Prostasin, a membrane-bound serine protease, is known to increase the activity of the epithelial sodium channel (ENaC). Gene expression of prostasin was shown to be regulated by aldosterone, which increases the rate of sodium reabsorption through ENaC. To clarify the physiological relationships among prostasin, aldosterone and ENaC, we developed a specific radioimmunoassay (RIA) for human prostasin. Prostasin levels in urine were determined in 26 normotensive and 121 hypertensive subjects. Aldosterone content in urine and plasma, urinary Na/K ratio and other clinical parameters were also measured. We observed a highly significant correlation between prostasin and aldosterone concentration in urine (correlation coefficient: 0.673, P<0.0001). A significant correlation was also found between urinary prostasin and plasma aldosterone concentration (correlation coefficient: 0.229, P<0.05). In addition, urinary prostasin excretion was inversely correlated with urinary Na/K ratio (correlation coefficient: −0.425, P<0.0001). In conclusion, we developed a prostasin-specific RIA and applied it to the clinical study. Our findings suggest that urinary prostasin level is strongly correlated with urinary or plasma aldosterone level and may serve as a surrogate marker for ENaC activation in hypertensive patients. However, it is not clear, at the present time, whether endogenous aldosterone regulates prostasin expression or vice versa.
Aldosterone, a principal human mineralocorticoid hormone, is well known as the primary hormone that regulates salt balance, extracellular fluid volume and blood pressure (BP).1, 2, 3 It has also been reported that aldosterone enhances the rate of sodium reabsorption across epithelial cells of the distal nephron by increasing sodium transport through the epithelial sodium channel (ENaC), a principal physiological target of aldosterone,4, 5 consisting of three homologous subunits (α, β and γ).6, 7
In 1997, Vallet et al.8 identified a novel mechanism for the local regulation of ENaC activity. They cloned a trypsin family serine protease, xCAP1 (channel-activating protease 1), from a Xenopus kidney epithelial cell line (A6), by using a functional complementation assay designed to detect activators of ENaC in the Xenopus oocyte expression system. In this assay, they showed a two- to threefold activation of ENaC when xCAP1 was coexpressed with rat or Xenopus ENaC in oocytes. This effect is thought to rely on extracellular xCAP1 protease activity, as exposure of the apical membrane to the protease inhibitor aprotinin reduced amiloride-sensitive sodium transport. The first mammalian homologue of xCAP1, mouse CAP1 (mCAP1), was isolated from a mouse cortical collecting duct cell line.9 Vuagniaux et al.9 suggested that CAP1 is an orthologous gene for prostasin, and also showed that mCAP1 increases amiloride-sensitive sodium currents when coexpressed with ENaC in Xenopus oocytes.
Prostasin, a serine protease originally purified from human seminal fluid,10, 11, 12 is synthesized with a glycosylphosphatidylinositol membrane anchor and can also be secreted into physiological fluids.13 This protein is abundantly present in the seminal fluid, urine and prostate gland, and it is also present at moderate levels in the kidney, bladder, lung, colon, pancreas, salivary gland, bronchi, liver and endometrium.10, 11, 14, 15, 16 Prostasin has been identified as a potential regulator of amiloride-sensitive ENaC function in the kidney, lung and airways.17, 18, 19, 20, 21, 22, 23 However, the physiological role of this protein remains largely undetermined, although dysregulation of prostasin expression has been found in high-grade human prostate and breast cancers.14, 24, 25, 26 Catalytically active prostasin was detected in urine from both men and women.10 Although the concentration of prostasin in urine is lower than that in seminal fluid, the production of prostasin has to be very active in the kidney, considering the relatively large amount of the urine excreted in a day. These facts suggest the possibility that prostasin may play a key role in the regulation of renal tubular sodium transport by an autocrine and/or paracrine mechanism.
