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. 2015 May 5;113(12):1903–1910. doi: 10.1017/S0007114515001178

Placental amino acid transport may be regulated by maternal vitamin D and vitamin D-binding protein: results from the Southampton Women's Survey

J K Cleal 1,*,, P E Day 1,, C L Simner 1, S J Barton 2, P A Mahon 2, H M Inskip 2, K M Godfrey 1,2,3, M A Hanson 1,3, C Cooper 2,3,4, R M Lewis 1, N C Harvey 2,3; the SWS Study Group2
PMCID: PMC4498463  PMID: 25940599

Abstract

Both maternal 25-hydroxyvitamin D (25(OH)D) concentrations during pregnancy and placental amino acid transporter gene expression have been associated with development of the offspring in terms of body composition and bone structure. Several amino acid transporter genes have vitamin D response elements in their promoters suggesting the possible linkage of these two mechanisms. We aimed to establish whether maternal 25(OH)D and vitamin D-binding protein (VDBP) levels relate to expression of placental amino acid transporters. RNA was extracted from 102 placental samples collected in the Southampton Women's Survey, and gene expression was analysed using quantitative real-time PCR. Gene expression data were normalised to the geometric mean of three housekeeping genes, and related to maternal factors and childhood body composition. Maternal serum 25(OH)D and VDBP levels were measured by radioimmunoassay. Maternal 25(OH)D and VDBP levels were positively associated with placental expression of specific genes involved in amino acid transport. Maternal 25(OH)D and VDBP concentrations were correlated with the expression of specific placental amino acid transporters, and thus may be involved in the regulation of amino acid transfer to the fetus. The positive correlation of VDBP levels and placental transporter expression suggests that delivery of vitamin D to the placenta may be important. This exploratory study identifies placental amino acid transporters which may be altered in response to modifiable maternal factors and provides a basis for further studies.

Keywords: Vitamin D, Amino acid transporters, Placenta


Vitamin D insufficiency is common in women of childbearing age and is associated with reduced foetal growth and poor postnatal health( 1 , 2 ). The biologically inactive 25-hydroxyvitamin D (25(OH)D) is used to monitor vitamin D status, as this is the major circulating form( 3 ). In the Southampton Women's Survey (SWS), a prospective longitudinal study of maternal nutrition and lifestyle before and during pregnancy, it was found that lower maternal 25(OH)D was associated with morphological changes in the foetal femur( 4 ), lower neonatal fat mass and greater fat mass and lower grip strength in childhood( 5 , 6 ). Reduced 25(OH)D during late pregnancy was also associated with reduced bone mineral content in children at 9 years of age in another Southampton cohort study( 2 ).

The mechanisms underlying these associations are not fully understood, but are likely to involve the placenta, the sole conduit for nutrients from mother to fetus. We previously reported that placental mRNA expression of the vitamin D sensitive Ca transporter plasma membrane Ca ATPase 3 (PMCA3) and the imprinted gene Pleckstrin homology-like domain family A member 2 (PHLDA2) is associated with offspring bone mass development and composition( 7 , 8 ). Other than Ca transport, a key element for foetal bone development is placental amino acid transport. Placental amino acid transfer is vital for foetal growth( 9 ), and animal studies suggest that decreased amino acid transport precedes foetal growth restriction( 10 ). Amino acid transfer to the fetus involves amino acid transport across the microvillous and basal membranes of the placental syncytiotrophoblast( 11 ) and potentially metabolic interconversion within the placenta( 12 ). Placental amino acid transfer is thought to be regulated by maternal nutritional and hormonal factors( 13 15 ).

There are three classes of amino acid transporter in the human placenta; accumulative transporters, amino acid exchangers( 16 , 17 ) and facilitated transporters( 18 ) (Fig. 1). Accumulative transporters mediate net uptake of specific amino acids across the microvillous membrane (e.g. SNAT), and also play roles on the basal membranes such as uptake of foetal glutamate for placental glutamine synthesis (e.g. EAAT)( 12 ). The exchangers including LAT, y+LAT and ASCT use the gradients built up by accumulative transporters to drive uptake and transfer of other amino acids including many essential amino acids( 18 ). The facilitated transporters TAT1, LAT3 and LAT4 are essential for net amino acid transport to the fetus, and their gene expression in human placenta is associated with measures of foetal growth( 18 ). The factors that regulate these changes in gene expression are not understood. However, as these and several other amino acid transporters have vitamin D response elements (VDRE) in their promoter regions, they could theoretically be regulated at the transcriptional level by maternal vitamin D. Specifically, the biologically active 1,25 dihydroxyvitamin D regulates transcription of specific genes by binding the vitamin D receptor and interacting with VDRE in their promoter regions( 19 , 20 ).

