DHA and EPA reverse cystic fibrosis-related FA abnormalities by suppressing FA desaturase expression and activity.

Patients and models of cystic fibrosis (CF) exhibit consistent abnormalities of polyunsaturated fatty acid composition, including decreased linoleate (LA) and docosahexaenoate (DHA) and variably increased arachidonate (AA), related in part to increased expression and activity of fatty acid desaturases. These abnormalities and the consequent CF-related pathologic manifestations can be reversed in CF mouse models by dietary supplementation with DHA. However, the mechanism is unknown. This study investigates this mechanism by measuring the effect of exogenous DHA and eicosapentaenoate (EPA) supplementation on fatty acid composition and metabolism, as well as on metabolic enzyme expression, in a cell culture model of CF. We found that both DHA and EPA suppress the expression and activity of Δ5- and Δ6-desaturases, leading to decreased flux through the n-3 and n-6 PUFA metabolic pathways and decreased production of AA. The findings also uncover other metabolic abnormalities, including increased fatty acid uptake and markedly increased retroconversion of DHA to EPA, in CF cells. These results indicate that the fatty acid abnormalities of CF are related to intrinsic alterations of PUFA metabolism and that they may be reversed by supplementation with DHA and EPA.

Western University, Cleveland, OH). The cells were grown in culture fl asks precoated with LHC Basal media (Invitrogen, Carlsbad, CA) containing a mixture of 3 g/ml vitrogen (Angiotech Biomaterials, Palo Alto, CA), 10 g/ml human fi bronectin (Sigma-Aldrich, St. Louis, MO), and 0.1 mg/ml BSA (BSA; Sigma-Aldrich). The cells were maintained at 37°C in 5% CO 2 in MEM + glutamax (Invitrogen), supplemented with 10% horse serum (Omega Scientifi c, Tarzana, CA), penicillin (100 U/ml), and streptomycin (100 g/ml). Horse serum was used because of its higher concentration of LA, which allows fatty acid changes in CF cells to be manifested ( 11 ). The medium was changed three times per week.

Fatty acid supplementation
For each experiment, WT and CF cells were seeded onto 6-well plates at 3 × 10 5 and 1 × 10 5 cells/well respectively. The cells were allowed to grow until 1 day postconfl uence (typically 6 days), the point at which fatty acid changes are maximized ( 11 ), after which they were supplemented with 0, 5, 10, or 20 M fatty acid for 24 h without prior serum deprivation. The supplementation medium was made by using free fatty acid dissolved in chloroform-methanol (2:1). The fatty acids were dried under nitrogen, and medium containing 10% reduced-lipid FBS or horse serum was added to the tube and sonicated three times for 5 s each, allowing binding by serum albumin.

Fatty acid composition analysis
After 24 h incubation with or without fatty acid supplementation, cells were washed twice in ice-cold PBS, scraped, and transferred to a glass tube, and 10 g heptadecanoate was added as an internal standard. Lipids extraction was performed using a modifi cation of the method of Folch et al. ( 33 ). Specifi cally, the cells were pelleted by centrifugation (100 g , 8 minutes) and dissolved in 6 vol of chloroform-methanol (2:1 v/v). They were then incubated on ice for 10 min, vortexed, and centrifuged (1,100 g , 10 minutes). The lower organic phase was transferred to a new glass tube and dried completely under nitrogen. Fatty acids were methylated using boron trifl uoride (BF 3 ; 14% in methanol; Sigma Aldrich) and a methanolic-base reagent ( 34 ) by adding 0.5 ml 0.5 N methanolic NaOH (Acros Organics, Geel, Belgium) to the sample, vortexing, and heating at 100°C for 3 min, followed by addition of 0.5 ml BF 3 at 100°C for 1 min. FAMEs were extracted by sequential addition of 1 ml hexane and 6.5 ml saturated NaCl solution. The sample was then vortexed and centrifuged (500 g , 4 minutes). The upper hexane layer was used for quantifi cation of FAMEs by gas chromatography (GC) using an Agilent 7980A GC system (Agilent Technologies, Santa Clara, CA) equipped with a Supelcowax SP-10 capillary column (Supelco, Bellefonte, PA) coupled to a mass spectrometer (model 5975C, Agilent Technologies). FAME mass was determined by comparing areas of unknown FAMEs to that of the internal standard. Results were expressed as the molar percentage (mol%) of each FAME relative to the total FAME mass of the sample, as previously described ( 10 ).

