|Home | About | Journals | Submit | Contact Us | Français|
Whereas hepatocytes secrete the major human plasma high density lipoproteins (HDL)-protein, apo A-I, as lipid-free and lipidated species, the biogenic itineraries of apo A-II and apo E are unknown. Human plasma and HepG2 cell-derived apo A-II and apo E occur as monomers, homodimers and heterodimers. Dimerization of apo A-II, which is more lipophilic than apo A-I, is catalyzed by lipid surfaces. Thus, we hypothesized that lipidation of intracellular and secreted apo A-II exceeds that of apo A-I, and once lipidated, apo A-II dimerizes. Fractionation of HepG2 cell lysate and media by size exclusion chromatography showed that intracellular apo A-II and apo E are fully lipidated and occur on nascent HDL and VLDL respectively, while only 45% of intracellular apo A-I is lipidated. Secreted apo A-II and apo E occur on small HDL and on LDL and large HDL respectively. HDL particles containing both apo A-II and apo A-I form only after secretion from both HepG2 and Huh7 hepatoma cells. Apo A-II dimerizes intracellularly while intracellular apo E is monomeric but after secretion associates with HDL and subsequently dimerizes. Thus, HDL apolipoproteins A-I, A-II and E have distinct intracellular and post-secretory pathways of hepatic lipidation and dimerization in the process of HDL formation. These early forms of HDL are expected to follow different apolipoprotein-specific pathways through plasma remodeling and reverse cholesterol transport.
Human plasma high-density lipoproteins-cholesterol is a negative risk factor for cardiovascular disease for which current therapies are inadequate . HDL promote reverse cholesterol transport (RCT) by carrying excess cellular cholesterol through the plasma compartment for disposal by the liver , inhibit LDL oxidation , and are anti-inflammatory . Most plasma HDL are spherical particles with a neutral lipid core surrounded by a surface monolayer of apolipoproteins, cholesterol and phospholipids . Apo A-I and apo A-II are 64% and 20% of HDL-protein mass . Some HDL particles contain only apo A-I (LpAI); most of the remainder contain both apo A-I and apo A-II (LpA-I/A-II) . Formation of LpA-I/LpA-II in plasma occurs via LCAT-mediated fusion of nascent discoidal apo A-II HDL with small spherical LpA-I  or by displacement of apo AI by the more lipophilic apo A-II [8, 9, 10]. Intracellular formation has not been fully delineated. Apo E, a minor HDL protein, preferentially associates with large HDL [11, 12, 13]. The distributions of HDL apolipoproteins, which are exchangeable, are modified by LCAT, CETP, PLTP and hepatic lipase . Indeed, HDL structural remodeling and apo A-I dissociation are essential to RCT [2, 15].
Apo A-I is antiatherogenic, promoting RCT, activating LCAT, and inducing regression of atherosclerotic lesions [16, 17, 18]. Whereas studies of mice over-expressing apo A-II reveal both anti- and pro-atherogenic activities [19, 20], a recent study showed that apo A-II level is inversely associated with risk for atherosclerosis . Human apo A-II is distinguished by Cys6, which forms disulfide-linked dimers [22, 23]. Homodimeric apo A-II is more lipophilic than the monomer, giving it distinct properties ; >96% of human plasma apo A-II is dimeric. Apo A-II dimerization, which is slow in aqueous buffer , is catalyzed ~7500-fold by lipid surfaces . Apo E, which occurs in three isoforms with different cysteine contents, mediates hepatic clearance of apo B-containing lipoproteins  and promotes RCT . Apo E3 (Cys112, Arg158), the most common isoform, is synthesized by HepG2 cells, and in plasma of E3 homozygotes about 55% of the apo E3 is homodimeric or heterodimeric with apo A-II [28, 29].
Hepatocytes synthesize and secrete HDL apolipoproteins [30, 19]; ~20% of apo A-I is lipidated intracellularly with additional lipidation occurring after secretion [31, 32, 33, 34]. The corresponding intracellular lipidation itineraries of apo A-II and apo E have not been reported . Given the mechanistic link between apo A-II lipidation and dimerization, we investigated the synergism between these processes in lipoprotein biogenesis in HepG2 and Huh7 cells and found that apolipoproteins A-I, A-II and apo E are uniquely distributed among intracellular and newly secreted lipoproteins.
