Perfluorooctanoate (PFOA) ; Plasma cholesterol ; Plasma triglycerides ; Lipoproteins ; Lipoprotein metabolism ; non-HDL-C/HDL-C ; APOE*3-Leiden.CETP mice
A recent article in Toxicology Reports by Rebholz et al.  reported increased plasma cholesterol levels (primarily as HDL) in C57BL/6 (male and female) and BALB/c (male only) mice given high fat (Westernized) diet which also contained PFOA. The authors concluded that PFOA ingestion leads to hypercholesterolemia and they stated these data were “consistent with human observational findings”. There are several key factors which have not been considered in their study and we offer this letter to identify this important information. In particular, we feel that this conclusion needs more balance, particularly with respect to the relevance and translatability of their findings to the human situation.
Conventional mouse strains used in preclinical biomedical and toxicological research, including the C57BL/6 mice and BALB/c mice studied by Rebholz et al., are considered not to be the most appropriate animal models to study modulation of lipoprotein metabolism, since lipolysis of TG-rich particles as chylomicrons and very low density lipoprotein (VLDL) and their remnants and clearance of the apoB-containing (non-HDL) lipoproteins via the apolipoproteinE-LDL-receptor (apoE-LDLR) pathway are fast processes as compared to humans  . Consequently, the mice have relatively low plasma TG and cholesterol levels with low levels of the atherogenic VLDL and LDL, and the majority of cholesterol is contained in HDL (Fig. 1 A,B). Severe dietary regimens with saturated fat and high amounts of cholesterol and cholic acid are required to increase the amount of non-HDL-C to some extent, but still lower than in humans  .
Mice have a fast clearance of apoB-containing lipoproteins and do not express CETP (A), as a result the majority of plasma cholesterol is confined to HDL (B), with TC and TG levels of 1.5–2.0 and 0.2–0.3 mmol/L in C57BL/6 mice. Humans have a slower clearance of apoB-containing lipoproteins and do express CETP (C) and normolipidemic man have TC and TG levels of <5.2 and 0.5–1.5 mmol/L, respectively, and cholesterol consists mainly of non-HDL-C (VLDL-C/LDL-C) (D). The APOE*3-Leiden.CETP mouse has a lipoprotein profile similar as in FD patients and a lipoprotein metabolism similar to that in man (E), and on a chow diet TC and TG levels are 3.0–4.0 and 2.5–3.0 mmol/L, mainly confined to the non-HDL-C fraction (F).
In contrast in humans, lipolysis is slower and removal of apoB-containing lipoproteins is delayed  . In addition, humans unlike mice possess an important player in lipoprotein metabolism, cholesterol ester transfer protein (CETP), which transfers cholesterol from HDL to (V)LDL in exchange for triglycerides, thereby increasing (V)LDL-C levels and decreasing HDL-C. Due to these differences, cholesterol is contained mainly in LDL and to a lesser extent in HDL (Fig. 1 C,D).
To develop a mouse model with a more human-like lipoprotein metabolism for pharmacological and toxicological research, the APOE*3-Leiden transgenic mouse was generated by the introduction of a genomic human DNA construct carrying the mutant APOE*3-Leiden gene, the APOCI gene, and all known regulatory elements, obtained from a patient with Familial Dysbetalipoproteinemia (FD)  . These mice were cross-bred with mice expressing human CETP under control of its natural flanking regulatory DNA-sequences  to obtain the APOE*3-Leiden.CETP mouse, as a humanized model for FD and mixed dyslipoproteinemia  . While normal wild-type mice have a very rapid clearance of apoB-containing lipoproteins, APOE*3-Leiden(.CETP) mice have an impaired clearance and increased TG level, and are thereby mimicking the slow clearance observed in humans, particularly in patients with FD  ,  and  . Importantly, as compared to the widely used hyperlipidemic and atherogenic apoE- and LDLR-deficient (E0/0 and LDLR0/0) mice, the APOE*3-Leiden(.CETP) mice possess an intact but delayed apoE-LDLR-mediated clearance, which is essential for the proper, human-like response on hypolipidemic drugs  . APOE*3-Leiden.CETP mice respond well to dietary intervention using human-relevant (Westernized) diets with increases in plasma cholesterol and TG and these lipids can be titrated to levels mimicking those in humans.
As background, FD or type III hyperlipoproteinemia is characterized by elevated levels of plasma cholesterol and an increased ratio of cholesterol to TG in the VLDL and intermediate-density lipoprotein (IDL) fractions, resulting in the appearance of β-VLDL particles ( ). Similarly as in FD patients, in APOE*3-Leiden and APOE*3-Leiden.CETP mice the major part of plasma cholesterol is contained in the VLDL and VLDL-remnant particles, leading to formation of β-VLDL particles, which is further increased by cholesterol feeding  and  (Fig. 1 E,F).
With respect to response to hypolidemic drugs and contrary to wildtype or E0/0 and LDLR0/0 mice and other species  , the APOE*3-Leiden(.CETP) mice respond in a similar way to statins as humans do, both with respect to direction and magnitude of the change with decreases in the apoB-containing lipoproteins up to 55% ( ,  and  ). In addition, the extent of lipid-lowering and change in lipoprotein profile observed with fibrates ( ,  and  ), niacin ( ,  and  ) and the new anti-PCSK9 therapy with monoclonal antibodies ( and  ) in APOE*3Leiden(.CETP) mice is comparable to that of hyperlipidemic and FD patients.