Fig. 1.

Fig. 1

Transport of amino acids across the placental syncytiotrophoblast. Amino acids are transported across the microvillous membrane (MVM) into the placental syncytiotrophoblast by active accumulative transporters (Ac; e.g. SNAT) and exchangers (X; e.g. ASCT). Amino acids transported by accumulative transporters (aaA) are then exchanged back for those only transported by exchangers (aaB). Amino acids are transported out of the placenta across the basal membrane (BM) by facilitated transporters (TAT1, LAT3 and LAT4) and exchangers (X). The facilitated transporters transport specific amino acids (aa1) down their concentration gradient to the fetus. In order to transport other amino acids (aa2) to the fetus, aa1 must be exchanged for aa2 via exchangers (X).

We therefore investigated whether maternal 25(OH)D and vitamin D binding protein (VDBP) concentrations during pregnancy are related to gene expression of the amino acid transporters, essential for placental amino acid transfer. We used samples collected from a population based cohort, the SWS.

Methods

The study was conducted according to the guidelines in the Declaration of Helsinki, and the Southampton and South West Hampshire Research Ethics Committee approved all procedures (276/97, 307/97, 089/99, 153/99, 005/03/t, 06/Q1702/104). Written informed consent was obtained from all participating women and by parents or guardians with parental responsibility on behalf of their children.

Maternal measurements

We used data and samples from the SWS, a cohort study of 3158 pregnancies with information collected from the mothers before conception( 21 ). Non-pregnant women aged 20–34 years were recruited via their general practitioners; assessments of lifestyle, diet and anthropometry were performed by trained research nurses at study entry and then in early (11 weeks) and late (34 weeks) gestation among those women who became pregnant. Subscapular skinfold thicknesses were measured to the nearest 0·1 mm in triplicate using Harpenden skinfold callipers (Baty International)( 22 ).

At 34 weeks of gestation, a maternal venous blood sample was obtained and an aliquot of maternal serum was frozen at − 80°C. Serum 25(OH)D and VDBP concentrations were analysed by RIA (DiaSorin). The 25(OH)D assay measures both 25-hydroxyvitamin D2 and 25-hydroxyvitamin D3. The detection range for this 25(OH)D assay is 3·8–250 nmol/l. The assays met the requirements of the UK National Vitamin D External Quality Assurance Scheme, and intra- and inter-assay CV were < 10 %.

Placental samples

Placentas were collected from term pregnancies within 30 min of delivery, and no clinical conditions such as pre-eclampsia or gestational diabetes. Placental weight was measured after removing blood clots, cutting the umbilical cord flush with its insertion into the placenta, trimming away surrounding membranes and removing the amnion from the basal plate. To ensure that the samples collected were representative of the placentas as a whole, five villous tissue samples were selected using a stratified random sampling method, and stored at − 80°C. For the present study, a cohort of 102 placentas was selected from 300 collected in total, based on availability of neonatal dual-energy X-ray absorptiometry (DXA) data.

RNA extraction and complementary DNA synthesis

For each placenta five snap frozen samples were pooled and powdered in a frozen tissue press. Total RNA was extracted from 30 mg powdered placental tissue using the RNeasy fibrous tissue RNA isolation mini kit (Qiagen) according to the manufacturer's instructions. The integrity of total RNA was confirmed by agarose gel electrophoresis.

Total RNA (0·2 μg) was reverse transcribed with 0·5 μg random hexamer primer, 200 units Moloney murine leukaemia virus reverse transcriptase, 25 units recombinant RNasin ribonuclease inhibitor and 0·5 mm each of deoxyadenosine triphosphate, deoxycytidine triphosphate, deoxyguanosine triphosphate and deoxythymidine triphosphate in a final reaction volume of 25 μl in 1 ×  Moloney murine leukaemia virus reaction buffer (Promega). All 102 samples were produced in one batch to reduce variation.

Probe and primer design

Intron spanning oligonucleotide probes and primers were designed using the Roche ProbeFinder version 2.45 for human. Probes were supplied by Roche from the human universal probe library and primers were synthesised by Eurogentec. Control genes were selected using the geNorm™ human Housekeeping Gene Selection Kit (Primer Design Limited).