Human hepatoma HepG2 cells (American Type Culture Collection, Manassas, VA) and Huh7 cells (kindly provided by Dr. Yumin Xu in Dr. Boris Yoffe’s laboratory, Baylor College of Medicine, Houston, TX) were cultured in MEM (InVitrogen, Carlsbad, CA) with 10% FBS, 1 mM sodium pyruvate and penicillin-streptomycin antibiotics (10 U/mL, 10 μg/mL respectively) (InVitrogen, Carlsbad, CA). Cells were plated and grown to about 80% confluency, washed twice with PBS, incubated with serum-free MEM, and then cells and media were harvested for analysis. Two time points were chosen, one relatively early (2 h) and one relatively late (24 h) after secretion. The early 2 h media is enriched in newly secreted lipoproteins, while by the time of collection of the late 24 h media extensive remodeling of the secreted lipoproteins has occurred [35, 36, 37, 32]. The longer time has been used in many previous studies of HepG2 lipoprotein secretion [38, 30, 39, 40]. Dimerization of apo A-II and E was blocked at the time of harvest by addition of 5 mM iodoacetamide or 10 mM N-ethyl maleimide (NEM) to alkylate any free cysteines. Medium was collected, centrifuged to pellet cell debris and the supernatant was transferred to fresh tubes. Cell dishes were placed on ice, cells were washed twice with ice-cold PBS, and lysed in NP-40 lysis buffer (50 mM Tris-HCl, 150 mM NaCl, 1% NP-40 (Roche, Indianapolis, IN), pH 8.0) with 10 mM NEM and protease inhibitor cocktail (Roche, Indianapolis, IN). Control experiments showed that this lysis buffer did not affect HDL elution profiles by size exclusion chromatography (data not shown). Cell lysates were centrifuged to remove nuclear debris, and the supernatants transferred to fresh tubes. One-tenth volume 10X buffer (100 mM Tris-HCl pH 7.4, 1 M NaCl, 10 mM EDTA, 10 mM NaN3) was added, and media and lysate samples were stored at 4°C until further processing and analysis.
Lipidated and lipid-free apolipoproteins in cell media were separated essentially as described . Media samples were adjusted to d = 1.25 g/ mL with solid KBr and lipoproteins floated by centrifugation. Three fractions were collected: T: top 3 mL, containing the lipid-associated apolipoproteins; M: middle 3 mL (M); B: bottom 6 mL, containing the lipid-free proteins (B). The middle fraction (M) contained less than 10% of the protein in the bottom (B) fraction and little if any of the lipidated proteins (data not shown). Buffer was exchanged for TBS and samples were concentrated with Centricon Plus-20 centrifugal filter devices, 5,000 MWCO (Millipore, Bedford, MA).
Lipoproteins and lipid-free proteins in media and cell lysate samples were separated by SEC on tandem Superose 6 FPLC columns, as described [41, 42]. Eluants (1 mL) were collected into tubes, which were pooled into 10 fractions each for media and lysate samples, as in Figure 2. Peak elution volumes for human plasma lipoproteins were VLDL, Fraction #1, LDL, Fraction #3 and HDL, Fraction #6; lipid-free apo-A-I eluted in fraction #8. Larger HDL eluted in Fraction 5, and lipid-poor HDL in Fraction 7 .
