- Open Access
Relevance of selenoprotein transcripts for selenium status in humans
© The Author(s) 2011
- Received: 5 July 2011
- Accepted: 19 August 2011
- Published: 7 September 2011
The most commonly used methods for assessing the selenium (Se) status in humans involve analysis of Se concentration, selenoprotein activity, and concentration in the blood and its compartments. Recently, it has been suggested that the expression of selenoprotein mRNA in circulating blood leukocytes could differently reflect Se status, due to prioritization of specific selenoprotein synthesis in response to dietary Se supply. Whereas the Se levels required for optimization of selenoprotein P level and plasma glutathione peroxidise activity are well known, estimation of Se level that is required for maximal mRNA expression of selenoprotein in humans is the subject of current investigations. Studies on rats suggest that whole blood selenoprotein mRNA level can be used as the relevant molecular biomarker for assessing Se status, and suboptimal Se intake may be sufficient to achieve effective expression. Human studies, however, did not confirm this hypothesis. According to studies on rodents and humans discussed in this review, it appears that suboptimal Se intake may be sufficient to satisfy molecular requirements of Se and it is lower than current recommended dietary intake in humans. The use of selenoprotein transcripts as a molecular biomarker of Se status requires further studies on a large group of healthy individuals with different baseline Se, including data regarding genetic polymorphism of selenoproteins and data regarding potential modifiers of Se metabolism.
Cellular; tissue localization
Cytosolic glutathione peroxidase (GPx)
Cytosol, mitochondria; widely expressed
Cytosol, ER; gastrointestinal tissue, liver
Secreted; plasma, extracellular fluid, liver, kidney, heart, lung, thyroid, gastrointestinal tissue, breast
Phospholipid hydroperoxide GPx
Cytosol, mitochondria, nucleus; widely expressed, testes
Unknown; embryo and oilfactory epithelium
ER, membrane protein
Selenoprotein R; methionine sulfoxide reductase B1
Cytosol, nucleus; widely expressed
Cytosol; widely expressed, brain, colon, heart, skeletal muscle, prostate
Transport and storage of Se
Secreted, cytosol; plasma, widely expressed, brain, liver, testes
Thioredoxin reductase, type I
Cytosol, nucleus; widely distributed
Thioredoxin reductase, type II
Mitochondria; widely distributed
Thioredoxin reductase, type III
Cytosol, ER, nucleus; testis-specific
Thyroid hormone metabolism
Iodothyronine deiodinase, type I
Membrane protein; kidney, liver, thyroid, brown adipose tissue
Iodothyronine deiodinase, type II
ER, membrane protein; thyroid, central nervous system, brown adipose tissue, skeletal muscle
Iodothyronine deiodinase, type III
Membrane protein; placenta, central nervous system, fetus
Selenoprotein 15 kDa
ER membrane; widely expressed
ER, membrane protein; widely expressed
Nucleus; widely expressed
The role of Se and selenoproteins in human health and diseases has been intensively studied with special attention on the determination of relevant biomarkers of Se status. The measured Se status depends mainly on dietary intakes. In the diet, Se is largely found in animal foods, and to a lesser extent also in plants, which indicates large individual differences in Se intake, associated with dietary menu composition, but also with the origin of food, which can be grown (plants) or bred (animals) on soils with different Se content (Gromadzinska et al. 2008). In humans, dietary Se intakes also vary geographically from low to high Se areas. Well documented Se deficiency health effects—Keshan and Kashin-Beck (KBD) diseases, associated with muscle disorders, were found in a broad zone running from northeast to southwest China, from the border of Heilongjiang to the Yunnan province, where concentration of Se in the soil was very low (Oldfield 1999). In European countries, dietary Se intake is lower than that observed in USA, mainly due to low Se soils. Recommended dietary intake (RDI) value of Se for adults in USA and Europe is 55 μg/day. Tolerable upper intake level determined by the US Food and Nutrition Board (NAS 2000) is 400 μg/day, while that determined by the Scientific Committee on Food in Europe is 300 μg/day (EFSA 2008). Average intake of Se by European population ranges from 27 to 70 μg per day (EFSA 2008), which is insufficient to meet the daily requirement. Clinical signs of marginal Se deficiency in Europe have not been observed or documented yet. However, it should be noted that several groups of healthy individuals may be specially prone to Se deficiency, which includes breast-fed neonates, pregnant women, and elderly people (Bellinger et al. 2009).