Recently, we also showed that rat CAP1/prostasin activates ENaC when the two are coexpressed in Xenopus oocytes, and that aldosterone substantially increases prostasin expression with functional consequences on sodium balance in vivo.27 Furthermore, we showed that urinary excretion of prostasin in patients with primary aldosteronism was substantially elevated and normalized after adrenalectomy.19 Regarding urinary prostasin, Olivieri et al.20 showed that spironolactone increased the urinary Na/K ratio and decreased urinary prostasin level in normotensives in whom the renin–aldosterone axis was activated by a low sodium intake, suggesting the regulation of urinary prostasin by aldosterone. On the contrary, however, one report presented evidence that the expression of prostasin by adenovirus-mediated human prostasin gene delivery resulted in a subsequent increase in aldosterone production and hypertension in rats.28 BP increase was accompanied by elevated plasma aldosterone after prostasin gene transfer, before the development of hypertension, indicating that stimulation of aldosterone production is the primary target of prostasin. Accordingly, it is unclear whether aldosterone increases prostasin expression or, on the contrary, if preceding stimulation of prostasin leads to the release of aldosterone from adrenal gland. To determine the role of prostasin in the pathophysiology of hypertension or hyperaldosteronism, it is important to develop a prostasin-specific and high-sensitive assay method. Therefore, in this article, we describe the development of a specific radioimmunoassay (RIA) for human prostasin and its application to the evaluation of prostasin levels in urine from normotensive and hypertensive subjects. The physiological relationships among prostasin, BP, aldosterone and ENaC function were analyzed and discussed.
Purification of recombinant human prostasin
A cDNA for recombinant human prostasin was created by inserting an enterokinase cleavage site, Asp-Asp-Asp-Asp-Lys, between the light chain and heavy chain and by replacing the C-terminal membrane anchoring domain with a 6 × His tag, so that the recombinant protein could be secreted as a proprotein and could be activated by exogenous enterokinase treatment. The cDNA was subcloned into the transfer vector pM00001 (Katakura Industries, Saitama, Japan). Linearized hybrid baculovirus DNA ‘Bac-Duo’ (Katakura Industries) was co-transfected with the recombinant plasmid into a Spodoptera frugiperda cell line SF21AE. Three days after transfection, the culture supernatants containing recombinant human prostasin virus were harvested and subjected to the standard plaque purification methods. Silkworm larvae at the early stage of the fifth-instar were infected with 9 × 104 plaque-forming units (PFU) of recombinant virus. On the fifth day after infection, hemolymph containing recombinant human prostasin was harvested by cutting off several abdominal legs from each larva. The hemolymph was collected in 0.1 M phosphate buffer (PB), pH 6.8 supplemented with 0.1% N-phenylthiourea. Recombinant human prostasin was purified using a Ni-sepharose column (HisTrap HP: GE Healthcare Bio-Sciences, Piscataway, NJ, USA) and an ion-exchange column (Resource Q: GE Healthcare Bio-Sciences) with an AKTA prime system (GE Healthcare Bio-Sciences). Purified recombinant prostasin was incubated with enterokinase (EK Max: Invitrogen, Carlsbad, CA, USA) for 16 h at 37 °C to generate an enzymatically active recombinant human prostasin by cleaving the enterokinase cleavage site between the light and heavy chains. Sixteen hours after incubation, enterokinase was removed from the reaction mixture by using an enterokinase removal kit (Sigma, St Louis, MO, USA). Enzymatic activity of prostasin was assessed by an assay using a synthetic substrate, N-t-Boc-Gln-Ala-Arg-7-amido-4-methyl coumarin (QAR-MCA). Application of the active recombinant prostasin significantly increased the ENaC activity in Xenopus oocytes, indicating the reliability of this recombinant protein (data not shown).