Columns of Thiopropyl Sepharose 6B (GE Healthcare, Piscataway, NJ), 1 mL bed volume, were used to bind the cysteine containing apo A-II to separate LpA-I from LpA-I/A-II. For study of cell lysates, HepG2 and Huh7 cells, incubated for 2 h in serum-free MEM were lysed as above, except that NEM was omitted, and the lysis buffer pH was adjusted to 7.4, to maintain cytosolic binding conditions. Binding of dimeric apo A-II to TPS requires its prior reduction with DTT to form the free –SH groups to which TPS binds. Thus, lysates were treated with 20 mM DTT to reduce all disulfide bonds and then dialysed against TBS containing 0.5 mM DTT to maintain the reduced –SH groups. The 1mL bed volume minicolumns had a calculated –SH capacity of ~ 15 μmol, corresponding to a 5 fold excess for the amount of DTT to be loaded. The contribution of cell lysate proteins to the total –SH concentration was estimated to be at least an order of magnitude less than that from the 0.5 mM DTT. Human plasma HDL samples were reduced with 20 mM DTT, dialyzed and processed through TPS columns in parallel with the cell lysates as controls for separation of LpA-I from LpA-I/A-II (Figure 4 and Table 2). Four to 6 mL of the reduced and dialyzed cell lysates or HDL were loaded onto the TPS columns. The initial flow-through was recycled through the column for 1 h. The subsequent flow-through was collected (Free fraction), the columns were washed with 5 bed volumes (5 mL) TBS (Wash fraction) and eluted with 5 bed volumes 20 mM DTT in TBS (Bound fraction). Aliquots of each fraction were delipidated, solubilized in SDS-PAGE sample buffer, and analyzed by SDS-PAGE and Western blotting.
To determine the kinetics of LpAI/AII formation in hepatoma media, 60 mL media per time point was collected as above at 0.5, 1.0, 2.0 and 20 h. At the time of harvest, 2 mM paraoxon-ethyl (Sigma, St. Louis) was added to inhibit LCAT to stop further formation of LpAI/AII . After 30 min, 1mM DTT was added to reduce disulfide bonds, and after another 30 min, samples were loaded onto 7 mL bed volume TPS columns. After two passes through the column, the flow through (Free fraction) was collected, the column was washed with 10 bed volumes TBS, and bound fraction was eluted with 5 bed volumes 20 mM DTT in TBS. Free and bound fractions were concentrated and aliquots analyzed by SDS-PAGE and Western blotting.
Lipoproteins and apolipoproteins in media and cell lysates were separated according to density by ultracentrifugation, SEC or TPS and analyzed for apolipoproteins A-I, A-II, B and E by SDS-PAGE (15% Tris-Glycine Ready Gels; BioRad, Hercules, CA) and Western blotting. Samples were loaded in non-reducing or reducing (plus β-mercaptoethanol, (+βMSH)) sample buffer, as indicated in the figure legends. After transfer to nitrocellulose, the Western blotting method was essentially that of the Amersham ECL-Plus Western Blotting Manual (Amersham Biosciences/ GE Healthcare, Piscataway, NJ). Band identification is based on molecular weight and reaction by Western blot with highly specific, high affinity antibodies. All SDS/PAGE gels and Western blots were done with both molecular weight standards and apolipoprotein standards on all the gels/blots. Intensity of bands detected by Western blotting was quantitated either by densitometry of X-ray exposures using Kodak 1D image analysis software, or directly on a Storm 840 imaging system (GE Healthcare, Piscataway, NJ) with ImageQuant TL software. Antibodies for immunoblots were HRP-conjugated goat anti-human apo A-I, apo A-II, apo B and apo E (Academy Biomedical, Houston, TX), or goat polyclonal (Academy Biomedical, Houston, TX) or mouse monoclonal (BioDesign/Meridian Life Sciences, Cincinnati, OH) antibodies with appropriate HRP-conjugated second antibodies (Chemicon/Millipore, Billerica, MA or Jackson Immunoresearch, West Grove, PA).
In our first experiments ultracentrifugation was used to separate lipidated and lipid-free apolipoproteins as previously reported . Immunoblot analysis of fractions from HepG2 cell media harvested after 2 and 24 h (Figure 1; Table 1) demonstrated that at 2 h, apo A-I was partially lipidated (85 %) while apo A-II and apo E were essentially fully lipidated (95%, 94%). Extent of dimerization of apo A-II and apo E was determined by SDS-PAGE analyses under non-reducing and reducing conditions. Most apo A-II in 2 h media is homodimer (92%) while most apo E is monomer (97%). By 24 h, apo E has undergone dimerization (36% A-II-E and 9% E2). At this later time, for all three apolipoproteins, a larger proportion was recovered in the lipid-free d>1.25 fraction (24 – 28%). This could be due to the low amount of lipid production by HepG2 cells [38, 30, 39, 40] and/or loss of apolipoproteins from lipoproteins during ultracentrifugation (see below) [44, 11, 45]. The minor lipid-free apo A-II monomer bands detected in 24 h media (Figure 1, Panel B, anti-A-II, lanes 7 and 8) have increased molecular weight, and may be glycosylated isoforms . All apo B was lipidated at both 2 and 24 h.