The relationship between Se level and health effects is represented by a U-shaped curve that suggests health pathologies associated with Se deficiency as well as its excess (Ip 1998; Jablonska et al. 2008). The altered Se status resulting from insufficient Se intake is very often associated with different diseases, including immune diseases, cardiological diseases, and cancer. On the other hand, recent studies have indicated that long-term high dietary Se supply seems to be related to the risk of type 2 diabetes, amyotrophic lateral sclerosis, and some types of cancer (Bellinger et al. 2009; Nogueira and Rocha 2011).
Although Se levels in blood and blood compartments are easily accessible markers of human Se nutritional status, Se level itself does not reflect its functional significance. Plasma or serum Se, very often used in various Se investigations, reflects rather short-term Se status, while platelet, leukocyte, and erythrocyte Se reflects its longer-term status. Two best known selenoprotein biomarkers that have been widely used in discriminating of Se status are as follows: plasma selenoprotein P (SePP1) level and plasma glutathione peroxidase (GPx3) activity. In healthy humans, plasma Se is incorporated as Sec in two selenoproteins: SePP1 (40–70%), GPx3 (20–40%), while 6–10% of Se is bound to albumin in the form of selenomethionine, through the replacement of methionine. Free Se accounts for less than 1% of total plasma Se (Vincent and Forceville 2008). These biomarkers generally reflect the major sources of human body Se, because GPx3 and SePP1 are the unique secreted selenoproteins. GPx3 is mainly synthesized in kidney, where it is produced by the cells of proximal tubular ephitelium and by parietal cells of Bowman’s capsule and then it is released into the plasma (Gromadzinska et al. 2008; Reeves and Hoffmann 2009). Mammalian SePP1 that contains multiple Sec residues (10 Sec residues in humans and rodents) is synthesized in liver and then secreted into the blood and transported to other tissues. Therefore, SePP1 serves as Se transporter and Se body distribution controller. Recently, specific apolipoprotein E receptor-2 (ApoER2) for SePP1 uptake in brain and testis and ApoER2 homolog—megalin—for SePP1 uptake in kidney proximal tubule epithelial cells were found, suggesting receptor-mediated uptake of Se in these organs (Burk and Hill 2009).
There is a growing interest in the use of transcripts level as a molecular biomarker with special regard to whole blood. Since early 1990s, research on this new molecular biomarker of Se status has been extended to Se studies in rodents, showing prioritization of preservation and degradation of specific selenoprotein mRNA under Se deficiency and under conditions of adequate and enhanced supply (Bermano et al. 1995). The observed hierarchy of the expression of selenoprotein mRNA in response to dietary Se supply has indicated the order of selenoproteins, some of them dramatically affected under Se deficiency or its excess, and others only marginally. Selenoprotein transcripts analysis in the blood gives an opportunity to obtain genomic fingerprints, in response to Se status, but also reflect an impact of genetic polymorphism of selenoproteins. In a few recent human studies, selenoprotein gene expression level in circulating human blood leukocytes was used as a longer term Se status indicator. Some other studies have been focused on the role of Se incorporation during selenoprotein synthesis under different Se dietary status in humans (Pagmantidis et al. 2008; Ravn-Haren et al. 2008a, b; Reszka et al. 2009; Sunde et al. 2008).
Levels of Se for optimization of SePP1 concentration and GPx3 activity in plasma have been determined in people living in Se-adequate areas. However, these biomarkers may be unsuitable under conditions of high Se status, because of plateau levels obtained at such concentrations. On the other hand, Se levels in blood of individuals living in low Se areas with low Se intake may be insufficient to ensure maximal activity and/or concentration of selenoproteins GPx3 and SePP1 (Thomson 2004). Therefore, determination of Se intake and Se status in humans with variable Se supply seems to be important in assessing the most sensitive Se status biomarkers. In this review, we present recent findings regarding molecular Se biomarkers, based on rodent and human studies.
Se status measured by serum/plasma Se, plasma SePP1 concentration and plasma GPx3 activity may differently respond to Se supplementation, which can give information about low, adequate, and high Se dietary intake. Since several years, it has been generally accepted that selenoprotein level and/or activity may be more useful in determining Se status than Se itself. Two human selenoproteins, GPx3, and SePP1 are believed to be good nutritional Se biomarkers in humans. Studies on Se-deficient populations showed that full expression of SePP1 required larger intake of Se than did GPx3 activity (Xia et al. 2005, 2010). Therefore, setting RDI values for Se intake was based on their assessment of the amount of Se required to achieve optimal activity or two-thirds optimal activity of GPx3 in plasma to meet the requirements of people living in low, adequate, and high Se areas (Rayman 2004).