Production of antiserum
For antibody production, a partial sequence of peptide(102–120) of human prostasin, AHQLDSYSEDAKVSTLKDI, was synthesized as an octa-branching multiple antigenic peptide (Peptide Institute, Osaka, Japan) consisting of a core matrix made up of three levels of lysine and eight amino termini for anchoring peptide antigens.29 Antiserum against a synthetic prostasin peptide was generated in a rabbit by means of the lymph node injection technique.30 For immunization, 100 μg of multiple antigenic peptide was dissolved in 100 μl of saline, emulsified with an equal volume of Freund's complete adjuvant (Dibco, Detroit, MI, USA), and injected into the popliteal lymph nodes. Starting 2 weeks after the first injection, four subcutaneous injections (100 μg each) were given at multiple sites on the dorsal surface of the rabbit every 2 weeks. Blood was collected from the marginal ear vein every week, starting after subcutaneous injections had begun, and tested for antibody titer by enzyme-linked immunosorbent assay. Two weeks after the last injection, the rabbit was bled from the carotid artery. The serum was separated by centrifugation and stored at −80 °C. Before use, the antiserum was purified with a synthetic human prostasin peptide-conjugated affinity column (Affi-Gel; Bio-Rad Laboratories, Hercules, CA, USA), and the obtained antibody solution was neutralized, lyophilized and reconstructed to the volume of starting material with 0.01 M PB. The generated antibody did not show any cross-reactivity with renin, angiotensin-converting enzyme, kallikrein, prostaglandins and steroids (data not shown).
Radioiodination of human prostasin peptide
For use as a radioligand, human prostasin peptide consisting of 19 amino-acid residues was synthesized (Peptide Institute). Radioiodination was carried out at room temperature according to the modified lactoperoxidase method, as described previously.31 Briefly, Na125I (7.4 MBq, carrier free; GE Healthcare Bio-Sciences) in 2 μl of 0.1 N NaOH was added to an eppendorf tube containing 25 μl of 0.5 M PB (pH 6.9), 2.5 μg prostasin peptide in 10 μl of 0.05 M PB (pH 7.3) and 500 ng lactoperoxidase (Sigma) in 5 μl of distilled water. The reaction was started by adding 10 μl of 0.00025% H2O2. To maintain the reaction, 10 μl H2O2 was added after 1, 3 and 6 min. After 10 min of reaction, the reaction mixture was applied to a Sephadex G10 (GE Healthcare Bio-Sciences) column (12 × 0.6 cm) that had been washed with 2 ml of 1% bovine serum albumin (BSA; Sigma) in 0.05 M PB (pH 7.3) and equilibrated with 0.05 M PB (pH 7.3). Four hundred microliter aliquots were collected in tubes containing 200 μl of 1% BSA-PBS (phosphate-buffer saline) (0.01 M PB containing 0.14 M NaCl, 1% BSA and 0.1% NaN3, pH 7.5). The radioactivity of each fraction was counted in an Aloka gamma counter (AccuFLEX-γ; Aloka, Tokyo, Japan).
In this RIA system, recombinant human prostasin was used as a reference standard. RIA was performed using a double-antibody method. The prostasin antiserum diluted 1:1000 exhibited the ability to specifically bind 22% of added radioligand in the absence of any unlabeled recombinant prostasin, when 100 μl of diluted antiserum and 100 μl of labeled prostasin peptide (10 000 cpm) were added to each assay tube containing 300 μl of 1% BSA-PBS. This dilution (final dilution 1:5000) was used throughout the experiments. The RIA was carried out in disposable polystyrene tubes (10 × 50 mm evergreen; Evergreen Scientific, Los Angeles, CA, USA). The reference standard or test sample was serially diluted with the assay buffer (1% BSA-PBS, pH 7.5) and then added to assay tubes containing 200 μl of assay buffer in 100-μl volumes. The antiserum was diluted 1:1000 with 0.05 M EDTA-PBS (pH 7.5) containing 1% normal rabbit serum. One hundred microliters of diluted antibody and 100 μl of labeled prostasin peptide diluted with assay buffer were added to each tube in a total volume of 500 μl. Each preparation was assayed in duplicate. All assay tubes were incubated for 24 h at room temperature. After incubation, the immune complexes were precipitated by the addition of 200 μl of 1:100 dilution of goat anti-rabbit IgG serum (Shibayagi, Gunma, Japan) in 0.05 M EDTA-PBS containing 3.2% polyethylene glycol 6000. After incubation for 24 h at room temperature, each tube was centrifuged at 4 °C for 30 min at 3500 r.p.m., and the supernatant was aspirated. The radioactivity in each precipitate was counted in a gamma counter (Aloka). The radioactivity in tubes containing antibody and labeled prostasin peptide but no unlabeled prostasin was designated 100%, and the counts in the other tubes were expressed as a fraction of this value.