Although flotation separates lipidated from lipid-free proteins it provides little information about the lipoprotein subfractions into which apolipoproteins are distributed. To further analyze apolipoprotein lipidation, media and lysates were analyzed by SEC, which resolves lipoprotein particles and lipid-free proteins . Importantly, this method obviates ultracentrifugal artifacts that strip apolipoproteins from HDL [44, 11]. SEC of samples from 2 and 24 h HepG2 media (Figure 2) and the attendant immunoblots of the collected fractions (Figure 3A, 3B) reveal distinct distributions of apolipoproteins A-I, A-II and E. Apo A-I in 2 h media was distributed equally (43% each) between Fractions 6 and 7, which correspond to average plasma-sized HDL and small lipid-poor HDL, with 14% on larger HDL (Fraction 5). By 24 h, media apo A-I on larger HDL increased (Fractions 5 and 6) consistent with maturation of HDL species during the longer incubation time. Essentially all apo A-II in 2 h media is homodimer and most (~69%) elutes in Fraction 6 while 23% elutes on smaller lipid-poor particles (Fraction 7) and 8 % on larger HDL (Fraction 5). At 24 h, Apo A-II homodimer has a lipoprotein distribution like that at 2 h, but the apo A-II-apo E heterodimers formed by this time are on larger HDL (Fractions 4, 5 and 6). Apo E in 2 h media is monomeric, and associated with larger HDL as well as LDL (Fractions 2 – 6). By 24 h, apo E homodimers and apo A-II-apo E heterodimers are detected and these are associated with larger HDL particles (Fractions 4 – 6), while only monomeric apo E is present in LDL Fraction 3. In human plasma also the dimeric apo E content of HDL particles is relatively high while monomeric apo E is predominantly on apo B-containing lipoproteins [29, 45]. Media apo B appeared in Fraction 1 (VLDL) and to a lesser extent in Fraction 3 (LDL) (data not shown).
Cell lysates were harvested at the same time as the 2 and 24 h media, fractionated by SEC and analyzed for apolipoproteins (Figures 2 and 3C, 3D). The distribution of apolipoproteins in the 2 and 24 h lysates differs: the 2 h samples are enriched in newly synthesized intracellular apolipoproteins, while by 24 h the cell lysates contain more lipoproteins that were secreted, processed in the media and endocytosed back into the cell [35, 36]. In 2 h lysates, intracellular apo A-I is 45% lipid-free (Fraction 8), 45% is on small lipid-poor HDL (Fraction 7) and 10% is on average plasma-sized HDL (Fraction 6). In 24 h lysates some apo A-I is on larger LDL sized particles (Figure 3D, Fractions 3 and 4). In 2 h lysates, all apo A-II was dimeric, present as a mix of apo A-II homodimer and A-II-E heterodimer, and eluted in the HDL Fraction 6 (Figure 3C). Thus both dimerization and lipidation of apo A-II occur rapidly after synthesis, prior to secretion. In 24 h lysates, some intracellular apo A-II is in the LDL Fractions 2 – 4 (Figure 3D). Apo E distributed differently among intracellular and secreted lipoproteins. Apo E in 2 h lysates is mostly a monomer in the VLDL Fraction 1 (Figure 3C), whereas in media at 2 and 24 h it is on LDL and large HDL, but no longer detected on VLDL. At 24 h, intracellular apo E is present on VLDL (Fraction 1) and LDL (Fractions 2 – 4), with a small fraction on HDL (Fraction 6). The majority of intracellular apo B in HepG2 cells was in the nascent VLDL fraction (Fraction 1), with a lesser amount in LDL Fractions 2–4 in both the 2 and 24 h lysates (data not shown).