Target genes

The genes measured in the present study along with primer and probe details are listed in Table 1. And mRNA levels were measured using quantitative real-time PCR using a Roche LightCycler 480. For Roche universal probe library probes the cycle parameters were 95°C for 10 min, followed by forty cycles of 95°C for 15 s and 60°C for 1 min. For the primer design Perfect Probes, the cycle parameters were 95°C for 10 min, followed by forty cycles of 95°C for 10 s and 60 and 72°C for 15 s. Intra-assay CV's for each gene were 5–8 %. Each of the 102 samples was run on the same plate in triplicate. All mRNA levels are presented relative to the geometric mean of the three control genes, tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide (YWHAZ), ubiquitin C (UBC) and topoisomerase (TOP1)( 23 ).

Table 1.

Information on genes, primers and probes

Transporter Gene Gene ID Genebank accession no. Primers Roche universal probe library no.
ASCT1 SLC1A4 6509 NM_003038.2 F: 5′-tttgcgacagcatttgctac-3′ 78
R: 5′-gcacttcatcatagagggaagg-3′
ASCT2 SLC1A5 6510 NM_005628.2 F: 5′-gaggaatatcaccggaacca-3′ 43
NM_001145144.1 R: 5′-aggatgttcatcccctcca-3′
EAAT1 SLC1A3 6507 NM_004172.4 F: 5′-ttgaactgaacttcggacaaatta-3′ 76
R: 5′-attccagctgccccaatact-3′
EAAT2 SLC1A2 6506 NM_004171.3 F: 5′-aaaatgctcattctccctctaatc-3′ 78
R: 5′-gccactagccttagcatcca-3′
EAAT3 SLC1A1 6505 NM_004170.4 F: 5′-agttgaatgacctggacttgg-3′ 9
R: 5′-gcagatgtggccgtgatac-3′
EAAT4 SLC1A6 6511 NM_005071.1 F: 5′-tgcagatgctggtgttacct-3′ 19
R: 5′-gttgtccagggatgccata-3′
EAAT5 SLC1A7 6512 NM_006671.4 F: 5′-cgcccaggtcaacaactac-3′ 9
R: 5′-gctgcagtggctgtgatact-5′
LAT1 SLC7A5 8140 NM_003486.5 F: 5′-gtggaaaaacaagcccaagt-3′ 25
R: 5′-gcatgagcttctgacacagg-3′
LAT2 SLC7A8 23428 NM_182728.1 F: 5′-ttgccaatgtcgcttatgtc-3′ 17
NM_012244.2 R: 5′-ggagcttctctccaaaagtcac-3′
LAT3 SLC43A1 8501 NM_003627.5 F: 5′-gccctcatgattggctctta-3′ 29
NM_001198810.1 R: 5′-ccggcatcgtagatcagc-3′
LAT4 SLC42A2 124935 NM_001284498.1 F: 5′-acaagtatggcccgaggaa-3′ 3
NM_152346.2 R: 5′-gcaatcagcaagcaggaaa-3′
SNAT1 SLC38A1 81539 NM_030674.3 F: 5′-attttgggactcgcctttg-3′ 47
NM_001077484.1 R: 5′-agcaatgtcactgaagtcaaaagt-3′
SNAT2 SLC38A2 54407 NM_018976.3 F: 5′-cctatgaaatctgtacaaaagattgg-3′ 9
R: 5′-ttgtgtacccaatccaaaacaa-3′
SNAT4 SLC38A4 55089 NM_018018.4 F: 5′-tgttctggtcatccttgtgc-3′ 29
NM_001143824.1 R: 5′-aaaactgctggaagaataaaaatcag-3′
TAT1 SLC16A10 117247 NM_018593.4 F: 5′-ggtgtgaagaaggtttatctacagg-3′ 6
R: 5′-agggccccaaagatgcta-3′
y+LAT1 SLC7A7 9056 NM_001126105.1 F: 5′-acactgccgtgagaacctg-3′ 72
NM_001126106.1 R: 5′-aggagaggaaacccttcacc-3′
y+LAT2 SLC7A6 9057 NM_001076785.1 F: 5′-gctgtgatcccccatacct-3′ 66
NM_003983.4 R: 5′-ggcacagttcacaaatgtcag-3′
4F2HC SLC3A2 6520 NM_001012661.1 F: 5′-tggttctccactcaggttga-3′ 49
R: 5′-cagccaaaactccagagcat-3′

SLC, solute carrier; F, forward; R, reverse; 4F2HC, type-II membrane glycoprotein heavy chain.