The protocol used in this study was approved by the institutional review board of Kumamoto University, and informed consent was obtained from all subjects. Twenty-six healthy volunteers, who presented BP <140/90 mm Hg and were not on any therapy, were used as a control. Subjects who were already taking antihypertensive therapy or who exhibited systolic BP and diastolic BP of 140 and 90 mm Hg, respectively, or greater were regarded as hypertensive. Hypertensive subjects with chronic kidney disease (stage 1–4) were also included, and subjects who were taking inhibitors for renin–angiotensin–aldosterone system and diuretics were excluded from our study. As most of the hypertensive subjects were being treated with antihypertensive medication, there were many subjects who exhibited systolic BP/diastolic BP less than 140/90 mm Hg. All subjects were not on salt-restricted diet. Urinary prostasin concentration was examined in 26 normotensive and 121 hypertensive subjects (20–86 years of age; 66 males and 81 females). Blood samples for aldosterone and cortisol, and urine samples for aldosterone, potassium, sodium, albumin and prostasin evaluation were also collected at the same time. These clinical parameters were measured commercially (SRL, Tokyo, Japan), and the results are summarized in Table 1.
Preparation of urine
Urine was collected in the morning and immediately chilled on ice. After measuring each urine volume, the pH was adjusted to 7.0 with 1 N NaOH; then, complete protease inhibitor cocktail (Roche Diagnostics, Tokyo, Japan) was added to inhibit the activity of endogenous proteases present in the urine. Urine was centrifuged at 4 °C for 20 min at 5000 r.p.m., filtrated through a 0.45-μm filter (Millipore, Tokyo, Japan), and concentrated by means of Centricon Plus-20 centrifuge filters (molecular weight cutoff 10 000; Millipore) with the concentration ratio between 1/2 and 1/10. The final volume was accurately measured.
Western blot analysis
Aliquots of the concentrated urine samples obtained from the human subjects were subjected to SDS-polyacrylamide gel electrophoresis in 10% polyacrylamide gels. After electrophoresis, proteins were transferred electrophoretically to Immobilon PVDF membranes (Millipore). Membranes were immunostained by the perioxidase-antiperoxidase method using a mouse monoclonal antibody against human prostasin (BD Biosciences, San Jose, CA, USA).
Statistics for linearity, parallelism, precision and potency estimation in the parallel line assay were computed according to the method of Bliss.32 Simple correlation coefficients were calculated between urinary prostasin level and plasma aldosterone or urinary aldosterone and Na/K ratio in hypertensive patients. The statistical significance of the correlation was evaluated by the method of Snedecor and Cochran.33
A specific RIA for human prostasin was developed by using a synthetic partial peptide of human prostasin for antibody production and radioligand, and a recombinant prostasin as a reference standard. The recombinant human prostasin standard resulted in a log-dose inhibition of binding of 125I-labeled prostasin peptide to the antiserum (Figure 1). The sensitivity of the RIA, defined as the amount of recombinant prostasin that significantly decreased the counts by 2 s.d. from the 100% value, averaged 55.2±11.0 ng (mean of five assays±s.e.) prostasin per 100 μl of assay buffer. The precision of the assay was determined by assaying the recombinant prostasin standard. The interassay coefficient of variation was 8.2% when the estimated dose required for 50% inhibition in five assays was used. The intra-assay coefficient of variation of 1.3% was obtained by repeated determinations using a 1563-ng recombinant prostasin standard. The linear portions of the inhibition curves obtained using seminal fluid and urine of humans paralleled the linear portion of the inhibition curve obtained with recombinant prostasin (Figure 1). To confirm the reliability of this RIA system, we compared the amount of prostasin in urine determined by the RIA with the abundance of prostasin detected by immunoblotting of the corresponding urine sample. As shown in Figure 2, each immunoassayable prostasin level (Figure 2a) corresponded to that immunoreacted with a monoclonal antibody against human prostasin (Figures 2b and c).