Different chemical forms of dietary Se from animal foods and plants, such as selenite, selenocysteine, and selenomethionine, are involved in metabolic pathways to form selenide. Selenide is then transformed into Sec for selenoprotein biosynthesis or may be methylated to the main metabolite—selenosugar and then excreted with urine (Rayman 2004). Selenomethionine is a major form of organic selenium in plant foods, similarly like selenium-enriched yeast in Se supplements. Because of different metabolism of Se compounds in organism, absorption of Se from different organic and inorganic Se food sources, and Se supplements, their incorporation in selenoprotein and urinary Se excretion may vary in humans. Studies on North Americans (Burk et al. 2006) and Se-deficient Chinese subjects (Xia et al. 2005) clearly indicate that Se in the form of selenomethionine is more easily absorbed than selenite. Absorption of Se from yeast was greater than this inorganic form but less than selenomethionine. Interestingly, plasma Se seemed to reflect selenomethionine content of yeast but not the other yeast Se forms, indicating its effective bioavailability (Burk et al. 2006).
In several populations in suboptimal Se areas in Europe, China, New Zealand, concentration of SePP1 could not reach the plateau because of low Se daily intake, suggesting that Se nutritional requirements had not been achieved (Xia et al. 2005). In Se-deficient Chinese subjects, different plateaus reached by plasma GPx3 activity and plasma SePP1 level indicates that the latter is a better indicator of Se status in humans, because a larger intake of Se has been required for optimized SePP1 concentration than did GPx3 activity (Xia et al. 2010). In addition to GPx3 activity, plasma SePP1 level may be a suitable Se status and Se intake biomarker in individuals from low Se populations with additional supply of Se. In populations living in high Se areas, e.g., Australia (Queensland), USA, and Canada (central states and provinces) (Oldfield 1999), where GPx3 activity and SePP1 level in plasma can be optimized by dietary Se supply, plasma Se seems to reflect Se status and Se intake (Burk et al. 2006).
The unique conserved stem-loop Sec insertion sequence (SECIS) in the 3′-untranslated region of mammalian selenoprotein mRNA is essential for the recognition of UGA as a codon for Sec. Sec may be synthesised from different Se dietary sources: selenomethionine, selenocysteine or selenite, Se compounds which are further metabolized to selenide and then in the presence of selenophosphate synthetase 2 to selenophosphate This process requires specific Sec tRNA[Ser]Sec, several translation factors like SBP2, EFSeC, and others that serve to distinguish between UGA codons designated for Sec from those terminating translation. Sec synthesis occurs directly on its Sec tRNA[Ser]Sec, initially carrying a serine residue, which serves as an acceptor for selenophosphate. Maturation of Sec tRNA[Ser]Sec requires methylation, and two isoforms of methylated and unmethylated Sec tRNA[Ser]Sec are observed. Se supplementation is known to modulate the relative ratio between these two isoforms and promote the methylation of Sec tRNA[Ser]Sec. (Hatfield and Gladyshev 2002; Hesketh and Villette 2002; Jameson and Diamond 2004; Schomburg and Schweizer 2009; Small-Howard and Berry 2005).
It has been observed that the alterations in selenoprotein activity and concentration during Se depletion and repletion are accompanied by changes in the mRNA level. Under severe Se deficiency, this microelement is accumulated mainly in the brain and endocrine tissues, where elevated expression and activity of phospholipid glutathione peroxidase (GPx4) and thyroxine deiodinase (DIO) were observed, indicating the biological importance of these selenoproteins (Schomburg and Schweizer 2009). According to rodent studies, the main selenoproteins that are resistant to dietary Se changes are GPx4 and DIO; thioredoxine reductases (TrxR) and SePP1 are moderately sensitive, while GPx1, SelW, SelH are very sensitive to low Se supply (Reeves and Hoffmann 2009; Sunde 2010). Several in vitro and in vivo studies have shown that, under Se deficiency, the degradation of selenoprotein mRNA occurs through NMD (nonsense codon-mediated mRNA decay) (Moriarty et al. 1998; Weiss and Sunde 1998). Due to specific nucleotide sequences and preferential binding of SBP2 translation factor, 14 of 25 human selenoprotein mRNAs may be sensitive to NMD-based degradation under low Se supply (Squires et al. 2007). However, a study on rodents, suggesting regulation of selenoprotein expression, irrespective of this hypothetical preference, indicates that also other mechanisms concerning differences in the expression efficiency of some selenoproteins under Se deficiency must exist (Sunde et al. 2009). In addition, methylated Sec tRNA[Ser]Sec supports the biosynthesis of selenoproteins GPx1, GPx3, SelR, SelT, sensitive to low Se supply, while other selenoproteins, like TrxR1 and GPx4, moderately sensitive and resistant to low Se supply, require unmethylated isoform (Schomburg and Schweizer 2009).
