Open Access

Proprotein convertases in high-density lipoprotein metabolism

Biomarker Research20131:27

https://doi.org/10.1186/2050-7771-1-27

Received: 23 July 2013

Accepted: 4 September 2013

Published: 18 September 2013

Abstract

The proprotein convertase subtilisin/kexins (PCSKs) are a serine endopeptidase family. PCSK members cleave amino acid residues and modulate the activity of precursor proteins. Evidence from patients and animal models carrying genetic alterations in PCSK members show that PCSK members are involved in various metabolic processes. These studies further revealed the molecular mechanism by which genetic alteration of some PCSK members impairs normal molecular and physiological functions, which in turn lead to cardiovascular disease. High-density lipoprotein (HDL) is anti-atherogenic as it removes excessive amount of cholesterol from blood and peripheral tissues. Several PCSK members are involved in HDL metabolism. PCSK3, PCSK5, and PCSK6 process two triglyceride lipase family members, endothelial lipase and lipoprotein lipase, which are important for HDL remodeling. Recent studies in our lab found evidence that PCSK1 and PCSK9 are also involved in HDL metabolism. A mouse model carrying an amino acid substitution in PCSK1 showed an increase in serum apolipoprotein A1 (APOA1) level. Another mouse model lacking PCSK9 showed a decrease in APOE-containing HDL. In this review, we summarize the role of the five PCSK members in lipid, glucose, and bile acid (BA) metabolism, each of which can influence HDL metabolism. We propose an integrative model in which PCSK members regulate HDL metabolism through various molecular mechanisms and metabolic processes and genetic variation in some PCSK members may affect the efficiency of reverse cholesterol transport. PCSK members are considered as attractive therapeutic targets. A greater understanding of the molecular and physiological functions of PCSK members will improve therapeutic strategies and drug efficacy for cardiovascular disease where PCSK members play critical role, with fewer adverse effects.

Keywords

Proprotein convertase subtilisin/kexin High-density lipoprotein cholesterol Reverse cholesterol transport

Introduction

In the past two decades nine members of the highly conserved bacterial subtilisin- and yeast kexin-like serine protease family have been discovered and characterized. Analyses in animal models and in patients with mutations in PCSK members have revealed the molecular mechanism by which genetic alterations in PCSK members affect molecular and physiological functions in various metabolic diseases and endocrinological defects [14]. However, our understanding of how PCSK members are involved in HDL metabolism is still limited. The HDL biology has been updated in many reviews during the past decades [510], and we briefly summarize several key points: The major function of HDL is to remove excessive amounts of cholesterol from peripheral tissues via a mechanism called reverse cholesterol transport (RCT). HDL takes up cholesterol from low-density lipoprotein (LDL) or macrophage foam cells in atherosclerotic lesions and then delivers it to the liver for recycling or excretion. As a high level of HDL correlates with low risk of atherosclerotic cardiovascular diseases, HDL is considered an anti-atherogenic factor. Thus, abnormal regulation of HDL synthesis, remodeling and catabolism causes reduced HDL cholesterol concentration and HDL function, which then promotes the risk or progression of the disease.

Some PCSK members were previously found to be important in HDL metabolism. Data from our lab shows that PCSK1 is involved in regulating the levels of serum apolipoprotein A1 (APOA1), which is the major protein for HDL formation and remodeling (Choi et al., in preparation). PCSK3, PCSK5 and PCSK6 process two members in the triglyceride (TG) lipase family: endothelial lipases (EL) and lipoprotein lipases (LPL) [11] that play important role in regulating the HDL cholesterol concentration. We have also shown that PCSK9 influences HDL cholesterol concentration by regulating APOE-containing HDL levels [12].

Protein structure and principle of PCSK

PCSK proteins consist of several peptide domains: a signal peptide/transmembrane domain at the amino-terminus, a prosegment domain, a catalytic domain, a P domain, a Cys-rich domain, a cytoplasmic tail, and a Cys-His-rich domain at the carboxyl-terminus [1]. The catalytic domain is the most conserved sequence and the identity is about 35% and the presence of first three domains is common between the five PCSK members (Figure 1). The PCSK family consists of two groups divided by amino acid cleavage sites: typical and atypical (Table 1) [13]. PCSK1, PCSK3, PCSK5, and PCSK6 are typical members and cleave single or paired basic amino acids with the motif (R/K)X n (R/K)↓, where the arrow indicates the cleavage site and X n corresponds to a 0-, 2-, 4-, or 6-amino-acid spacer [2]. PCSK9 is an atypical member and cleaves non-basic residues at the C-terminal end of the motif RX(L/V/I)X↓, where X represents any amino acid except for cysteine and proline [14]. PCSK9 cleaves itself at its internal (V/I/L)FAQ152↓ sequence, and then acts as a binding protein for cell surface receptors [15, 16].
Figure 1

Schematic illustration for the protein structure; typical and atypical cleavage activies of human PCSK1, PCSK3, PCSK5, PCSK6, and PCSK9. The figure illustrates the peptide domains and cleavage site of human PCSK1, PCSK3, PCSK5, PCSK6, and PCSK9. The five PCSK members consist of several peptide domains: a signal peptide/transmembrane domain (S/T) at the amino-terminus, a pro-segment domain (Pro), a catalytic domain (Cat), a P domain (P), a Cys-rich domain (Cys), a cytoplasmic tail (Cyt), and a Cys-His-rich domain (CHRD) at the carboxyl-terminus. Three protein domains are common between five PCSK members: S/T, Pro, and Cat domains. Typical members (PCSK1, PCSK3, PCSK5, and PCSK6) cleaves single or paired basic amino acids with the motif (R/K)X n (R/K)↓, where the arrow indicates the cleavage site and X n corresponds to a 0-, 2-, 4-, or 6-amino-acid spacer at (R/K)X n (R/K)↓, meanwhile atypical member (PCSK9) cleaves non-basic residues at the C-terminal end of the motif (V/I/L)FAQ↓.