Postnatal measurements

At birth (n 102) and 4 years of age (n 42–46) a whole-body DXA scan was obtained using a Hologic Discovery instrument (Hologic, Inc.) in paediatric scan mode (Apex 3.1 software), yielding fat mass, lean mass and bone mineral content. The CV for body composition analysis with the DXA instrument was 1·4–1·9 %.

Statistics

Maternal and placental mRNA data that were not normally distributed were transformed logarithmically. Previous data showed that gene expression of the control genes and many of the target genes was higher in male than in female placentas( 24 ). Adjustment was therefore made for sex in the correlation analysis between mRNA and all other variables. Pearson's correlation coefficient (r p) was used to determine partial correlations adjusted for sex and gestational age between placental mRNA levels, neonatal body composition and maternal factors (IBM SPSS Statistics 20). The partial correlation between placental gene expression and maternal vitamin D measures was also adjusted for potential confounding factors: maternal sum of skinfold thickness, walking speed, parity and smoking during pregnancy. A value of P< 0·05 was accepted as statistically significant, and, given the observational nature of the study together with the substantial co-linearity among both predictors and outcomes, testing for multiple comparisons was felt to be inappropriate( 25 ).

Results

Characterisation of the subjects from the Southampton Women's Survey cohort

The mean age of the 102 mothers at the birth of their children was 30·9 (sd 3·9) years; 37·9 % were primiparous. 97 % of the women were of white European ethnicity. The median gestational age was 39·6 (inter-quartile range 38·8–40·7) weeks. The mean placental/foetal weight ratio was 0·13 (sd 0·02). Of the 102 placentas from SWS pregnancies studied here, fifty-three of the infants were male, forty-nine were female. The mean birth weight for males was 3547 (sd 417) g with 95 % between the 33rd and 51st centile based on UK growth charts. The mean birth weight for females was 3455 (sd 489) g with 95 % between the 36th and 59th centile.

Maternal plasma vitamin D and placental gene expression

The 34-week plasma 25(OH)D levels were measured for ninety-one of the 102 women and VDBP levels for eighty-five of the 102 women. The mean 25(OH)D levels were 71·7 (sd 32·1) nmol/l with a range of 20–158 nmol/l. The mean VDBP levels were 5622 (sd 806) mg/l with a range of 4160–8570 mg/l. Of the women, 28·6 % were taking vitamin D supplements of 10 μg/d (400 IU/d). The mean vitamin D intake (from FFQ and data on supplements) from the ninety-eight available (out of 102) women's diets is 3·5 μg/d (ranging from 1·3 to 9·0 μg/d).

Of the genes investigated mRNA for EAAT1, EAAT4 and EAAT5 were not detected in human placenta.

In this subset of SWS woman, there was a positive correlation between maternal 34-week plasma 25(OH)D levels and the mRNA expression of LAT3 (Fig. 2), ASCT1 and y + LAT1, and a negative correlation with SNAT1 (Table 2). Maternal VDBP levels correlated positively with mRNA expression of TAT1, LAT3, LAT4, SNAT1, SNAT2, y + LAT2, type-II membrane glycoprotein heavy chain (4F2HC), and EAAT3, and there was a trend with LAT1 (Table 2).

Fig. 2.

Fig. 2

LAT3 mRNA expression is associated with postnatal body composition. LAT3 relative mRNA expression in human placenta is positively correlated with maternal 25-hydroxyvitamin D (25(OH)D) (r p 0·31, P= 0·003, n 102) (a) and lean mass at 4 years of age (r p 0·38, P= 0·01, n 46) (b).

Table 2.

The associations between placental amino acid transporter mRNA expression and maternal serum 25-hydroxyvitamin D and vitamin D binding protein levels

34-week vitamin D (nmol/l) Vitamin D binding protein (mg/l) 34-week vitamin D (nmol/l) Vitamin D binding protein (mg/l)
r P r P r P r P
TAT1 0·07 0·50 0·23* 0·03* 0·14 0·21 0·12* 0·10*
LAT3 0·31* 0·003* 0·22* 0·04* 0·37* 0·003* 0·22* 0·05*
LAT4 − 0·12 0·25 0·28* 0·01* − 0·13 0·26 0·28* 0·01*
SNAT1 − 0·23* 0·03* 0·25* 0·02* − 0·20* 0·07* 0·23* 0·05*
SNAT2 0·01 0·96 0·23* 0·03* 0·04 0·70 0·23* 0·04*
SNAT4 0·14 0·19 0·08 0·45 0·12 0·30 0·12 0·29
ASCT1 0·23* 0·03* 0·06 0·62 0·20* 0·07* 0·11 0·33
ASCT2 0·04 0·74 0·18 0·10 0·05 0·63 0·17 0·14
y+LAT1 0·31* 0·003* 0·03 0·81 0·36* 0·001* 0·02 0·99
y+LAT2 0·04 0·73 0·26* 0·02* − 0·08 0·94 0·33* 0·003*
EAAT2 0·12 0·26 − 0·07 0·53 0·06 0·56 − 0·01 0·91
EAAT3 0·09 0·39 0·30* 0·01* 0·12 0·24 0·29* 0·009*
LAT1 − 0·14 0·19 0·21* 0·06* − 0·17 0·12 0·23* 0·04*
LAT2 − 0·08 0·44 0·18 0·10 − 0·07 0·54 0·17 0·14
4F2HC − 0·12 0·26 0·25* 0·02* − 0·08 0·48 0·23* 0·04*
Adjusted for sex and dGA Adjusted for sex, dGA and maternal confounding factors