These results clearly demonstrate that apo A-II and apo E lipidation and dimerization follow different, very distinct pathways, and that lipidation of these apolipoproteins both inside hepatocytes and after secretion differs from the lipidation of apo A-I.
Most intracellular apo A-II is lipidated (Figure 3C, Fraction 6) while most apo A-I is lipid-poor (Fraction 7) or lipid-free (Fraction 8), indicating that there is little if any intracellular LpA-I/A-II. To analyze this further, we separated intracellular apo A-I-only particles from apo A-II containing particles by TPS chromatography. As a control, we separated normal human plasma LpA-I and LpA-I/A-II by using TPS (Figure 4, HDL panels). LpA-I flows through the column (Free fraction, lanes 1–3), while LpA-I/A-II binds, and is eluted with 20 mM DTT (Bound fraction, lanes 4 – 6). The relative amounts of apo A-I in the free and bound fractions, 34 + 5% and 66 + 5% (Table 2) agree with published values [8, 1].
TPS analysis of 2 h cell lysates from two different human hepatoma cell lines, HepG2 and Huh7, reveals that essentially all intracellular apo A-I elutes in the flow-through, Free fraction (Figure 4, HepG2 and Huh7 panels, lanes 1 – 3) while all the apo A-II is retained in the Bound fraction (lanes 5 – 7). Quantification of band intensity by phosphorimaging indicates that 98 + 3% and 94 + 9% of the apo A-I in HepG2 and Huh7 cell lysates eluted in the Free fraction, while 99 + 1% and 92 + 11% of the apo A-II was retained in the Bound fraction (Table 2 ). Thus in both HepG2 and Huh7 cells, intracellular apo A-I and apo A-II are present on distinct particles, and do not co-associate on nascent HDL prior to secretion. Rather, as shown below, HDL particles containing both apo A-I and apo A-II (LpA-I/A-II) form after secretion.
TPS analysis of hepatoma cell media reveals a time-dependent increase in secreted apo A-I associated with LpA-I/A-II, with more LpA-I/A-II appearing in the media of HepG2 than in that of Huh7 cells (Figure 5). Immunoblots of the Free and Bound fractions of media collected at 0.5, 1.0, 2.0 and 20 h show apo AI in both fractions, while apo A-II is detectable only in the Bound fractions (Figure 5A). The rate of LpA-I/A-II formation was calculated by quantification of band intensity by phosphorimaging (Figure 5B). LpA-I/A-II formation in hepatoma media is rapid: within 30 min of secretion, 40% of apo A-I in Huh7 media and 73% of apo A-I in HepG2 media is present on LpA-I/A-II. By 20 h, 84% of the apo A-I in HepG2 media and 63% of that in Huh7 media is associated with LpA-I/A-II.
As expected for the cysteine-containing E2 and E3 isoforms, most human plasma HDL apo E is in the bound fraction (Figure 4, lanes 4 – 6 and Table 2). However, a small amount was also found in the free fraction (lanes 1 – 3). In cell lysates, where apo E is present on nascent VLDL (Figure 3C, apo E panel), most apo E was in the bound fractions for both HepG2 and Huh7 cell lysates (Figure 5 and Table 2), but as with HDL apo E, some eluted in the flow-through fractions. The phenotype of HepG2 cell apo E is E3/E3 , one cysteine per protein molecule that should be retained on TPS. However, a fraction of the cysteines in the lipoprotein bound apo E may not be accessible to TPS. After secretion, the amount of apo E in the free fraction decreases with time so that by 20 h all the media apo E binds TPS (Figure 5A and 5C). This change in apo E binding to TPS occurs more rapidly in HepG2 media than in Huh7 media. Changes in apo E conformation on triglyceride rich VLDL that affect receptor binding have been reported .