Table 1

Official and alternative protein name of the nine PCSK members

Member type

Official name

Alternative name

Typical

PCSK1

PCSK1

PCSK2

PCSK2

FURIN

PCSK3

PCSK4

PCSK4

PCSK5

PCSK5

PCSK6

PCSK6

PCSK7

PCSK7

Atypical

MBTPS1*

PCSK8

 

PCSK9

PCSK9

•MBTPS1: membrane-bound transcription factor peptidase, site 1.

PCSKs and lipid metabolism

Some PCSK members are involved in regulating the activity of important modulators of lipid metabolism (Figure2A) [3]. The potential role for PCSK1 in lipid metabolism was observed in a study using a loss-of-functional mouse model that carries a mutation in Pcsk1 (Choi et al., in preparation). The mutation was introduced by treating mice with N-ethyl-N-nitrosourea (ENU), a chemical that induces A- > G transition, which led to an amino acid substitution from asparagine (N) to aspartic acid (D) at position 222. The mutation reduces enzymatic activity of PCSK1 in cleaving downstream substrates [17, 18]. In the PCSK1 mutant male mice on a chow-diet for 8 weeks, serum apolipoprotein A1 (APOA1), which is the major component of HDL, was 1.5-2.0 fold increased (Figure 2A(1)), but fasting serum HDL cholesterol concentration in the PCSK1 mutant was similar to wild-type controls. In the PCSK1 mutant mouse livers, APOA1 concentration was ~2.0 fold decreased, while Apoa1 expression was similar, suggesting that PCSK1 is involved in regulating serum APOA1 concentration and that PCSK1 mutant might increase APOA1 secretion from the liver to serum. It is still unknown why HDL cholesterol concentration is not effected despite the increase in APOA1.
Figure 2

The role of PCSK members in various metabolic processes and disorders. The figure illustrates the role of PCSK1, PCSK3, PCSK5, PCSK6, and PCSK9 in lipid (A), glucose (B), and BA (C) metabolism. Arrows with 2 different types of lines indicate the relationship between factors: solid lines with arrow indicate a “positive influence” and dotted lines with arrow indicate a “negative influence.” For example, PCSK3, 5, and 6 inactivates EL (Figure 2A(2)). In contrast, solid lines with arrow indicate a “positive influence.” For example, PCSK9 inhibition decreases serum APOB level (Figure 2(5)).

PCSK3, PCSK5, and PCSK6 are involved in lipid metabolism by modulating two members of the TG lipase family. The three PCSK members negatively influences EL activity by cleaving a carboxyl-terminal 18 kDa fragment in EL to suppress the enzymatic activity of EL (Figure 2A(2)) [19]. EL cleavage was induced by transient expression of PCSK3, PCSK5, and PCSK6 in HEK293 cells [20]. PCSK3 may also negatively influence EL activity through angiopoeitin-like protein 3 (ANGPTL3) (Figure 2A(3)). Adenoviral transduction of PCSK3 in hepatocytes led to less cleavage product and increased full-length ANGPTL3 [11]. ANGPTL3 inhibited ~60% of EL activity by transfecting a plasmid expressing murine ANGPTL3 into HEK293 cells stably expressing EL [11]. Lipoprotein lipase (LPL) is another member of the TG lipase family that is similarly inactivated by PCSK-mediated proteolytic cleavage (Figure 2A(4)) [21]. Transient expression of PCSK3, PCSK5, and PCSK6 induced LPL cleavage in HEK293 cells [20].

The first work that linked PCSK9 with lipid metabolism was published by Abifadel and colleagues 10 years ago. Gain-of-function mutations in PCSK9 were found in familial autosomal dominant hypercholesterolemia patients [22]. The mutations increase LDLR degradation and decrease LDL clearance, which results in an increase in circulating LDL. PCSK9 positively regulates APOB concentration (Figure 2(5)) and inhibition of PCSK9 leads to an increase of LDLR (Figure 2A(6)) and APOB-containing LDL particles are more rapidly cleared. PCSK9 also promotes degradation of the VLDL receptor (VLDLR) and APOE receptor type 2 (LRP8), both of which are important in TG and VLDL metabolism. PCSK9 negatively regulates VLDL concentration through the two receptors (Figure 2A(7)). Ectopic expression of the PCSK9 gene in HEK293 cells reduced the levels of LRP8 and VLDLR, while PCSK9 inhibition in CHO-1 and HEK293 cell lines increased the levels of VLDLR [23].