4F2HC, type-II membrane glycoprotein heavy chain; dGa, days gestational age.

*P< 0·05.

When the correlation was also adjusted for maternal confounding factors (maternal sum of skinfold thickness, walking speed, parity and smoking during pregnancy) all correlations were still present, except for the relationships between 25(OH)D and ASCT1, and VDBP and TAT1, which were no longer statistically significant at the P< 0·05 level (Table 2). The adjusted data also showed a positive association between VDBP and LAT1 mRNA (Table 2).

Neonatal body composition

At birth, there were no significant associations between placental amino acid transporter gene expression and neonatal lean mass, fat mass, or bone mineral content (data not shown).

At 4 years of age total lean mass was positively associated with LAT3 (Fig. 2), y + LAT1 and TAT1 mRNA expression (Table 3). Bone mineral density was positively associated with LAT4 mRNA and negatively associated with ASCT2 and EAAT3 mRNA expression (Table 3). EAAT3 mRNA expression levels (n 42) were also negatively associated with bone mineral content (r p − 0·46, P= 0·003) and total bone area (cm2 without heads; r p − 0·43, P= 0·01). SNAT4 (r p − 0·40, P= 0·01) and y + LAT2 (r p − 0·32, P= 0·04) expression levels were negatively associated with total bone area.

Table 3.

The associations between placental amino acid transporter mRNA expression and 4-year-old dual-energy X-ray absorptiometry (DXA) measurements of body composition

Total lean (kg) (n 46) Total Prentice BMD (g), without heads (n 42)
4 year DXA r P r P
TAT1 0·33* 0·03* − 0·17 0·28
LAT3 0·38* 0·01* − 0·15 0·33
LAT4 − 0·09 0·57 0·41* 0·01*
SNAT1 − 0·12 0·45 0·06 0·72
SNAT2 0·06 0·68 − 0·11 0·49
SNAT4 0·08 0·62 − 0·18 0·26
ASCT1 0·23 0·13 − 0·27 0·09
ASCT2 0·24 0·11 − 0·42* 0·01*
y+LAT1 0·31* 0·04* − 0·25 0·11
y+LAT2 0·20 0·18 − 0·27 0·09
EAAT2 0·28 0·07 0·04 0·82
EAAT3 − 0·04 0·80 − 0·59* 0·00 005*
LAT1 − 0·21 0·16 0·09 0·59
LAT2 − 0·04 0·82 − 0·02 0·90
4F2HC 0·05 0·73 0·14 0·38

BMD, bone mineral density; 4F2HC, type-II membrane glycoprotein heavy chain.

*P< 0·05.

Discussion

Many genes related to placental function may be regulated directly or indirectly by vitamin D. The present study aimed to establish whether there are relationships between maternal vitamin D levels and changes in gene expression in placentas from the SWS. Maternal 25(OH)D and VDBP levels were positively associated with placental expression of genes involved in amino acid transport. This suggests that maternal vitamin D status may regulate the expression of placental amino acid transporters, and potentially influence the transfer of amino acids to the fetus and subsequent foetal growth. The observations that VDBP was associated with the expression of twice as many genes as vitamin D suggests that delivery of vitamin D to the placenta may be a crucial determinant of vitamin D activity. The associations seen may however, involve a more complex relationship between maternal vitamin D status and maternal body composition.