Our data showing most intracellular apo A-I is lipid-free or on small nascent HDL are consistent with that of others [30, 31, 32, 33, 34]. In elegant pulse-chase studies Chisholm et al reported only 20% of newly synthesized intracellular apo A-I is lipidated prior to secretion, and secretion begins within 30 minutes of synthesis. . We found that in 2 h lysates 45% of intracellular apo A-I was lipid-free, suggesting additional lipidation occurs over this time period. Importantly, in contrast to apo A-I, all intracellular apo A-II and apo E were lipidated within 2 h of synthesis. Although some intracellular apo A-II in 2 h lysates occurred with small, nascent HDL, most was on plasma-sized HDL (Fraction 6, Figure 3C). Most intracellular apo E in 2 h lysates was associated with VLDL. Apo E in rat hepatoma cells has also been reported to bind to maturing VLDL . After secretion, remodeling in the media redistributes the apolipoproteins among lipoproteins; still each apolipoprotein retains a distinctive pattern of lipid association both intracellularly, as we report here for the first time, and post secretion [39, 12]. The patterns of lipid association among apolipoproteins in HepG2 media at 24 h simulate those of human plasma HDL, in which most apo A-II is on mid-size HDL, apo A-I associates with a broader range of particle sizes, and most apo E resides on larger HDL [29, 13].
LpA-I/A-II formation was investigated in two hepatoma cell lines. Though widely used to study lipoprotein secretion, HepG2 cell media apo B-lipoproteins are lipid-poor [38, 30, 39, 40]. In contrast, Huh7 cells [49, 50] are better producers of VLDL [51, 52]. In both cell lines, TPS analysis revealed no detectable intracellular LpA-I/A-II (Figure 4). After secretion, LpA-I/A-II forms rapidly, with faster kinetics in HepG2 than in Huh7 media (Figure 5). Thus, as proposed by Ikewaki et al , LpA-I/A-II forms after secretion of the nascent apo A-II HDL.
The nascent HDL particles secreted by HepG2 cells are discoidal, with low neutral lipids, similar to those found in plasma of LCAT-deficient patients [53, 54] and are remodeled to plasma-like spherical HDL particles by LCAT activity . HepG2 cells secrete many of the proteins and lipids of lipoprotein metabolism, including LCAT, CETP, PLTP and hepatic lipase [38, 56, 57, 58]. Our data confirm the remodeling of secreted lipoproteins to more mature forms in HepG2 media. Apo A-I is hepatically secreted as both lipid-free protein and as lipidated, nascent discoidal HDL particles (this work and [30, 31, 32, 33]). In vitro, these apo A-I particles and model nascent HDL (rHDL) are converted to spherical HDL by LCAT activity [55, 59, 60, 7]. In contrast, discoidal apo A-II rHDL, which are poor LCAT substrates , are not converted to spherical apo A-II HDL [59, 61]. Instead, LCAT catalyzes fusion of the apo A-II rHDL discs with small spherical apo A-I rHDL to form spherical LpA-I/A-II HDL . A similar conversion is observed in vivo; human discoidal apo A-II rHDL infused into rabbits, which lack apo A-II, rapidly fuses with endogenous spherical LpA-I to form LpA-I/A-II . Requirement of LCAT for the in vivo formation of spherical LpA-I/A-II is suggested by the absence of these spherical particles in LCAT deficient patients, where all the apo A-II is confined to pre-β discoidal HDL . Our in vitro data show intracellular apo E is associated with nascent VLDL, while apo E in 2 h media is associated with LDL and HDL. Thus, the apo E on secreted VLDL particles rapidly redistributes to a pattern like that of human plasma .
Lipid-free apo A-II dimerizes slowly, a process that is greatly accelerated by binding to lipids . In HepG2 cells, we found no monomeric intracellular apo A-II, suggesting that following its synthesis apo A-II undergoes rapid, sequential lipidation and dimerization. In contrast, intracellular apo E on VLDL (fraction 1, Figure 3C) is primarily monomeric (this work and ). Apo E dimerization is much slower than that of apo A-II with no dimer detected in media at 2 h, when apo E is associated with LDL and HDL. Apo A-II-apo E heterodimers are present after the longer 24 h incubation, during which lipoprotein remodeling may occur. Apo E is required for HDL remodeling in dog plasma, where it supports the conversion of HDL3 to HDL1, a large, cholesterol-enriched, receptor-competent HDL ; during remodeling, HDL acquire apo E .