PCSKs and glucose metabolism

PCSK1 and PCSK9 are involved in glucose metabolism (Figure 2B) [1]. PCSK1 and PCSK9 positively regulate pro-insulin conversion to insulin by proteolytic cleavage in the pancreas. A non-synonymous single nucleotide polymorphism in human PCSK1 (rs6232) substitutes asparagine with aspartic acid at codon 221 (N221D). Transfecting recombinant N221D PCSK1 protein in human embryonic kidney 293 cells reduces the proteolytic cleavage of its substrate [24]. The rs6232 variant is associated with an increase in fasting blood glucose level and a decrease in pancreatic β-cell function and insulin resistance [25]. Insulin was decreased in the pancreas of PCSK9 KO C57BL/6 males, and the males exhibited hyperinsulinemic, hyperglycemic, and glucose-intolerant phenotypes [26].

PCSKs and BA metabolism

PCSK1 and PCSK5 are involved in BA metabolism (Figure 2C) and positively regulate CCK in the small intestine by converting procholecystokinin (proCCK) to CCK [27]. An immunohistochemical analysis and an in vitro cleavage assay showed that PCSK1 co-localizes with proCCK and positively regulates proCCK level. The uncleaved proCCK level was increased and the cleaved CCK level was decreased in the small intestine of mice lacking PCSK1 compared to wild-type control mice [28]. Treating cultured mouse small intestinal cells with small-interfering (si) RNA against Pcsk5 significantly reduced the secretion of cleaved CCK into the cell culture medium [29]. The secretion of CCK from the small intestine stimulates BA secretion from the gall bladder to the gut. BAs promote lipid absorption and modulate cholesterol levels through enterohepatic circulation. Defects in BA metabolism cause jaundice of the eye and skin.

PCSKs and HDL metabolism

PCSK3, PCSK5, and PCSK6 are involved in HDL metabolism by modulating EL and LPL. EL is expressed on the surface of vascular endothelial cells and hydrolyzes phospholipids in HDL. Over-expression of EL in mice leads to a decrease in HDL cholesterol concentration while mice lacking EL show elevated HDL cholesterol concentration (Figure 3(1)) [30]. LPL activation by treating rats with LPL inducing reagent (NO-1886) increased HDL cholesterol concentration [31], showing that LPL activity positively correlates with serum HDL cholesterol concentration (Figure 3(2)). Recent animal studies, including ours, showed that PCSK9 is involved in HDL metabolism. PCSK9 KO male mice on a C57BL/6 background and fed a chow diet exhibited a 30% reduction of HDL cholesterol concentrations [32]. C57BL/6 males fed a high fat diet and then treated with a Pcsk9 antisense oligonucleotide inhibitor for 6 weeks showed a 54% reduction in HDL cholesterol concentration [33]. In male cynomolgus macaques, treatment with neutralizing antibodies against PCSK9 reduced HDL cholesterol concentrations for the first seven days of treatment [34]. Data from our lab shows the molecular mechanism in which PCSK9-mediated HDL regulation is mainly through low-density lipoprotein (LDLR) [12]. PCSK9 inhibition increases LDLR level, suggesting the negative relationship between PCSK9 and LDLR (Figure 3(3)). Increased LDLR subsequently induces the binding of LDLR to APOE in HDL and thereby leads to rapid HDL clearance. In mice, HDL is the primary cholesterol carrier and the majority of cholesterol is enriched in APOE-containing HDL particles so that reduced level of APOE-containing HDL in the PCSK9 KO mice is likely to be a cause of reduced HDL cholesterol concentration. Thus, LDLR negatively influences HDL cholesterol concentration (Figure 3(4)).
Figure 3

Integrated physiological model of the molecular and metabolic networking between PCSK members. The figure illustrates the role of PCSK1, PCSK3, PCSK5, PCSK6, and PCSK9 in the lipoprotein triad (HDL, LDL and VLDL). HDL level and function are synergistically regulated by those metabolic factors: glucose, triglyceride (TG) and BA metabolism. Arrows with 2 different types of lines indicate the relationship between factors: dotted lines with arrow indicate a “negative influence.” For example, LDLR decreases HDL cholesterol concentration (Figure 3(4)). In contrast, solid lines with arrow indicate a “positive influence.” For example, CCK secreted from the small intestine stimulates BA secretion (Figure 3(5)). Solid lines without arrow indicate two major ways of reverse cholesterol transport (RCT). First, cholesteryl ester transfer protein (CETP) exchanges cholesterol in LDL by TG in HDL (Figure 3(9)). Second, HDL takes up cholesterol that is accumulated in macrophage foam cells inside the blood vessel wall (Figure 3(10)). Cholesterol-carrying HDL returns to the liver to recycle or excrete the cholesterol.

Normal regulation of insulin, glucose, hormones, and lipids is important for HDL homeostasis, which involves synthesis, action, and elimination of HDL lipoproteins [35, 36]. Mutations in PCSK1 and PCSK5 may cause abnormal HDL metabolism through mis-regulation of signal molecules in BA. For example, CCK or chenodeoxycholic acid (CDCA) positively influences BA metabolism (Figure 3(5)). When dietary lipids and other nutrients arrive in the gut, cholecystokinin (CCK) secreted from the small intestine stimulates BA secretion from the gall bladder to the gut. The majority of the BA is re-absorbed into the liver via enterohepatic circulation and the reminder is excreted through feces. CDCA is a major component in the BA and functions as a signaling molecule in HDL metabolism. CDCA binds to the farnesoid X-activated receptor (FXR) that regulates lipid and cholesterol metabolism [37]. FXR, a member of the nuclear hormone receptor superfamily, forms a heterodimer with the retinoid X receptor (RXR). The FXR/RXR heterodimer functions as a transcription factor that positively influences phospholipid transfer protein (PLTP) mRNA transcription (Figure 3(6)). Co-transfecting FXR and RXR expression plasmids and CDCA treatment in monkey kidney cells increased PLTP promoter activity. Cholic acid, another major component in the BA, is involved in PLTP regulation [38]. Mice fed a chow diet with cholic acid exhibited increased hepatic PLTP mRNA levels. PLTP is an important factor for HDL conversion and positively influence HDL level (Figure 3(7)). Mice lacking the Pltp gene displayed reduced levels of HDL cholesterol (65%) and APOA1 protein (85%) (Figure 3(8)) compared to wild-type control mice [39]. In humans, a non-synonymous mutation of L196W in the PLTP gene impairs HDL conversion [40, 41].