The RIA was applied to the determination of urinary prostasin in 26 normotensive and 121 hypertensive subjects. Urinary or plasma aldosterone levels, and other major clinical characteristics (Table 1), were also evaluated to clarify the physiological relationships among prostasin, aldosterone and ENaC function. In this study population, the values for urinary prostasin increased as the concentration of urinary aldosterone excretion increased, showing a high significant correlation (correlation coefficient: 0.673; P<0.0001) (Figure 3). As shown in Figure 4, moreover, there was a significant correlation between urinary prostasin and plasma aldosterone (correlation coefficient: 0.229; P<0.05), whereas plasma cortisol levels did not show any significant correlation with urinary aldosterone levels (correlation coefficient: 0.152; not significant (NS)). In addition, urinary prostasin excretion was inversely correlated with urinary Na/K ratio (correlation coefficient: −0.425; P<0.0001) (Figure 5), and urinary aldosterone level had a significant negative correlation with urinary Na/K ratio (correlation coefficient: −0.445; P<0.0001). We also analyzed the relationships between urinary prostasin and urinary albumin, systolic BP or diastolic BP. However, we did not see any significant correlation within these parameters (correlation coefficient: 0.140, 0.028 and 0.010, respectively; NS). The ratio of plasma aldosterone to renin activity,34 a useful screening test for the diagnosis of primary aldosteronism, was not correlated with urinary prostasin (correlation coefficient: 0.022; NS). Furthermore, renal function that is estimated by the eGFR formula had no effect on either urinary prostasin or urinary aldosterone levels (correlation coefficient: 0.044 and 0.040, respectively; NS).
This study is the first report of a clinical investigation using an RIA for human prostasin to directly assess urinary prostasin and to determine the relationship between prostasin and aldosterone levels. To date, prostasin has been detected using techniques such as immunohistochemistry and immunoblotting. More recently, Olivieri et al.20 established urinary prostasin as a possible candidate marker of ENaC activation using two-dimensional immunoblotting. The RIA that we developed for the measurement of human prostasin using a partial peptide synthesized according to the amino-acid sequence of human prostasin and a recombinant prostasin expressed in silkworm as a radioligand and a reference standard, respectively, was shown to be specific enough to measure urinary prostasin levels. Parallelism of inhibition curves between the recombinant prostasin standard and body fluids such as seminal fluid and urine indicates that the intact form of human prostasin is measurable with this RIA. However, a large amount of prostasin standard was necessary for the displacement of radioligand from the antiserum, suggesting the relatively lower sensitivity of this RIA. Yu et al.10 produced an antiserum against prostasin purified from human seminal fluid to develop an RIA for human prostasin. The value of urinary prostasin that we obtained in the present experiment was quite comparable with their value. When the same volume of urine that we used for the RIA was subjected to SDS-polyacrylamide gel electrophoresis and immunoblotting, each level of prostasin estimated with the RIA was reflected in the level of intensity of the prostasin band immunoreacted with monoclonal antibody against human prostasin.
