL is likely to interact with LDL particles to protect them from further oxidative modification by transferring oxPCs from LDL to HDL and by scavenging radicals with apoA1 molecules. This antioxidative action of HDL against oxLDL may lead to oxHDL generation (57).
We observed that apoA1 in LDL() was heavily modified with acrolein. This was consistent with a previous report showing preferable modification of apoA1 with acrolein in plasma HDL (48). Acrolein is a lipid peroxidation product; however, it is also produced through the enzymatic action of MPO (58). Because inflammatory responses occur in atheromatous plaques, MPO derived from macrophages and neutrophils could participate in the process of acrolein modification of lipoproteins.
Because the LDL() fraction could contain heterogeneous forms of lipoproteins, we separated oxPC-bound ox-LDL particles in the LDL() and L1 fractions to analyze their molecular features. Notably, modifications of apoB amino acid residues were limited in both fractions. The profiles of extracted PC molecular species demonstrated little difference among oxLDL in L1 or LDL() from AMI patients or healthy controls, except for POVPC (m/z = 650) and lysoPC (Fig. 6). The lysoPC in in vivo-oxLDL could be produced by hydrolysis of cleaved oxPC by Lp-PLA 2 . A meta-analysis on Lp-PLA 2 levels revealed that the enzyme activity and mass were associated with long-term risks of CHD events (59). In this study, Lp-PLA 2 activity in the LDL fraction was higher in AMI patients than in healthy subjects (AMI patients: 16.8 U/l vs. healthy subjects: 11.6 U/l), and the cleaved oxPC could be hydrolyzed enzymatically. Compared with Cu-oxLDL, the contents of oxPCs and lysoPC were much smaller, suggesting that the oxidative change in the in vivo-oxLDL was limited. Furthermore, it has been proposed that the smaller HDL subfraction, HDL3, mediates reduction of PCOOH to PCOH of LDL utilizing methionine residues of apoA1, so that oxidation of LDL lipids may be prevented by HDL3 (35). In addition, it is possible that oxPC or lysoPC generated in oxLDL can transfer between two lipoproteins, e.g., oxLDL and HDL particles, and this functional interaction can yield oxHDL (34,57). Currently, we are attempting to elucidate the transfer action of oxPC and lysoPC between lipoproteins using stable isotope-labeled probes.
Lp(a) is more electronegative than LDL and is a known risk factor for atherosclerosis (60)(61)(62). The density of Lp(a) ranges between 1.050 and 1.082 g/ml, distributed in both LDL and HDL fractions by density gradient ultracentrifugation. One previous report has proposed a model in which LDL() (referred to as L5) contains several apolipoproteins, including apoA1 and apo(a) in addition to apoB in its particle (63). Our LC-MS/MS analysis of the LDL() lower bands, identified apoE and apoA1 in addition to apoB; however, apo(a) was identified as one of the minor proteins, which is consistent with previous reports (29,30). In our LDL() samples, any lipoproteins with particle size 32.5-40 nm corresponding to Lp(a) were not found by TEM. Additionally, it is known that the serum concentration of Lp(a) has great variety among different ethnic groups; the Lp(a) concentration in the Asian population is lower than other ethnic groups (62). Although we cannot rule out the presence of Lp(a) in the LDL() fraction, we consider its contribution would be limited.
In addition to apoA1, HDL contains some other apolipoproteins like apoA2. Recently, it was reported that HDL particles containing apoA2 have different properties from those without apoA2 (64). Although apoA2 was detected in the LDL() fraction as a minor constituent in our experiments, it is possible that a subclass of HDL may have a selective contribution to the HDL-LDL complex.
Several studies have shown that small dense LDL (sdLDL) is an atherogenic subfraction of LDL (65,66). It is hypothesized that sdLDL is susceptible to oxidative modification; however, direct proof remains unavailable. From the TEM images of the LDL() fraction, we observed that it consists of mainly HDL and normal-sized LDL; however, LDL() from healthy subjects may in part contain smaller-sized LDL that corresponds to sdLDL. More work is needed to clarify the relationship between sdLDL and in vivo-oxLDL.
Our current study succeeded in separating in vivo-oxLDL from human plasma. We observed that there are two forms of in vivo-oxLDL, one of them, oxLDL in L1, contains oxPC but is not electronegative and the other, oxLDL in LDL(), is modified covalently with oxPC and is electronegative, presumably due to association with heavily oxidized HDL. The latter oxLDL increased in the acute phase of AMI patients. Both of these oxLDLs demonstrated different features from Cu-oxLDL. There might be many different forms of in vivo-oxLDL; however, our observations clearly provide new insights into the structural features of in vivo-oxLDL and help in understanding the mechanisms of atherogenesis.

Data availability
The original proteome datasets together with the list of identified peptides were deposited to JPOST (https:// repository.jpostdb.org/entry/JPST000758). All other data is contained in the article.
The authors gratefully acknowledge the work of past and present members of the Division of Biological Chemistry who contributed to this study. Without their contribution, this work would not have been possible. The authors would like to thank Editage (www.editage.com) for English language editing. Oxidatively modified apoB peptides in oxLDL bound to anti-oxPC mAb were identified by LC-MS/MS. L1, LDL() from healthy subjects and AMI patients, and Cu-oxLDL were added to microtiter wells precoated with anti-oxPC mAb, and the antigens bound to the mAb were subjected to LC-MS/MS analysis. Proteins bound to IgM  isotype control were recovered simultaneously with the nonspecific reaction. oxLDL possessing antigenicity against the anti-oxPC mAb in in vitro Cu-oxLDL was also extracted under the same conditions. The proteins spotted onto PVDF membranes were digested by trypsin followed by reductive alkylation, and extracted peptides were analyzed by LC-MS/MS. ApoB peptides with modifications were identified using ProteinPilot software. The table shows oxidatively modified apoB-100 amino acid residues that were identified in two different experiments. The amino acid residues with an asterisk (*) were also detected in the control wells that were precoated with monoclonal IgM  isotype control. The name of the original amino acid residue was written in one-letter code; (K), lysine; (P), proline; (R), arginine; (W), tryptophan. See supplemental Tables S8-S17 for detailed results.