An attempt to answer the question whether selenoprotein gene expression may be used as a biomarker of Se status was presented for the first time by Roger A. Sunde’s team. Sepp1 mRNA shows the highest expression in rat testes and liver, while Gpx3 mRNA expression is highest in rat kidney (Evenson et al. 2004), which is in agreement with observed selenoprotein activity and protein expression in these organs. Therefore, these molecular biomarkers may be also useful for the determination of Se status as well as for establishing physiological requirements of Se for adequate selenoprotein gene expression. These authors found also that, in rodents, Gpx1, Selh, and Selw mRNA levels were highly regulated by Se status (Sunde 2010). Analysis of hierarchical regulation of different selenoprotein mRNAs by Se status indicates that Gpx1 transcripts level is the best and adequate molecular biomarker in rats, because dietary Se deficiency similarly decreased Gpx1 mRNA in blood and liver. By way of comparison, decrease in Se supply in diet did not affect Gpx4 mRNA in liver and blood. Gpx1 mRNA expression in rat liver was the highest, while in blood, expression of this selenoprotein was at 4th place in tissue rank, comparable with the expression in heart and kidney. Interestingly, other investigated selenoprotein transcripts also presented distinct expression pattern across the tissues and it was found that Gpx1, Gpx3, Gpx4, Sepp1, Trxr1 expression in blood were comparable with those observed in the major organs (Evenson et al. 2004).
Regulation of selenoprotein mRNA under Se dietary deficiency presents diversity, from dramatic decrease in Gpx1 mRNA to lack of changes for Gpx4 mRNA. Low selenoprotein mRNA observed in rodents reflect depletion of Se supply in the diet, and adequate Se supply regulates expression level very efficiently. It has been found that at least half of the dietary Se necessary to provide plateau for enzymatic activity or protein expression is adequate to provide plateau for mRNA expression in liver, muscle, and kidney of rats (Barnes et al. 2009). With increasing Se level, selenoprotein mRNA level is expressed as hyperbolic curve presenting plateau breakpoints at low Se supply for majority of selenoproteins. Minimal Se requirement for growing rats was 0.1 μg Se/g diet based on liver Se, liver, and RBC GPx1 activity. Slightly lower dietary Se requirements based on plasma GPx3 activity, liver TrxR activity, and liver and kidney GPx3 activity were observed. Based on dose–response curves for selenoprotein mRNA indifferent tissues, the minimum dietary requirements were lower than for physiological Se biomarkers, ranging between 0.04 and 0.06 μg Se/g diet in liver and kidney and was between 0.03 and 0.05 μg Se/g diet in muscles. Besides, it has been assumed that it is not feasible to use selenoprotein mRNA in rat tissues as a biomarker for super-nutritional Se level (up to 0.8 μg Se/g diet). These experiments evidently suggest that marginal level of Se in diet is able to increase selenoprotein mRNA to adequate level in rats and mice, what may suggest common mechanism in regulation of selenoprotein mRNA expression by dietary Se supply (Barnes et al. 2009). Recently, Sunde (2010) proposed the panel of molecular biomarkers, which could be useful for the assessment of selenium status in rats and might be effective as the traditional biomarker panel in rat tissues. Gpx1, Gpx3, Selt, and Selw mRNA panel of transcripts level was significantly correlated with liver Se concentration, Gpx1 and Selk mRNA were associated with liver Gpx1 activity, while Sepw and Selk mRNA reflected kidney selenium status, and Gpx1, Sepw, Txnrd1 transcripts level correlated with Gpx1 kidney activity.