Fatty acid labeling experiments
After a 24 h incubation with or without fatty acid supplementation, the cells were incubated with medium containing 4.1 M [1-14 C]LA, LNA, AA, or EPA for 4 h and then harvested. Lipids were extracted and methylated as above, except that the fi nal hexane layer was dried under nitrogen and reconstituted in 50 l acetonitrile for HPLC analysis. Samples were separated by reverse-phase HPLC using a 4.6 × 250 mm, 5 m Agilent Zorbax Eclipse XDB-C18 column on an Agilent 1200 series instrument. A guard column (4.6 × 12.5 mm, 5 m) was paired with the analytical enzymes are associated with increases in palmitoleate, oleate, and Mead acid ( 24 ). CF cells have lower levels of DHA and DPA with decreased metabolism from their precursors, EPA and AA, respectively. We originally hypothesized that this was due to metabolic shunting of EPA and AA away from DHA and DPA toward eicosanoid production.
An important advance in understanding the role of these metabolic abnormalities in the pathogenesis of CF has come from mouse models. Studies in two different mouse models of CF ( 6,8 ) demonstrated normalization of LA and AA levels in lung, intestine, and pancreas after dietary supplementation with DHA. Furthermore, this treatment corrected the phenotypic manifestations of CF, decreasing ileal villus height, pancreatic duct diameter, and pulmonary infl ammation stimulated by lipopolysaccharide ( 6,25 ). Similarly, CF patients treated with DHA exhibited signifi cant decreases in plasma AA levels (26)(27)(28), accompanied in some cases by increased LA ( 29,30 ). Despite moving the fatty acid alterations in CF toward normal, the clinical outcomes in these small studies have been inconsistent. DHA supplementation of CF patients, often for short periods of time at low doses, reduced markers of infl ammation but did not convincingly improve symptoms in most studies (reviewed in Refs. [3][4][5]. The mechanism by which DHA corrects these n-6 fatty acid abnormalities in CF is unknown. As detailed above, recent studies show that these abnormalities are associated with increased expression and activity of ⌬ 5-and ⌬ 6desaturase ( 23 ), but they do not establish a causal relationship. This requires demonstrating that the fatty acid abnormalities can be corrected by reversing the observed changes in enzyme activity. As these enzymes are regulated primarily at the transcriptional level ( 31 ) and as DHA plays a signifi cant role in this regulation in metabolic tissues, such as liver ( 32 ), we hypothesized that suppression of AA production by DHA in CF is due to downregulation of these enzymes. The current study tests this hypothesis by examining the effects of DHA and the related n-3 fatty acid EPA on the composition and metabolism of PUFAs in CF cells and on the expression and activity of fatty acid desaturases. The results establish a mechanistic link between enzyme expression and fatty acid composition alterations in CF.
As expected, DHA treatment increased DHA levels in both types of cells, although the increase was much higher in CF cells (6.9 mol%) than in WT cells (4.6 mol%), such that DHA levels were signifi cantly higher in DHA-treated CF cells compared with their WT cell counterparts. DHA treatment also caused a signifi cant change in AA levels in CF cells, which were reduced to WT cell levels. To determine whether this change was due to decreased metabolism of LA to AA, CF and WT cells were incubated with increasing concentrations of DHA for 24 h, followed by [ 14 C]LA for 4 h. Fatty acids were extracted, and conversion of radiolabeled LA to AA was measured as described in Materials and Methods . The results showed a dose-dependent decrease in production of labeled AA corresponding to increased LA ( Fig. 2A ), indicating suppression of LA to AA metabolism by DHA. This decrease was observed in both CF and WT cells, although CF cells appeared to be more sensitive to DHA treatment, with greater suppression of labeled AA production, particularly at 5 M and 10 M concentrations, shifting the curve to the left.
Unlike AA, EPA levels in CF cells were signifi cantly increased by DHA treatment, with no change in WT cells ( Fig. 1 ). It is unlikely that this is due to increased production of EPA from LNA, as LNA levels are so low. Furthermore, labeling experiments with [ 14 C]LNA ( Fig. 2B ) indicated that conversion of LNA to EPA, which was markedly higher in CF cells at baseline, was reduced to almost WT levels by increasing concentrations of DHA. A second possibility is that increased EPA levels are due to retroconversion of DHA to EPA, as has been previously described ( 36,37 ). In fact, calculated retroconversion [ ⌬ EPA/ ( ⌬ EPA+ ⌬ DHA)] ( 38 ) is much higher in CF cells (20%) than in WT cells (1%).