Maintenance of normal HDL metabolism is critical for normal physiological function of HDL. Reverse cholesterol transport (RCT) is an anti-atherogenic process that occurs between lipoproteins (Figure 3(9)) or between lipoproteins and macrophage foam cells (Figure 3(10)). The efficiency of RCT can be analyzed by measuring the amount of cholesterol in medium and cells. EL deficiency affects efficiency of cholesterol efflux from macrophages. EL knockdown using small hairpin (sh) RNA reduced APOA1-mediated cholesterol efflux [42]. PCSK9 KO decreases the efficiency of cholesterol efflux [12]. Treating PCSK9 KO mouse serum to cultured macrophage foam cells exhibits decreased cholesterol efflux. Thus, abnormal HDL regulation caused by genetic alterations in some PCSK members may interfere with reverse cholesterol transport efficiency.

Normal insulin processing, which influences glucose and triglyceride metabolism, is critical for maintaining normal HDL metabolism [35]. Type II diabetic patients show decreased small HDL particles [43]. Hypertriglyceridemia patients with hyperglycemic phenotype exhibited increased TG-rich HDL with lower stability and shorter plasma residence time compare to cholesterol-rich HDL (Figure 2(11)) [44]. The TG-rich HDL is rapidly catabolized, which subsequently decreases plasma HDL cholesterol concentration [45]. Another potential cause of abnormal HDL metabolism is glycation that leads to conformation changes of proteins. Glycation of amino-acid residues in APOA1 alters its binding affinity to ATP-binding cassette sub-family G member 1 (ABCG1) in the human acute monocytic leukemia cell lines (THP-1). As a result, the ability of cholesterol efflux from THP-1 cells was significantly reduced (< 70%) compared to unglycated APOA1 [46].

Conclusion and discussion

In this review, we summarize how PCSK1, 3, 5, 6, and 9 influence HDL cholesterol concentrations by regulating modulators in various metabolic processes (Figure 4). We also review the current understanding of how five PCSK members are linked not only to abnormal HDL metabolism, but also to other metabolic processes including regulation of lipid, glucose, and BA. To explain the complex relationships between the PCSK members and various metabolic processes, an integrated physiological point of view will be critical to improve our understanding about PCSK members. We propose a model in which PCSK members play pivotal roles in HDL, non-HDL, glucose, insulin, BA, and TG regulation. For example, PCSK1 influences lipoprotein, glucose, and BA metabolism by regulating APOA1, the activity of insulin, and CCK. PCSK3 and PCSK5 influence lipoprotein metabolism by modulating the activity of EL, LPL, and the level of LDLR through PCSK9 cleavage. PCSK9 influences glucose and lipoprotein metabolisms by regulating insulin and LDLR receptor degradation.
Figure 4

The role and action of PCSK members in regulating HDL cholesterol concentration. The figure illustrates the role and action of PCSK1, PCSK3, PCSK5, PCSK6, and PCSK9 in HDL cholesterol concentration. Arrows with 2 different types of lines indicate the relationship between factors: solid lines with arrow indicate a “positive influence” and dotted line with arrow indicates a “negative influence.” Solid line without arrow indicates a “no influence.” PCSK1 negatively influences serum APOA1 level, but does not influence HDL cholesterol concentration, PCSK3, 5 and 6 positively influences HDL cholesterol concentration by modulating enzymatic activities of EL and LPL. PCSK9 positively influences HDL cholesterol concentration by regulating APOE-containing HDL subfraction level through LDLR.

Some of the PCSK members have functional redundancy by processing common substrates: insulin by PCSK1 and PCSK9; CCK by PCSK1 and PCSK5; TG lipases (EL and LPL) by PCSK3, PCSK5, and PCSK6. In the latter case, all 3 PCSKs modulate the activity of the TG lipases, but the efficiency of the modulation varies: for EL inactivation PCSK6 has the highest efficiency while PCSK3 has the lowest efficiency; for LPL activation PCSK3 has the highest efficiency while PCSK5 has the lowest efficiency [11]. The PCSK members also regulate one another. The activity of PCSK9 is negatively influenced by two other PCSK members: PCSK3 (Figure 3(12)) and PCSK5 (Figure 3(13)). PCSK3 cleaves PCSK9 at the Arg218-Gln219 peptide bond in HEK293 cells, and PCSK5 cleaves the same bond, but with lower efficiency compared to PCSK3 [11].