Interestingly, recent studies suggest that regulation of selenoprotein mRNA by Se dietary status is not a general phenomenon in rodents. It was found that in mice, majority of analyzed selenoprotein transcripts in liver and kidney were not significantly regulated by Se deficiency (Sunde et al. 2009). It has been found that minimum Se requirement of the turkey is higher than for rodents (Sunde and Hadley 2010). Dietary requirement was decreased at least 50% in old rats as compared to requirements of young animals (Sunde and Thompson 2009). Expression of the majority of selenoprotein mRNA in testis, except for Gpx1, Sepp1, Sepw, and also Apoer2, was not regulated by dietary Se status (Schriever et al. 2009). The mRNA abundances of the 12 selenoprotein genes in thyroid and pituitary of young pigs were resistant to increasing Se dietary supply in diet and also Se deficiency, but not in liver, where NMD under Se deficiency was observed for Gpx1, Sepw, Sepn, Txrd1. The testicular mRNA of Txnrd1 and Sep15 were decreased by increasing dietary Se supply, indicating that high Se status may be associated with a decrease in selenoprotein mRNA transcripts level (Zhou et al. 2009).
Differences in dietary minimal Se supply required for maximal mRNA expression and/or selenoenzyme activity suggest differential regulation depending on the type of selenoprotein as well as tissue. Therefore, findings regarding ranking of different selenoproteins synthesis within tissue and also different distribution of selenoproteins in various tissues should be considered in establishing a universal Se status biomarker (Sunde 2010).
Human studies on selenoprotein molecular biomarkers
Baseline daily Se intake (μg)
Mean ± SD
Baseline plasma Se level (ng/ml)
Mean ± SD
Selenoprotein gene expression in WBC
UK, SELGEN study, n = 39, both sexes, 6 week. Se intervention (Pagmantidis et al. 2008)
93.9 ± 1.7
Denmark, n = 20, 18–40 years. old men, 1 week Se intervention (Ravn-Haren et al. 2008a)
49.8 ± 13.6
113.2 ± 12.2
No effect: GPx1, TrxR1 SePP1
Denmark, PRECISE pilot study, n = 105, both sexes, up to 5 years. Se intervention (Ravn-Haren et al. 2008b)
49.8 ± 13.6
93 ± 11.2
No effect: GPx1
UK, n = 39, both sexes, 28 week. Se intervention (Sunde et al. 2008)
48 ± 14
89.2 ± 12.5
No effect and no association between Se status and GPx1, GPx3, GPx4, SePP1, SepW, SepH
Poland, n = 47 healthy men (Reszka et al. 2009)
24.2 ± 17.4 (unpublished data)
54.3 ± 14.6
No association between Se status and GPx1, GPx3, SePP1, Sep15
In human population, there is a large individual variation in response to Se supplementation, appearing to be unrelated with the baseline Se status (Brown et al. 2000), which may clearly indicate occurrence of selenoprotein gene variants. Recent human studies indicate that selenium status, measured as body Se, as well as SePP1 plasma level and GPx activity, may be significantly influenced by genetic polymorphism of specific selenoproteins, including GPx1 (rs1050450) (Jablonska et al. 2009), SePP1 (rs7579, rs3877899) (Meplan et al. 2007, 2009), GPx4 (rs713041) (Meplan et al. 2008). The impact of SePP1 variations in codon 234, associated with Ala to Thr change (rs3877899) and G to A transition within 3’ untranslated region (UTR) of SePP1 mRNA (rs7579), resulted in the alteration of Se status before as well as after Se supplementation (Meplan et al. 2007). These polymorphisms also influence proportion of two SePP1 50 and 60 kDa isoforms in plasma, which was proposed as the modulation factor of Se incorporation during selenoprotein synthesis (Meplan et al. 2009). Se availability modulated by SePP1 variants, resulting in difference in isoform pattern was restricted just to males. Interestingly, a possible impact of gender was observed for functional significance of GPx4 genetic polymorphism. Single nucleotide polymorphism in 3′-UTR of GPx4 mRNA, associated with C to T change (rs713041) influenced the level of GPx4 in lymphocytes, and also other selenoproteins; however, this effect was more evident in females (Meplan et al. 2008). One may hypothesize that separate molecular mechanisms for GPx4 synthesis in testes and high dietary Se requirements in males override genetic polymorphism in GPx4 and SePP1. Recent findings suggest also that the association between GPx1 activity and Se concentration, analyzed separately for each GPx1 Pro198Leu (rs1050450) genotype group, was the highest for Pro/Pro and the lowest for Leu/Leu genotype, suggesting different response of GPx1 activity to Se. This also points to the importance of the genetic background in the assessment of the Se status with the use of selenoprotein biomarkers such as GPx1 activity (Jablonska et al. 2009).