To determine the specifi city of these effects, cells were incubated with saturated and monounsaturated fatty acids. Incubation of WT and CF cells with 20 M palmitate (PA; 16:0) ( Fig. 2C ) or oleate (OA; 18:1n-9) (data not shown) had no effect on the metabolism of LA to AA.
DHA treatment further decreased metabolism of AA in the n-6 pathway. Levels of the AA metabolite 22:4n-6 were signifi cantly reduced in both WT and CF cells ( Fig. 1 ), whereas DPA levels were decreased in WT cells only. DPA levels in CF cells, already very low, were decreased but not by a statistically signifi cant margin. Labeling studies with [ 14 C]AA confi rmed a marked decrease in AA to DPA metabolism ( Fig. 3A ) in WT cells. This conversion was markedly reduced at baseline in CF cells and showed a modest decline with DHA supplementation.
The effect of DHA on EPA metabolism was complex. Levels of the immediate elongation product of EPA, 22:5n-3, were reduced in CF cells with DHA treatment, despite the signifi cant increase in EPA levels ( Fig. 1 ). column. For separation, a gradient system consisting of solvent A (HPLC grade H 2 0 + 0.02% H 2 PO 4 ) and solvent B (100% HPLC grade acetonitrile) was used, with a fl ow rate of 1 ml/min. For n-3 fatty acids, the following program was used: 76% B for 0.5 min, 76-86% B for 10 min, hold for 20 min, 86-100% B for 2 min, hold for 18 min, and then reconstitution of the starting conditions. For n-6 fatty acids, the program was 58% B for 25 min, 58-61% B for 2 min, hold for 8 min, 61-100% B for 15 min, hold for 20 min, and then reconstitution of the original conditions. Peaks were identifi ed by UV detection at 205 nm, and their identity was determined by comparing peak retention time with that of unlabeled FAME standards. Radiolabeled peaks were quantifi ed using a ␤ -RAM scintillation detector (counting effi ciency >90% for 14 C with 5 CPM background) coupled to the HPLC instrument. Results are expressed as percentage of total measured counts in the sample.

Quantitative real-time PCR
Total RNA was isolated from sense and antisense cells using TRIzol reagent (Invitrogen) according to the manufacturer's instructions. RNA samples were treated with DNase I (DNA-free kit; Ambion, Inc., Austin, TX), and fi rst strand cDNA was synthesized from 2 g total RNA with random hexamer primers, using Taq-Man Reverse Transcription Reagents (Applied Biosystems, Foster City, CA). The qPCR reaction was carried out in a total volume of 20 l, using 10 l 2× Power SYBR Green PCR Master Mix (Applied Biosystems), 50 ng of reverse-transcribed total RNA, and 156 nM forward and reverse primers. Primer design and sequences were as previously described ( 23 ). All reactions were performed in triplicate in 96-well plates on a CFX96 system (Bio-Rad), and the data were analyzed using CFX Manager software (Bio-Rad). The relative amount of mRNA was calculated using the comparative C T method, with RPLP0 mRNA serving as an invariant control.

Statistical analysis
Quantitative data for multiple groups (WT and CF cells, with or without fatty acid supplementation) were compared using twoway ANOVA with Bonferroni posttest for pair-wise comparisons using Prism 5 (GraphPad Software, La Jolla, CA).

RESULTS
Experiments were performed in a cell culture model of CF, 16HBE human bronchial epithelial cells stably transfected with a plasmid expressing the fi rst 131 nucleotides of the CFTR gene in either the sense (WT cells) or antisense (CF cells) orientation ( 35 ). Compared with WT cells, CF cells exhibit signifi cant loss of both CFTR expression and function ( 35 ), and they exhibit fatty acid abnormalities similar to those of CF patients ( 11 ).