The biology and therapeutic targeting of PCSK members has been recently reviewed [1]. Particularly, therapeutic inhibition of PCSK9 has been proven to be a promising pro-atherogenic LDL cholesterol-lowering treatment. Co-treatment of PCSK inhibitors with drugs that suppress cholesterol synthesis is even more effective in reducing LDL cholesterol in hypercholesterolemia patients [47]. Also, PCSK9 inhibition in the patients did not cause negative impact on anti-atherognic HDL cholesterol concentration in early-phase clinical trial phase I or phase II [4749]. However, the effect of PCSK9 inhibition on HDL cholesterol concentration is controversial. Some studies used mice showed that PCSK9 inhibition decreases HDL cholesterol concentration [12, 32]. Because HDL cholesterol regulation and metabolism differ between mouse and human, we speculate that in human, although the inhibition of PCSK9 affects LDLR level, it might not cause strong enough effect to see significant measurable impact on HDL cholesterol concentration. In humans, cholesterol ester transfer protein (CETP) is a critical factor for regulating HDL cholesterol concentration by transferring cholesterol from HDL to non-HDL particles. In mice lacking CETP, cholesterol is enriched in APOE-containing HDL particles and the particles are cleared through LDLR. In other words, the effect of an increase of LDLR level by PCSK9 inhibition on HDL cholesterol concentration in humans might be smaller relative to its effect in mice. At the same time, studies in nonhuman primates, which have CETP and have similar HDL cholesterol metabolism to humans in comparison to mice, show inconsistent results in regards to the effect of PCSK9 inhibition on HDL cholesterol concentration [34, 50]. Treatment with neutralizing antibody against PCSK9 for the first 7 days of treatment decreased HDL cholesterol concentration [34]. Meanwhile, knockdown of PCSK9 by RNAi did not decrease HDL cholesterol concentration [50]. The data from these studies suggest that there are likely to be other factors causing the inconsistent results between studies. First, it is possible that the inconsistent results between studies might be caused by the dosage of PCSK9 inhibition. Knockout of PCSK9 in mice [12, 32] decreased HDL cholesterol concentrations and knockdown of PCSK9 by RNAi [50] and overexpression of PCSK9 by adenovirus [51] did not decrease HDL cholesterol concentrations. Second, it is also possible that whether or not PCSK9 targeting directs liver might cause the inconsistent results. Liver-specific siRNA silencing [50] and overexpression of PCSK9 by adenovirus, which is known to primarily target the liver, do not decrease HDL cholesterol concentration. PCSK9 in other tissues remains unaffected and might contribute to the lack of decreased HDL cholesterol concentration. The no change in HDL cholesterol concentration despite the change in LDLR by PCSK9 inhibition [50] and overexpression [51] remains unclear and additional studies would be needed to address this observation. If the method is indeed the cause of the variation in HDL cholesterol, then additional studies may provide valuable information about the effectiveness of different methods. At the same time, the use of neutralizing antibodies against PCSK9 in several clinical trials [4749] show no negative impact on HDL cholesterol concentration. Considering the importance of PCSK9 as a promising therapeutic target, it will be important to understand whether the inconsistent results are due to different dosage (knockout versus knockdown), CETP (presence vs absence), or target (gene vs protein; liver vs organism). The molecular and physiological functions of PCSK members in HDL metabolism are likely more complex than we currently know. In particular, our understanding of compensatory mechanisms between PCSK members is also limited. We look forward to continued studies that will improve our understanding and allow more precise pharmacological regulation of PCSK for the treatment of metabolic disease.

Authors’ information

SC: Ph.D. candidate in the cooperative pre-doctoral program at The Jackson Laboratory, Bar Harbor, ME 40609, USA. RK: assistant professor at the Jackson Laboratory and adjunct research scientist at The Mount Desert Island Biological Laboratory, Bar Harbor, ME 04609, USA.

Declarations

Acknowledgments

This work was supported by HL081162, HL077796, and HL095668 from the National Heart, Lung and Blood Institute. The authors thank Dr. Xiaosong Wang for critical review of the manuscript; Joanne Currer, Kyle Beauchemin, Elisabeth Adkins, Aleksandra Aljakna, and George Sutphin for manuscript preparation.

Authors’ Affiliations

(1)
The Jackson Laboratory
(2)
Graduate School of Biomedical Sciences, University of Maine