Vitamin D

Placental amino acid transport is important for foetal growth and development, so understanding how the amino acid transporters are regulated in the placenta will help us understand the mechanisms underlying foetal growth restriction and the associated postnatal phenotype. Maternal vitamin D status has also been shown to associate with both foetal and neonatal growth, and, taken with the fact that it modulates gene transcription; this suggests there may be an interaction between vitamin D and placental amino acid transport. This interaction could be a direct effect of vitamin D, and its receptor acting directly on the placental amino acid transporter genes at a VDRE or an indirect effect mediated via vitamin D's activation of another gene. Both the LAT3 and ASCT1 genes have been shown to have VDRE in their promoter region( 26 ), which could underlie the association between their mRNA expression and maternal 25(OH)D levels. Vitamin D can also down-regulate gene expression via vitamin D receptor, blocking the activity of the cyclic AMP response element in the promoter( 27 ). This may explain the observed negative association between 25(OH)D and SNAT1 mRNA expression, a gene regulated by cyclic AMP at the cyclic AMP response element( 28 ). Vitamin D can also directly affect gene transcription by an interaction between vitamin D receptor and histone acetyltransferases, leading to an open/active chromatin state( 29 ). The amino acid transporter genes could therefore be in a region of DNA, affected by vitamin D-mediated epigenetic changes, or could be regulated indirectly via an effect on another gene in the placenta.

The relationship between vitamin D and placental function may be more complex than vitamin D receptor-mediated changes in placental gene expression, and could be very indirect via an effect on maternal physiology or metabolism. It could be that vitamin D levels are influencing aspects of the maternal environment, which in turn regulate placental gene expression. Alternatively, maternal factors could simply be regulating both vitamin D levels and placental amino acid transporter expression in a similar manner. Plasma vitamin D status is known to be related to factors such as maternal smoking, parity and BMI( 30 ). It could be that maternal body composition is influencing the placenta, as a signal reflecting the mother's nutrient reserves and capacity to support the pregnancy. We have previously demonstrated an association between maternal muscle mass and placental amino acid transfer, indicating that maternal body composition can affect placental amino acid handling( 31 ).

Vitamin D levels could therefore be a proxy for another aspect of the maternal environment, and not a direct mediator of amino acid transporter expression levels. When we corrected our correlation analysis to adjust for maternal factors, we did indeed see that the amino acid transporters ASCT1 and SNAT1 were no longer related to the maternal 25(OH)D levels. These transporters may therefore be regulated by aspects of maternal body composition rather than vitamin D status, or vitamin D levels may be mediating the effects of body composition on the placenta. LAT3 and y + LAT1 did still show strong associations with maternal 25(OH)D levels, suggesting that it is the vitamin D rather than body composition that affects their regulation. Further studies are needed to establish the mechanisms underlying this association.

Interestingly, there were a number of positive associations between VDBP and amino acid transporter expression levels. This suggests that the delivery of the vitamin D to the placenta by its binding protein may be an important determinant of vitamin D action, possibly mediated by receptor-mediated endocytosis( 32 ). Further investigation into the uptake of vitamin D and levels of the active 1,25 dihydroxyvitamin D within the placenta is needed. This will help us understand and improve the effects of 25(OH)D supplementation during pregnancy, which may also require the VDBP to be upregulated.

Postnatal outcome

We previously reported that placental TAT1 and LAT3 mRNA expression levels in this cohort are positively related to measures of foetal growth, with TAT1 mRNA being associated with foetal growth in terms of lean mass( 18 ). Consistent with these observations we found that y + LAT1, TAT1 and LAT3 mRNA expression in placentas are positively related to 4-year-old lean mass. As lean mass contains a high proportion of muscle, a protein-rich tissue, its growth will require a substantial amino acid supply, and so it may rely on appropriate amino acid supply in early development.