First of all, we analyzed the relationship between prostasin and BP to identify a potential candidate for a novel marker for the pathogenesis of hypertension. In this study, however, we were unable to find an association between BP and prostasin within these samples (data not shown). The reason for this may be derived from the constantly normalized value of BP to less than 140/90 mm Hg (systolic BP/diastolic BP; 138.9±2.3/80.9±1.3 mm Hg) in most of the patients, by virtue of treatment with antihypertensive medications. Antihypertensive drugs, such as Ca channel blockers, may have a direct effect on urinary prostasin levels. Moreover, many of the subjects in this study had multiple complications including diabetes, renal failure and obesity. These metabolic factors may also have an impact on urinary prostasin levels. However, as our study size was not large enough, we were unable to analyze the influence of those drugs or complications on the urinary prostasin level.
We found that urinary prostasin had a highly significant positive correlation with urinary aldosterone levels using the RIA system. A significant positive correlation was also shown between urinary prostasin and plasma aldosterone. To our knowledge, this is the first report showing that an increase in urinary prostasin excretion is concomitant with an increase in urinary or plasma aldosterone. We previously showed the stimulatory effect of aldosterone on the substantial increase in prostasin gene expression and on the accumulation of prostasin in the culture medium of cortical collecting duct cells or urine in the rat, with functional consequences on sodium balance in vivo.19 To elucidate the source of the urinary excreted prostasin, we determined the relationship between urinary albumin and urinary prostasin. As described above, we did not detect any significant correlation between them. Therefore, we speculated that major part of the urinary prostasin was produced and secreted by the renal tubules. We also previously showed that urinary excretion of prostasin is increased in aldosterone-infused rat and in patients with primary aldosteronism, and that adrenalectomy in these patients significantly reduces urinary prostasin excretion. Recently, Olivieri et al.20 showed that there exists an aldosterone-responsive aliquot in urinary prostasin that is modulated by sodium intake and is potentially suitable as a candidate marker of ENaC activation. Our present data showing a significant negative correlation (correlation coefficient: −0.425, P<0.0001) between Na/K ratio and prostasin strongly support their observation. A negative correlation between urinary aldosterone level and urinary Na/K ratio suggest the cooperative relationship among aldosterone, prostasin and ENaC. Taken together, these findings indicate that prostasin is an important physiological regulator of sodium handling in the kidney, and that aldosterone plays a regulatory role in prostasin expression and urinary sodium and potassium balance. The RIA for urinary prostasin developed by us will be a useful tool for the non-invasive evaluation of ENaC activity in the kidney. As an increased ENaC activity is involved in some case of salt-sensitive hypertension, the measurement of urinary prostasin levels by this RIA may serve as a diagnostic tool for the salt-sensitive hypertension and for choosing an appropriate therapeutic strategy for hypertension.
In conclusion, we detected prostasin in urine from normotensive and hypertensive subjects by using an RIA for prostasin developed by us. This is the first study to show a link between urinary prostasin and urine or plasma aldosterone in humans. A concomitant increase in urinary prostasin and a decrease in urinary Na/K ratio confirm previous findings. Our findings suggest that urinary prostasin may serve as a surrogate marker for ENaC activation that leads to hypertension. However, it is not clear, at the present time, whether endogenous aldosterone regulates prostasin expression or vice versa. Further study will be required to elucidate this.
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We thank Drs Hiroyuki Fujisaki (Hirasa Clinic), Shigeru Kiyama (Kiyama-Nakamura Clinic), Yoshinori Ko (Ko Clinic), Takehiro Ko, Shiho Wakamatsu and Masataka Adachi (Kumamoto University) for sample collection. This work was supported by the following: Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology in Japan (19590956 to KK and 18390252 to KT); Salt Science Research Foundation Grant (0728 to KK); Mitsubishi Pharma Research Foundation Grant (to KK); and Suzuken Memorial Foundation Grant (to KK).
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Koda, A., Wakida, N., Toriyama, K. et al. Urinary prostasin in humans: relationships among prostasin, aldosterone and epithelial sodium channel activity. Hypertens Res 32, 276–281 (2009). https://doi.org/10.1038/hr.2009.6
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