References

  1. Seidah NG, Prat A: The biology and therapeutic targeting of the proprotein convertases. Nat rev Drug discov 2012, 11: 367–383. 10.1038/nrd3699PubMedView ArticleGoogle Scholar
  2. Seidah NG, Chretien M: Proprotein and prohormone convertases: a family of subtilases generating diverse bioactive polypeptides. Brain Res 1999, 848: 45–62. 10.1016/S0006-8993(99)01909-5PubMedView ArticleGoogle Scholar
  3. Seidah NG, Khatib AM, Prat A: The proprotein convertases and their implication in sterol and/or lipid metabolism. Biol Chem 2006, 387: 871–877.PubMedView ArticleGoogle Scholar
  4. Seidah NG, Mayer G, Zaid A, Rousselet E, Nassoury N, Poirier S, Essalmani R, Prat A: The activation and physiological functions of the proprotein convertases. Int J Biochem Cell Biol 2008, 40: 1111–1125. 10.1016/j.biocel.2008.01.030PubMedView ArticleGoogle Scholar
  5. Pownall HJ, Morrisett JD, Sparrow JT, Smith LC, Shepherd J, Jackson RL, Gotto AM Jr: A review of the unique features of HDL apoproteins. Lipids 1979, 14: 428–434. 10.1007/BF02533429PubMedView ArticleGoogle Scholar
  6. Boes E, Coassin S, Kollerits B, Heid IM, Kronenberg F: Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review. Exp Gerontol 2009, 44: 136–160. 10.1016/j.exger.2008.11.003PubMed CentralPubMedView ArticleGoogle Scholar
  7. Rader DJ: Mechanisms of disease: HDL metabolism as a target for novel therapies. Nat Clin Pract Cardiovasc Med 2007, 4: 102–109. 10.1038/ncpcardio0768PubMedView ArticleGoogle Scholar
  8. Rader DJ: Molecular regulation of HDL metabolism and function: implications for novel therapies. The J clin investig 2006, 116: 3090–3100. 10.1172/JCI30163PubMedView ArticleGoogle Scholar
  9. Lewis GF, Rader DJ: New insights into the regulation of HDL metabolism and reverse cholesterol transport. Circ Res 2005, 96: 1221–1232. 10.1161/01.RES.0000170946.56981.5cPubMedView ArticleGoogle Scholar
  10. Brewer HB Jr, Rader DJ: HDL: structure, function and metabolism. Prog in lipid res 1991, 30: 139–144. 10.1016/0163-7827(91)90009-TView ArticleGoogle Scholar
  11. Jin W, Wang X, Millar JS, Quertermous T, Rothblat GH, Glick JM, Rader DJ: Hepatic proprotein convertases modulate HDL metabolism. Cell Metab 2007, 6: 129–136. 10.1016/j.cmet.2007.07.009PubMed CentralPubMedView ArticleGoogle Scholar
  12. Choi S, Aljakna A, Srivastava U, Peterson BR, Deng B, Prat A, Korstanje R: Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9. Lipids Health Dis 2013, 12: 112. 10.1186/1476-511X-12-112PubMed CentralPubMedView ArticleGoogle Scholar
  13. Seidah NG, Chretien M, Day R: The family of subtilisin/kexin like pro-protein and pro-hormone convertases: divergent or shared functions. Biochimie 1994, 76: 197–209. 10.1016/0300-9084(94)90147-3PubMedView ArticleGoogle Scholar
  14. Pasquato A, Pullikotil P, Asselin MC, Vacatello M, Paolillo L, Ghezzo F, Basso F, Di Bello C, Dettin M, Seidah NG: The proprotein convertase SKI-1/S1P. In vitro analysis of Lassa virus glycoprotein-derived substrates and ex vivo validation of irreversible peptide inhibitors. J Biol Chem 2006, 281: 23471–23481. 10.1074/jbc.M513675200PubMedView ArticleGoogle Scholar
  15. Naureckiene S, Ma L, Sreekumar K, Purandare U, Lo CF, Huang Y, Chiang LW, Grenier JM, Ozenberger BA, Jacobsen JS, et al.: Functional characterization of narc 1, a novel proteinase related to proteinase K. Arch Biochem Biophys 2003, 420: 55–67. 10.1016/j.abb.2003.09.011PubMedView ArticleGoogle Scholar
  16. Benjannet S, Rhainds D, Essalmani R, Mayne J, Wickham L, Jin W, Asselin MC, Hamelin J, Varret M, Allard D, et al.: NARC-1/PCSK9 and its natural mutants: zymogen cleavage and effects on the low density lipoprotein (LDL) receptor and LDL cholesterol. J Biol Chem 2004, 279: 48865–48875. 10.1074/jbc.M409699200PubMedView ArticleGoogle Scholar
  17. Lloyd DJ, Bohan S, Gekakis N: Obesity, hyperphagia and increased metabolic efficiency in Pc1 mutant mice. Hum Mol Genet 2006, 15: 1884–1893. 10.1093/hmg/ddl111PubMedView ArticleGoogle Scholar
  18. Pickett LA, Yourshaw M, Albornoz V, Chen Z, Solorzano-Vargas RS, Nelson SF, Martin MG, Lindberg I: Functional consequences of a novel variant of PCSK1. PLoS One 2013, 8: e55065. 10.1371/journal.pone.0055065PubMed CentralPubMedView ArticleGoogle Scholar
  19. Gauster M, Hrzenjak A, Schick K, Frank S: Endothelial lipase is inactivated upon cleavage by the members of the proprotein convertase family. J Lipid Res 2005, 46: 977–987. 10.1194/jlr.M400500-JLR200PubMedView ArticleGoogle Scholar