To ascertain the effect of DHA treatment on total fatty acid profi les, WT and CF cells were incubated in the presence or absence of 20 M DHA for 24 h prior to measurement of relative fatty acid concentrations ( Fig. 1 ). In the absence of DHA, the fatty acid profi les were similar to those in prior studies ( 10,11,23 ). In particular, LA levels were decreased in CF cells, with increased levels of 18:3n-6, 20:3n-6, AA, and EPA, indicative of increased metabolism of LA to AA and of LNA to EPA. The fatty acid profi les were also indicative of decreased metabolism of AA and EPA to downstream products in CF cells. Both 22:4n-6 and DPA were signifi cantly reduced in CF cells, as was DHA. higher in WT than CF cells for both 22:5n-3 (78% versus 27%) and DHA (42% versus 11%). Consequently, DHA levels remained signifi cantly lower in CF than WT cells. These fi ndings correlate with much lower conversion of labeled EPA to DHA in CF cells at all concentrations of EPA ( Fig. 6B )

. For both CF and WT cells, this conversion
This diminution is confi rmed by labeling studies that show a 60% decrease in conversion of [ 14 C]EPA to DHA in CF cells ( Fig. 3B ). Levels of 22:5n-3 were essentially unchanged in DHA-treated WT cells ( Fig. 1 ). Labeled DHA production from EPA actually increased at lower DHA concentrations (5 M and 10 M) and then showed a minimal decline from baseline at 20 M DHA ( Fig. 3B ).
To determine whether the effect of DHA was specifi c, WT and CF cells were also incubated with EPA, and the effects on fatty acid composition and metabolism were measured. Fig. 4 shows the fatty acid composition of WT and CF cells with and without 24 h incubation with 20 M EPA. Similar to what was observed for DHA treatment, CF cells demonstrated a greater increase in EPA (5.0 mol%) than WT cells (0.9 mol%), further increasing the EPA disparity between the cells.
The effects of EPA on fatty acid metabolism were also similar to those of DHA. EPA treatment led to decreased levels of both 20:3n-6 and AA in WT and CF cells, corresponding to a dose-dependent decrease in labeled LA incorporation into AA ( Fig. 5A ). There was a similar decrease in conversion of LNA to EPA ( Fig. 5B ), although the effects of this change on EPA levels ( Fig. 4 ) are obscured by incorporation of exogenous EPA. In both cases, the effect of EPA appeared to be greater in CF than in WT cells. These data indicate that EPA suppresses metabolism of LA and LNA, similar to DHA.
EPA also reduced further metabolism of AA in the n-6 pathway. Levels of the AA metabolites 22:4n-6 and DPA were reduced in EPA-treated WT and CF cells ( Fig. 4 ) in a pattern almost identical to that of DHA treatment ( Fig. 1 ). Labeling studies with [ 14 C]AA confi rmed a marked decrease in AA to DPA metabolism ( Fig. 6A ) in WT cells. This conversion was markedly reduced at baseline in CF cells and showed a modest decline at 20 M EPA.
As expected, increased EPA after treatment led to increases in the EPA metabolites 22:5n-3 and DHA ( Fig. 4 ). However, the increases were more signifi cant in WT than CF cells. Conversion rates [calculated as ⌬ product / ( ⌬ substrate + ⌬ product ), where ⌬ represents the fatty acid level after DHA treatment subtracted from the baseline level] were much  qRT-PCR in WT and CF cells after incubation with varying concentrations of DHA and EPA ( Fig. 7 ). At baseline, mRNA levels of ⌬ 5-and ⌬ 6-desaturases were signifi cantly higher (approximately 2-fold) in CF than WT cells ( P < 0.05 for each comparison). Incubation with as little as 5 M DHA or EPA reduced expression of these genes in CF cells to the level of WT cells ( Fig. 7A, B ). Expression of elongases 2 and 5 was either slightly decreased or unchanged ( Fig. 7C, D ). These data suggest that the reduction of fatty acid metabolism observed with both DHA and EPA incubation is due to downregulation of desaturase gene expression.
To determine the specifi city of these effects, WT and CF cells were incubated with LNA, AA, PA, and OA, all at 20 M. Both LNA and AA reduced the expression of desaturases, but to a lesser degree compared with DHA and EPA (not shown). For example, LNA and AA reduced ⌬ 6-desaturase mRNA by 48% and 45%, respectively, whereas DHA and EPA reduced expression by 68% and 73%, respectively, at 20 M. Similar results were seen for ⌬ 5-desaturase. There was little or no signifi cant effect on gene expression after incubation with PA ( Fig. 7E ) or OA (not shown).