To explore the effects of PFOA on lipoprotein metabolism in this mouse model, we recently started to investigate the effects of environmentally and occupationally relevant PFOA exposure in male APOE*3-Leiden.CETP mice fed a Western-type diet. Our preliminary data showed that dietary intake of PFOA reduced plasma TG and cholesterol levels with the cholesterol reduction confined to the apoB-containing (non-HDL-C) lipoproteins.
In support of the translatability of the APOE*3-Leiden.CETP mouse for investigation of the mechanistic background of alterations in lipid and lipoprotein metabolism, the reduction in non-HDL-C found in our study as well as data reported by Loveless et al.  is consistent with results from a phase I trial with PFOA in humans. In that study, 41 cancer patients were given ammonium PFOA doses of up to 1200 mg/week for a median of 6.5 weeks, which resulted in a reduction of non-HDL-C as a treatment effect  .
The increase of plasma cholesterol reported by Rebholz et al., was confined to HDL-C, whereas we and others found a decrease in (V)LDL-C (non-HDL-C) after PFOA exposure. The question then arises how these alterations in lipoprotein metabolism translate into cardiovascular risk. LDL-C is recognized as a primary causal risk factor in cardiovascular disease as evidenced from many experimental, epidemiological and genetic studies  . In addition, intervention trials with statin therapy confirm a reduced incidence of coronary heart disease as a consequence of cholesterol-lowering in LDL  and  and recent trials indicate that intensive lipid-lowering with statins may be more beneficial in risk reduction than less intensive (or standard) therapy  . According to results from the latter meta-analysis, every 1 mmol/L (40 mg/dL) reduction in LDL-C is associated with a 22% reduction in the risk of major vascular events suggesting that a 2–3 mmol/L reduction in LDL-C would correspond with a 40–50% reduction in events.
Epidemiological studies consistently report an inverse association between coronary heart disease risk and HDL-C: Results from 4 prospective epidemiologic studies indicate that an increase of 1 mg/dL (0.03 mM) in HDL-C is associated with a 2–3% reduction in risk  .
Besides its major role in reverse cholesterol transport, HDL has also been described to have anti-inflammatory, anti-oxidant, anti-platelet and vasodilatory properties and may therefore have a protective role in coronary heart disease  . Several therapeutic approaches aimed at raising HDL-C levels have since been investigated. However, undisputed proof for causality of low HDL-C in cardiovascular disease is lacking and clinical trials aimed at raising HDL-C to prevent disease (AIM-HIGH, HPS2-THRIVE, dal-OUTCOMES) have failed to meet their primary goals  . In addition, data from Mendelian randomization studies show that HDL-C and myocardial infarction risk are not causally related  .
For a systematic review and meta-analysis of relevant preclinical studies and clinical trials on the contribution of non-HDL-C/LDL-C-lowering versus HDL-C-raising we refer to Kühnast et al.  . In this review we investigated the effects of established and novel treatment strategies, specifically targeting HDL, on inhibition of atherosclerosis development in CETP-expressing animals, since CETP is a crucial gene involved in HDL-C metabolism and implicated in the mechanisms by which most therapies modulate HDL-C  . In addition, we conducted a meta-analysis to evaluate the potential effects of these treatment strategies on the prevention of clinical events in randomized controlled trials, focusing specifically on the contribution of non-HDL-C/LDL-C-lowering versus HDL-C-raising. We conclude that the protective role of lowering LDL-C and non-HDL-C is well-established. The contribution of raising HDL-C on inhibition of atherosclerosis and the prevention of cardiovascular disease remains undefined and may be dependent on the mode of action of HDL-C-modification. Similar outcome data were found for the prevention of clinical events in randomized controlled trials and on inhibition of atherosclerosis in relevant, CETP-expressing, animals emphasizing the validity/translatability of these animal models to the human situation  .
Rebholz et al. conclude “To summarize, we have shown that C57BL/6 and male BALB/c mice exposed to PFOA have significantly increased plasma cholesterol levels when fed Westernized diets, consistent with human observational findings at the national [refs 39,14 therein] and community levels [refs 16,19,60 therein] and in adolescent [refs 18,20 therein] and occupational [refs 44,56,57,9 therein] cohorts”. As discussed above, there are a number of issues with the outcome of their study and extrapolation of the data from a study in wildtype mice to the human situation. The choice of the mouse model should be carefully considered, given its inherent differences in lipoprotein metabolism and distribution of cholesterol among lipoproteins between wildtype mice and man, as well as the differences in changes in lipoproteins induced by PFOA and the potential cardiovascular risk raised by these changes. For all the reasons articulated above we felt it is premature for Rebholz et al. to conclude that PFOA causes hypercholesterolemia in these mice fed Westernized diets.
This work was funded in part by an unrestricted educational grant from 3M Corporation to TNO-Metabolic Health Research but represents an independent opinion of the authors.
Hans M.G. Princen and Elsbet J. Pieterman report grants from 3M Company during the conduct of the study and outside the submitted work. Marianne G. Pouwer has nothing to disclose.
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