  20. Jin W, Fuki IV, Seidah NG, Benjannet S, Glick JM, Rader DJ: Proprotein convertases [corrected] are responsible for proteolysis and inactivation of endothelial lipase. J Biol Chem 2005, 280: 36551–36559. 10.1074/jbc.M502264200PubMedView ArticleGoogle Scholar
  21. Liu J, Afroza H, Rader DJ, Jin W: Angiopoietin-like protein 3 inhibits lipoprotein lipase activity through enhancing its cleavage by proprotein convertases. J Biol Chem 2010, 285: 27561–27570. 10.1074/jbc.M110.144279PubMed CentralPubMedView ArticleGoogle Scholar
  22. Abifadel M, Varret M, Rabes JP, Allard D, Ouguerram K, Devillers M, Cruaud C, Benjannet S, Wickham L, Erlich D, et al.: Mutations in PCSK9 cause autosomal dominant hypercholesterolemia. Nat Genet 2003, 34: 154–156. 10.1038/ng1161PubMedView ArticleGoogle Scholar
  23. Poirier S, Mayer G, Benjannet S, Bergeron E, Marcinkiewicz J, Nassoury N, Mayer H, Nimpf J, Prat A, Seidah NG: The proprotein convertase PCSK9 induces the degradation of low density lipoprotein receptor (LDLR) and its closest family members VLDLR and ApoER2. J Biol Chem 2008, 283: 2363–2372.PubMedView ArticleGoogle Scholar
  24. Benzinou M, Creemers JW, Choquet H, Lobbens S, Dina C, Durand E, Guerardel A, Boutin P, Jouret B, Heude B, et al.: Common nonsynonymous variants in PCSK1 confer risk of obesity. Nat Genet 2008, 40: 943–945. 10.1038/ng.177PubMedView ArticleGoogle Scholar
  25. Heni M, Haupt A, Schafer SA, Ketterer C, Thamer C, Machicao F, Stefan N, Staiger H, Haring HU, Fritsche A: Association of obesity risk SNPs in PCSK1 with insulin sensitivity and proinsulin conversion. BMC Med Genet 2010, 11: 86.PubMed CentralPubMedView ArticleGoogle Scholar
  26. Mbikay M, Sirois F, Mayne J, Wang GS, Chen A, Dewpura T, Prat A, Seidah NG, Chretien M, Scott FW: PCSK9-Deficient mice exhibit impaired glucose tolerance and pancreatic islet abnormalities. FEBS Lett 2010, 584: 701–706. 10.1016/j.febslet.2009.12.018PubMedView ArticleGoogle Scholar
  27. Gagnon J, Mayne J, Mbikay M, Woulfe J, Chretien M: Expression of PCSK1 (PC1/3), PCSK2 (PC2) and PCSK3 (furin) in mouse small intestine. Regul Pept 2009, 152: 54–60. 10.1016/j.regpep.2008.07.006PubMedView ArticleGoogle Scholar
  28. Rehfeld JF, Bundgaard JR, Hannibal J, Zhu X, Norrbom C, Steiner DF, Friis-Hansen L: The cell-specific pattern of cholecystokinin peptides in endocrine cells versus neurons is governed by the expression of prohormone convertases 1/3, 2, and 5/6. Endocrinology 2008, 149: 1600–1608. 10.1210/en.2007-0278PubMed CentralPubMedView ArticleGoogle Scholar
  29. Reynolds NA, Blum A, Kitagawa K, Beinfeld MC: Inhibition of PC5 expression decreases CCK secretion and increases PC2 expression. Peptides 2006, 27: 901–904. 10.1016/j.peptides.2005.09.010PubMedView ArticleGoogle Scholar
  30. Cilingiroglu M, Ballantyne C: Endothelial lipase and cholesterol metabolism. Curr Atheroscler Rep 2004, 6: 126–130. 10.1007/s11883-004-0101-yPubMedView ArticleGoogle Scholar
  31. Kusunoki M, Tsutsumi K, Sato D, Nakamura A, Habu S, Mori Y, Morishita M, Yonemoto T, Miyata T, Nakaya Y, Nakamura T: Activation of lipoprotein lipase increases serum high density lipoprotein 2 cholesterol and enlarges high density lipoprotein 2 particles in rats. Eur J Pharmacol 2011, 668: 337–339. 10.1016/j.ejphar.2011.06.040PubMedView ArticleGoogle Scholar
  32. Rashid S, Curtis DE, Garuti R, Anderson NN, Bashmakov Y, Ho YK, Hammer RE, Moon YA, Horton JD: Decreased plasma cholesterol and hypersensitivity to statins in mice lacking Pcsk9. Proc Natl Acad Sci U S A 2005, 102: 5374–5379. 10.1073/pnas.0501652102PubMed CentralPubMedView ArticleGoogle Scholar
  33. Graham MJ, Lemonidis KM, Whipple CP, Subramaniam A, Monia BP, Crooke ST, Crooke RM: Antisense inhibition of proprotein convertase subtilisin/kexin type 9 reduces serum LDL in hyperlipidemic mice. J Lipid Res 2007, 48: 763–767. 10.1194/jlr.C600025-JLR200PubMedView ArticleGoogle Scholar
  34. Chan JC, Piper DE, Cao Q, Liu D, King C, Wang W, Tang J, Liu Q, Higbee J, Xia Z, et al.: A proprotein convertase subtilisin/kexin type 9 neutralizing antibody reduces serum cholesterol in mice and nonhuman primates. Proc Natl Acad Sci U S A 2009, 106: 9820–9825. 10.1073/pnas.0903849106PubMed CentralPubMedView ArticleGoogle Scholar
  35. Fossati P, Romon-Rousseaux M: Insulin and HDL-cholesterol metabolism. Diabete Metab 1987, 13: 390–394.PubMedGoogle Scholar
  36. Bornfeldt KE, Tabas I: Insulin resistance, hyperglycemia, and atherosclerosis. Cell Metab 2011, 14: 575–585. 10.1016/j.cmet.2011.07.015PubMed CentralPubMedView ArticleGoogle Scholar