DISCUSSION
While alterations in PUFA levels in CF are a well-established phenomenon, a precise mechanism to explain these changes has not been defi nitively established. A number of hypotheses have been advanced, including increased AA release and eicosanoid metabolism ( 4 ), changes in thiol and phospholipid metabolism ( 5 ), and increased fl ux within PUFA metabolic pathways ( 10 ). Work from our laboratory provided correlative data suggesting that these metabolic changes were due to increased expression and activity of fatty acid desaturases ( 23,24 ). The current study demonstrates that treatment of CF cells with exogenous DHA reverses the metabolic changes by suppressing expression of these enzymes. Specifi cally, DHA decreases expression of ⌬ 5-and ⌬ 6-desaturases, leading to decreased conversion of LA to AA in the n-6 metabolic pathway, thereby reversing the PUFA abnormalities. This study was increased at lower concentrations of EPA (5 M and 10 M) and then returned to roughly baseline levels at 20 M ( Fig. 6B ), similar to the effect of DHA supplementation ( Fig. 3B ).
Previous studies ( 23 ) have shown that the differences in LA and LNA metabolism in CF cells are associated with increased expression of ⌬ 5-and ⌬ 6-desaturase enzymes, which are primarily regulated at the transcriptional level ( 31 ). Therefore, we hypothesized that the effects of DHA and EPA on metabolism may be due to changes in the expression of these enzymes. To test this, we measured the expression of the four major enzymes in the n-3 and n-6 metabolic pathways ( ⌬ 5-and ⌬ 6-desaturases, plus elongases 2 and 5) by  that DHA therapy reduces AA levels in CF patients and animal models ( 6,(25)(26)(27)(28)(29)(30).
To test the specifi city of the DHA effect, all of the experiments were repeated using the related n-3 fatty acid EPA. Interestingly, there was little difference in the effects of EPA versus DHA on PUFA metabolism. Both caused downregulation of desaturase gene expression and reduced metabolism of LA and LNA to AA and EPA, respectively. Both had similar effects on fatty acid composition. LNA, the precursor of all n-3 fatty acids, and AA, an n-6 fatty acid, had similar, although smaller effects. Saturated (PA) and monounsaturated (OA) fatty acids had no effect. These in vitro fi ndings contrast with those in a mouse model ( 6 ), which showed a benefi cial effect of DHA treatment on CF pathology, but no effect with EPA or LNA treatment. The reason for this difference is unclear. Human trials ( 39 ) have shown differences in metabolism using EPA alone or combinations of EPA and DHA ( 29,30,40,41 ). However, the individual effects of EPA and DHA are diffi cult to disaggregate, as supplementation with either of these fatty acids increases concentrations of the other. It is also possible that species differences may play a role.
Unlike previous studies that have focused exclusively on n-6 PUFA metabolism, the current work also examines the n-3 pathway. As indicated above, these are parallel pathways in which the metabolic reactions are catalyzed by a common set of enzymes. Although the metabolic alterations at baseline and with PUFA treatment are similar in direction, there are striking changes in degree that appear to be accentuated in CF. For example, the n-3 pathway appears to be more active than the n-6 pathway, particularly in CF cells, as was reported previously ( 23 ) and confi rmed in the current study ( Figs. 1 and 2 ). This may refl ect a preference of the common desaturase and elongase enzymes for substrates of the n-3 pathway, as has been described by others ( 42,43 ). This difference is apparent in the response to DHA and EPA, as these fatty acids induce a greater decline in LA to AA than in LNA to EPA metabolism and a greater effect in CF than WT cells ( Figs. 2 and 5 ). However, the disparity in EPA levels observed between WT and CF cells has not been consistently described in patients. The most likely explanation for this is that dietary n-3 fatty acids, particularly LNA, are relatively underrepresented in the Western diet ( 44 ).
The current DHA supplementation data identify another source of EPA, that generated by retroconversion from DHA. This is a previously described phenomenon wherein DHA is shortened and desaturated by modifi ed ␤ -oxidation in peroxisomes ( 36,37 ). Interestingly, this process appears to be markedly upregulated in CF cells compared with WT cells. This fi nding suggests that retroconversion may be a second mechanism of increased EPA and decreased DHA levels in these cells. It also raises the possibility that DHA retroconversion is a regulated process, as has been suggested by others ( 45 ). This may have implications for the n-3 dietary treatment regimens for many diseases, including CF. Furthermore, CF may be a particularly good system for the study of this poorly understood metabolic pathway.
demonstrates that altered desaturase activity plays a role in abnormal fatty acid metabolism in CF. Furthermore, it provides a mechanistic explanation for the observation  pathway was actually increased. One possible explanation is that the increased concentrations of these fatty acids stimulate activity in their own metabolic pathway, perhaps by mass action, which effectively cancels their effects on enzyme expression.