Adaptation of humans to suboptimal dietary Se supply with low Se level was observed by Finley et al. (1999) in healthy study participants living in New Zealand, where people consume less Se than suggested by the RDI of 55 μg/day. Se level in blood of individuals living in low Se areas and with low Se intake may be insufficient for maximal activity of GPx3 and level of SePP1 in plasma. However, supplementation had no effect on Se status in platelets and erythrocytes, which can be regarded as indicative of long-term Se intake. Interestingly, high retention of stable 74Se isotope in placebo individuals was observed as compared to individuals supplemented with 30 μg Se daily for 5 months, suggesting maintenance of critical Se pool in the human body and adaptation to low Se status by adjusting of its secretion. Therefore, physiological requirements of Se are lower than recommended in humans, but enabling selenoprotein synthesis. Besides, in patients with diseases like KBD and cancer, where low Se level in blood is observed, down-regulation of specific selenoprotein gene expression was found to occur in circulating WBC. Significant down-regulation of SePP1 mRNA level was observed in Han Chinese with KBD (Sun et al. 2010). In Caucasian bladder cancer male patients, SePP1, GPx1, GPx3, Sep15 mRNA levels were lower than in the control group (Reszka et al. 2009). Preferential incorporation of Sec into selenoprotein mRNA in circulating blood leukocytes under relatively low Se supply merits investigations intended to identify potential sensitive and resistant selenoproteins under Se deficiency in humans.
While the levels of Se required for optimization of SePP1 and GPx3 activities in plasma are well known, estimating Se level that is required for maximal selenoprotein gene expression in humans requires further research. According to rodents studies and studies among humans, which have been discussed in this review, it appears that suboptimal Se intake may be sufficient to achieve selenoprotein mRNA expression and molecular requirements of Se are lower than the established recommended dietary intake in humans—55 μg/day (EFSA 2008; NAS 2000). It should be noted that the expression of individual selenoprotein mRNA may be not always linked with protein expression. Therefore, since we have not understood the transcriptional and translational link of selenoprotein under different Se supply in different human tissues, biological functionality of selenoprotein could be recognized only at protein level.
Preferential incorporation of Se into selenoproteins in rodents was observed even at suboptimal dietary Se level. In rats, minimum Se requirements for achieving a plateau of selenoprotein mRNA expression have been low, reached plateau at half of the dietary Se concentration required for maximal activity of GPx1, GPx3, and maximal level of SePP1 in different tissues (Barnes et al. 2009). Therefore, in rodents, selenoprotein mRNA expression does not seem to be a good indicator for Se status. Hypothetically, in almost all populations, even in those with low and moderate Se intake and Se level in blood compartments, selenoprotein encoding gene expression might reach the plateau levels and serve as a sensitive functional biomarker of Se status. However, it should be noted that regulation of selenoprotein gene expression, metabolic pathways, and responses to Se interventions in animals may differ from those in humans. None of the human studies conducted so far has indicated that selenoprotein mRNA in the whole blood and blood cells may be a good indicator of Se status in humans (Pagmantidis et al. 2008; Ravn-Haren et al. 2008a, b; Reszka et al. 2009; Sunde et al. 2008). Low Se status may be adequate for proper regulation of selenoprotein transcription, but not for proper physiological activity of selenoproteins. Preferential incorporation of Se into selenoprotein and its optimal saturation at low dietary Se level does not provide adequate activities and selenoprotein expression in different tissues. Therefore, it may be suggested that functional rather than molecular biomarkers of Se are optimal indicators of its supply. It seems reasonable to conclude that SePP1 concentration in plasma may clearly indicate sub-optimal to optimal Se supply, because it can reflects functional significance of Se activity in organism. In over-optimal Se supply, where SePP1 level is optimized, plasma Se seems to reflect Se intake and achieved Se status.
All possible modifiers of Se status determined by means of biochemical and molecular techniques, including smoking, occupational exposure, diet, health parameters, sex, age, endocrine and immunological status, should be included, as these factors can potentially modulate selenoprotein gene expression. Impact of polymorphism of selenoproteins should be also included in complete analysis of Se requirements of individuals with different genotypes and haplotypes. Therefore, comprehensive intervention studies of circulating leukocyte selenoprotein transcript levels in a population with suboptimal and with adequate compared to over-optimal selenium status should be conducted.
This work was financially supported by the Ministry of Science and Higher Education (grant 1978/B/P01/2009/37 and 1666/B/P01/2011/40) and NIOM internal grants IMP 1.3/2007, IMP 1.8/2009. Part of this work was presented at 9th International Symposium on Selenium in Biology and Medicine. Selenium 2010, May 31–June 4 Kyoto, Japan.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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