  37. Trauner M, Claudel T, Fickert P, Moustafa T, Wagner M: Bile acids as regulators of hepatic lipid and glucose metabolism. Dig Dis 2010, 28: 220–224. 10.1159/000282091PubMedView ArticleGoogle Scholar
  38. Urizar NL, Dowhan DH, Moore DD: The farnesoid X-activated receptor mediates bile acid activation of phospholipid transfer protein gene expression. J Biol Chem 2000, 275: 39313–39317. 10.1074/jbc.M007998200PubMedView ArticleGoogle Scholar
  39. Jiang XC, Bruce C, Mar J, Lin M, Ji Y, Francone OL, Tall AR: Targeted mutation of plasma phospholipid transfer protein gene markedly reduces high-density lipoprotein levels. J Clin Invest 1999, 103: 907–914. 10.1172/JCI5578PubMed CentralPubMedView ArticleGoogle Scholar
  40. Huuskonen J, Ekstrom M, Tahvanainen E, Vainio A, Metso J, Pussinen P, Ehnholm C, Olkkonen VM, Jauhiainen M: Quantification of human plasma phospholipid transfer protein (PLTP): relationship between PLTP mass and phospholipid transfer activity. Atherosclerosis 2000, 151: 451–461. 10.1016/S0021-9150(99)00429-3PubMedView ArticleGoogle Scholar
  41. Huuskonen J, Olkkonen VM, Ehnholm C, Metso J, Julkunen I, Jauhiainen M: Phospholipid transfer is a prerequisite for PLTP-mediated HDL conversion. Biochemistry 2000, 39: 16092–16098. 10.1021/bi0019287PubMedView ArticleGoogle Scholar
  42. Qiu G, Hill JS: Endothelial lipase promotes apolipoprotein AI-mediated cholesterol efflux in THP-1 macrophages. Arterioscler Thromb Vasc Biol 2009, 29: 84–91. 10.1161/ATVBAHA.108.176487PubMedView ArticleGoogle Scholar
  43. Borggreve SE, De Vries R, Dullaart RP: Alterations in high-density lipoprotein metabolism and reverse cholesterol transport in insulin resistance and type 2 diabetes mellitus: role of lipolytic enzymes, lecithin:cholesterol acyltransferase and lipid transfer proteins. Eur J Clin Invest 2003, 33: 1051–1069. 10.1111/j.1365-2362.2003.01263.xPubMedView ArticleGoogle Scholar
  44. Lamarche B, Rashid S, Lewis GF: HDL metabolism in hypertriglyceridemic states: an overview. Clin Chim Acta 1999, 286: 145–161. 10.1016/S0009-8981(99)00098-4PubMedView ArticleGoogle Scholar
  45. Frenais R, Ouguerram K, Maugeais C, Mahot P, Maugere P, Krempf M, Magot T: High density lipoprotein apolipoprotein AI kinetics in NIDDM: a stable isotope study. Diabetologia 1997, 40: 578–583. 10.1007/s001250050718PubMedView ArticleGoogle Scholar
  46. Hoang A, Murphy AJ, Coughlan MT, Thomas MC, Forbes JM, O’Brien R, Cooper ME, Chin-Dusting JP, Sviridov D: Advanced glycation of apolipoprotein a-I impairs its anti-atherogenic properties. Diabetologia 2007, 50: 1770–1779. 10.1007/s00125-007-0718-9PubMedView ArticleGoogle Scholar
  47. Stein EA, Gipe D, Bergeron J, Gaudet D, Weiss R, Dufour R, Wu R, Pordy R: Effect of a monoclonal antibody to PCSK9, REGN727/SAR236553, to reduce low-density lipoprotein cholesterol in patients with heterozygous familial hypercholesterolaemia on stable statin dose with or without ezetimibe therapy: a phase 2 randomised controlled trial. Lancet 2012, 380: 29–36. 10.1016/S0140-6736(12)60771-5PubMedView ArticleGoogle Scholar
  48. Stein EA, Swergold GD: Potential of proprotein convertase subtilisin/kexin type 9 based therapeutics. Curr Atheroscler Rep 2013, 15: 310.PubMedView ArticleGoogle Scholar
  49. Raal F, Scott R, Somaratne R, Bridges I, Li G, Wasserman SM, Stein EA: Low-density lipoprotein cholesterol-lowering effects of AMG 145, a monoclonal antibody to proprotein convertase subtilisin/kexin type 9 serine protease in patients with heterozygous familial hypercholesterolemia: the reduction of LDL-C with PCSK9 inhibition in Heterozygous Familial Hypercholesterolemia disorder (RUTHERFORD) randomized trial. Circulation 2012, 126: 2408–2417. 10.1161/CIRCULATIONAHA.112.144055PubMedView ArticleGoogle Scholar
  50. Frank-Kamenetsky M, Grefhorst A, Anderson NN, Racie TS, Bramlage B, Akinc A, Butler D, Charisse K, Dorkin R, Fan Y, et al.: Therapeutic RNAi targeting PCSK9 acutely lowers plasma cholesterol in rodents and LDL cholesterol in nonhuman primates. Proc Natl Acad Sci U S A 2008, 105: 11915–11920. 10.1073/pnas.0805434105PubMed CentralPubMedView ArticleGoogle Scholar
  51. Maxwell KN, Breslow JL: Adenoviral-mediated expression of Pcsk9 in mice results in a low-density lipoprotein receptor knockout phenotype. Proc Natl Acad Sci U S A 2004, 101: 7100–7105. 10.1073/pnas.0402133101PubMed CentralPubMedView ArticleGoogle Scholar

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