A fi nal metabolic abnormality highlighted by the current data is a disparity in fatty acid uptake between WT and CF cells. For both DHA and EPA, CF cells appeared to incorporate more exogenous fatty acid than WT cells (compare DHA and EPA levels in Figs. 1 and 4 , respectively), consistent with previous fi ndings ( 10 ). The causes of this observation are unknown, but it may indicate increased fatty acid transport into CF cells. Recent studies have highlighted the importance of fatty acid transport and its regulation in metabolic diseases (reviewed in Ref. 47 ). It is possible that the differential effects of DHA and EPA on desaturase gene expression in CF and WT cells may be due to increased uptake of these fatty acids. Future investigation of the mechanism of this disparity in CF may contribute to the understanding of this process.
The complete link between CFTR mutations and the observed PUFA abnormalities in CF remains unknown. However, the identifi cation in this study of a proximal mechanism, upregulation of desaturase expression, is a step toward this ultimate goal. A number of transcription factors are known to participate in the PUFA-mediated regulation of ⌬ 5-and ⌬ 6-desaturase expression ( 31,48 ). Two of the most prominent, sterol regulatory element-binding protein (SREBP )-1 and peroxisome proliferator-activated receptor (PPAR) ␣ , exhibit altered expression and/or activity in CF (49)(50)(51). Identifi cation of the relevant transcription factor may identify signaling pathways connecting fatty acid metabolism to CFTR .
An important caveat to this study is that it is restricted to bronchial epithelial cells in culture. In contrast, Mailhot et al. ( 52 ) showed no apparent increase in LA to AA metabolism in CFTR-negative intestinal epithelial cells. In addition, Bhura-Bandali et al. ( 53 ) demonstrated decreased incorporation of exogenous LA into pancreatic duct cells carrying the ⌬ F508 mutation. While there are signifi cant methodologic differences between these results and the current study, making direct comparison diffi cult, it is also possible that the observed alterations are cell-type specifi c. Future studies using animal models will attempt to reconcile these differences by assessing PUFA metabolism across tissue types.
This study highlights the possible connection between AA and the phenotypic manifestations of CF. AA is a precursor of bioactive oxygenated metabolites known as eicosanoids, which include prostaglandins and leukotrienes. Production of these metabolites is known to be increased in CF, and several studies have drawn a connection between eicosanoid alterations and disease pathogenesis (54)(55)(56)(57)(58)(59). It is plausible that the observed benefi t of n-3 fatty acid therapy in the CF mouse model ( 6 ) and in a small subset of human trials ( 29,30 ) is due to its ability to normalize AA levels and, consequently, reduce excessive production of eicosanoids. In fact, changes in leukotriene metabolism have been noted in In addition to their effects on LA and LNA metabolism, DHA and EPA reduce metabolism of AA to DPA, particularly in WT cells. This may also be due to decreased ⌬ 6desaturase, which is involved in this pathway. It may also be due to suppression of fatty acid elongases, which are also regulated by these fatty acids ( 46 ). Interestingly, DHA and EPA did not signifi cantly reduce conversion of EPA to DHA. In fact, at lower concentrations, the activity of this Fig. 7. Changes in ⌬ 5-and ⌬ 6-desaturase mRNA expression with DHA and EPA supplementation. WT and CF cells were cultured in complete medium for 6 days, after which medium was replaced with either unsupplemented medium or medium containing 5, 10, or 20 M DHA (A-D, left) or EPA (A-D, right). After 24 h, the cells were harvested, and total RNA isolated as described in Materials and Methods . qRT-PCR was performed using primers for the mRNA sequences of ⌬ 5-desaturase ( FADS1 ) (A), ⌬ 6-desaturase ( FADS2 ) (B), elongase 2 ( ELOVL2 ) (C), or elongase 5 ( ELOVL5 ) (D). As a control, ⌬ 5-and ⌬ 6-desaturase mRNA levels were measured after exposure to 20 M PA for 24 h (E). Relative expression was determined by the ⌬ ⌬ C T method using ribosomal protein RPLP0 as a control. Data points represent mean ± SEM (n = 3). The fi ndings are representative of at least three independent experiments. several of these trials (39)(40)(41). More extensive studies in animal models and CF patients are required to confi rm these early observations. CF remains a deadly disease in need of new therapeutic approaches based on a better understanding of pathophysiology. The current study contributes to a mechanistic explanation for the very consistent PUFA metabolic abnormalities observed in CF and provides a basis for understanding how dietary lipid therapy might be able to modulate these changes. These fi ndings provide an enhanced framework for future studies of the role of lipid metabolism in the pathophysiology and therapy of this disease.