Limitations

The present study has the advantage of using a well characterised population representative of the general population, with detailed phenotyping of mother–offspring pairs. The placentas and offspring included in this study were of the mothers who allowed DXA measurements to be undertaken. The women whose offspring had DXA measures, compared to those that did not, were slightly older and tended to be better educated. They do represent a wide range of maternal age and family backgrounds, and all comparisons were internal to the selected subset. When comparing the vitamin D levels in the women with placental samples v. the whole cohort they look very similar with a slightly higher mean, but a similar standard deviation; 71·7 (sd 32·1) nmol/l, n 91 v. 64·2 (sd 30·9) nmol/l, n 2178. In the present study we were only able to measure the inactive 25(OH)D, which is thought to be the best measure of vitamin D status. Further studies would be enhanced by measuring the level of active 1,25 dihydroxyvitamin D within the placental tissue, and relating this directly to gene expression. The exploratory nature of the present study, small sample size and the possibility of chance findings need to be acknowledged. In particular, we had reduced numbers at 4 years of age (42–46 mother–offspring pairs) due to participants' not returning for measurement. The measures made in this sub-set at 4 years of age were representative of the whole cohort, for example the mean lean mass was 11·8 (sd 1·6) kg, n 46 compared to 12·0 (sd 1·5) kg, n 743. These numbers did, however, give us greater than 90 % power to detect a correlation coefficient of 0·5. Compared to adults, DXA assessment of body composition in children is more problematic due to their smaller size and tendency to move. These DXA measures were, however, validated previously in piglets using biochemical assessment of carcass N content and lipid extraction to determine lean and fat mass, respectively( 33 ). In the present study specific paediatric software was used, and movement artefacts were minimal. While the present study focused on the actions of vitamin (as a transcription factor) on the expression of key placental genes, it would also have been interesting to study the effect of a wider range of factors including maternal and foetal amino acid levels. It is important to remember that the regulation of gene function and physiology are complex and will rarely be dependent on a single factor. It is not possible in this observational study to determine whether the observed associations are causal. Nevertheless, the patterns of observations are indicative of a role for vitamin D in the regulation of placental amino acid transporter expression, and it forms, we think, the basis for future studies.

Conclusion

In conclusion the present study demonstrates relationships between maternal vitamin D levels, and in particular VDBP and placental gene expression. As there are associations between vitamin D and body composition, these observations provide a possible mechanism by which maternal factors influence placental function. Further work needs to be undertaken to investigate the association between maternal VDBP and placental gene expression, and whether these are direct or indirect effects.

Acknowledgements

We thank the mothers who gave us their time, and the team of dedicated research nurses and ancillary staff for their assistance. We thank Mrs G. Strange and Mrs R. Fifield for helping prepare the manuscript.

This work was supported by grants from the Medical Research Council (MC_US_A620_0033), British Heart Foundation (RG/07/009), Arthritis Research UK, National Osteoporosis Society, International Osteoporosis Foundation, Cohen Trust, NIHR Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton NHS Foundation Trust, and NIHR Musculoskeletal Biomedical Research Unit, University of Oxford. Participants were drawn from a cohort study funded by the Medical Research Council and the Dunhill Medical Trust. The research leading to these results has also received funding from the European Union's Seventh Framework Programme (FP7/2007–13), project EarlyNutrition under grant agreement no. 289346. The Pump Priming Grant from The British Medical Ultrasound Society was used for the vitamin D assays carried out by Professor R. Swaminathan at King's College London.

None of the funding agencies had, however, any role to play in the research design, analyses, interpretation, findings or the reporting of the present investigation.

The authors' contributions are as follows: J. K. C., R. M. L., C. L. S. and N. C. H. formulated the specific research question and the design of the study. H. M. I., K. M. G., M. A. H., C. C., N. C. H. and the SWS Study Group designed the cohort (SWS) study. The experiments were carried out by P. E. D., J. K. C., R. M. L. and P. A. M. J. K. C. and S. J. B. analysed the data. The article was written by J. K. C., P. E. D., R. M. L. and N. C. H. with input from all other authors. The final manuscript was read and approved by all the authors.

There are no conflicts of interest.

Abbreviations: 25(OH)D, 25-hydroxyvitamin D; DXA, dual-energy X-ray absorptiometry; SWS, Southampton Women's Survey; VDBP, vitamin D binding protein; VDRE, vitamin D response element