Apolipoproteins A-I, A-II and E belong to a gene family of soluble proteins that have amphipathic helical regions that bind to lipids with an affinity, i.e., free energy, that is expected to be apolipoprotein-specific. According to linear free energy relationships, apo A-II homodimerization is expected to increase its free energy of binding by a factor of two. Whereas the free energy of association of monomeric apo A-II with HDL is −7.3 kcal/mol, the corresponding free energy value for dimeric apo A-II is not known and required measuring dimeric lipid-free apo A-II concentrations that were below our level of detection . Our data are consistent with this. Nearly all homo- and heterodimeric apo A-II and apo E are lipidated. In contrast, a greater fraction of monomeric apo A-II and apo E, as well as obligatory monomer apo A-I, are found to be lipid-free after ultracentrifugation (Table 1). The lipid affinities of monomers and dimers may contribute in a currently unknown way to their distinct distributions between lipoproteins species.
Our data are consistent with current models of apo A-I in HDL biogenesis and remodeling [31, 32, 37], and support the following refined model that includes apo A-II and apo E (Figure 6). Synthesis and initial lipidation of apolipoproteins occurs in the endoplasmic reticulum (ER) . Further lipidation occurs in the Golgi, so that half of the apo A-I is secreted on small nascent HDL, while the remainder is secreted as lipid-free apo A-I (Figure 3 and [31, 32]). In contrast, all of apo A-II is lipidated prior to secretion, to a particle size that approaches that of human plasma HDL. Apo A-II is secreted as a lipid-associated dimer on nascent HDL particles that do not contain apo A-I (Figures 3 and and4).4). LCAT catalyzes fusion of the apo A-II nascent HDL discs with small spherical apo A-I HDL to form LpA-I/A-II spherical HDL . Apo E in the Golgi associates with maturing VLDL particles (Figure 3 and ). Apo E secreted on VLDL is rapidly remodeled (double arrow) into LDL-sized particles and moves to HDL, where it subsequently forms homodimers and heterodimers with apo A-II. These secreted lipoproteins may undergo retroendocytosis, after which some apo A-I and apo A-II transfer to LDL-sized particles, while apo E transfers to HDL and is resecreted [37, 36].
The unique distributions of apolipoproteins A-I, A-II and E among nascent and maturing lipoprotein particles suggest apolipoprotein-specific HDL formation and processing. Lipidated and lipid-free apo A-I are expected to support cellular cholesterol efflux via ABCG1 and ABCA1 respectively [32, 65, 66], and if HepG2 and Huh7 cells are valid models of hepatocytes in vivo, one could surmise that lipid-free apo A-I is rapidly utilized by ABCA1 or renally disposed because plasma lipid-free apo A-I concentrations are very low (<0.05%) . Lp A-I/A-II are formed by the LCAT promoted fusion of small spherical apo A-I HDL with nascent discoidal apo A-II-HDL [7, 10]. Whereas plasma levels of apo A-I are determined by catabolism, apo A-II levels are determined by synthetic rate. This is a major factor regulating the distribution of apo A-I among HDL subclasses LpA-I and LpA-I/A-II in normolipidemic humans [67, 8]. Plasma residence time for apo A-II is longer than that for apo AI , consistent with its higher lipophilicity, and with the lability of apo A-I association with HDL [41, 69, 42, 2]. Apo A-II also modulates the substrate properties of HDL. The rate of hepatic lipase catalyzed fatty acid release from HDL containing apo A-II is twice that of HDL devoid of apo A-II . Apo E HDL also have distinct properties; apo E facilitates RCT by allowing CE-rich-core expansion of HDL . Understanding the roles of apolipoprotein-specific HDL metabolism will provide the basis for development of better therapies to promote RCT.
This work was supported by grants-in-aid from the National Institutes of Health HL-30914 and HL-56865 to H.J.P. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Heart Lung and Blood Institute nor the National Institutes of Health. We thank Amber Chen for technical assistance, Dr. Dan Liao for bringing to our attention the human hepatoma Huh7 cell line, and Dr. Yumin Xu in Dr. Boris Yoffe’s laboratory (Baylor College of Medicine) for giving us a flask of these cells.
Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.