References

  • 1. Harvey NC, Javaid MK, Poole JR, et al. (2008) Paternal skeletal size predicts intrauterine bone mineral accrual. J Clin Endocrinol Metab 93, 1676–1681. [DOI] [PubMed] [Google Scholar]
  • 2. Javaid MK, Crozier SR, Harvey NC, et al. (2006) Maternal vitamin D status during pregnancy and childhood bone mass at age 9 years: a longitudinal study. Lancet 367, 36–43. [DOI] [PubMed] [Google Scholar]
  • 3. Holick MF, Binkley NC, Bischoff-Ferrari HA, et al. (2011) Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 96, 1911–1930. [DOI] [PubMed] [Google Scholar]
  • 4. Mahon P, Harvey N, Crozier S, et al. (2010) Low maternal vitamin D status and fetal bone development: cohort study. J Bone Miner Res 25, 14–19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Crozier SR, Harvey NC, Inskip HM, et al. (2012) Maternal vitamin D status in pregnancy is associated with adiposity in the offspring: findings from the Southampton Women's Survey. Am J Clin Nutr 96, 57–63. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Harvey NC, Moon RJ, Sayer AA, et al. (2014) Maternal antenatal vitamin D status and offspring muscle development: findings from the Southampton Women's Survey. J Clin Endocrinol Metab 99, 330–337. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Lewis RM, Cleal JK, Ntani G, et al. (2012) Relationship between placental expression of the imprinted PHLDA2 gene, intrauterine skeletal growth and childhood bone mass. Bone 50, 337–342. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Martin R, Harvey NC, Crozier SR, et al. (2007) Placental calcium transporter (PMCA3) gene expression predicts intrauterine bone mineral accrual. Bone 40, 1203–1208. [DOI] [PubMed] [Google Scholar]
  • 9. Cetin I (2003) Placental transport of amino acids in normal and growth-restricted pregnancies. Eur J Obstet Gynecol Reprod Biol 110, S50–S54. [DOI] [PubMed] [Google Scholar]
  • 10. Jansson N, Pettersson J, Haafiz A, et al. (2006) Down-regulation of placental transport of amino acids precedes the development of intrauterine growth restriction in rats fed a low protein diet. J Physiol 576, 935–946. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Cleal JK & Lewis RM (2008) The mechanisms and regulation of placental amino acid transport to the human foetus. J Neuroendocrinol 20, 419–426. [DOI] [PubMed] [Google Scholar]
  • 12. Day PE, Cleal JK, Lofthouse EM, et al. (2013) Partitioning of glutamine synthesised by the isolated perfused human placenta between the maternal and fetal circulations. Placenta 34, 1223–1231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Ericsson A, Hamark B, Jansson N, et al. (2005) Hormonal regulation of glucose and system A amino acid transport in first trimester placental villous fragments. Am J Physiol Regul Integr Comp Physiol 288, R656–R662. [DOI] [PubMed] [Google Scholar]
  • 14. Jansson N, Greenwood SL, Johansson BR, et al. (2003) Leptin stimulates the activity of the system A amino acid transporter in human placental villous fragments. J Clin Endocrinol Metab 88, 1205–1211. [DOI] [PubMed] [Google Scholar]
  • 15. Shibata E, Powers RW, Rajakumar A, et al. (2006) Angiotensin II decreases system A amino acid transporter activity in human placental villous fragments through AT1 receptor activation. Am J Physiol Endocrinol Metab 291, E1009–E1016. [DOI] [PubMed] [Google Scholar]
  • 16. Cleal JK, Brownbill P, Godfrey KM, et al. (2007) Modification of fetal plasma amino acid composition by placental amino acid exchangers in vitro . J Physiol 582, 871–882. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Lewis RM, Glazier J, Greenwood SL, et al. (2007) l-Serine uptake by human placental microvillous membrane vesicles. Placenta 28, 445–452. [DOI] [PubMed] [Google Scholar]
  • 18. Cleal JK, Glazier JD, Ntani G, et al. (2011) Facilitated transporters mediate net efflux of amino acids to the fetus across the basal membrane of the placental syncytiotrophoblast. J Physiol 589, 987–997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. MacDonald PN, Haussler CA, Terpening CM, et al. (1991) Baculovirus-mediated expression of the human vitamin D receptor. Functional characterization, vitamin D response element interactions, and evidence for a receptor auxiliary factor. J Biol Chem 266, 18808–18813. [PubMed] [Google Scholar]
  • 20. Terpening CM, Haussler CA, Jurutka PW, et al. (1991) The vitamin D-responsive element in the rat bone Gla protein gene is an imperfect direct repeat that cooperates with other cis-elements in 1,25-dihydroxyvitamin D3-mediated transcriptional activation. Mol Endocrinol 5, 373–385. [DOI] [PubMed] [Google Scholar]
  • 21. Inskip HM, Godfrey KM, Robinson SM, et al. (2006) Cohort profile: The Southampton Women's Survey. Int J Epidemiol 35, 42–48. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Harrison G, Buskirk E, Carter J, et al. (1988) Skinfold thicknesses and measurement technique. In Anthropometric Standardization Reference Manual, pp. 55–70. Champaign, IL: Human Kinetics Books. [Google Scholar]
  • 23. Cleal JK, Day P, Hanson MA, et al. (2009) Measurement of housekeeping genes in human placenta. Placenta 30, 1002–1003. [DOI] [PubMed] [Google Scholar]
  • 24. Cleal JK, Day PL, Hanson MA, et al. (2010) Sex differences in the mRNA levels of housekeeping genes in human placenta. Placenta 31, 556–557. [DOI] [PubMed] [Google Scholar]
  • 25. Schulz KF & Grimes DA (2005) Multiplicity in randomised trials I: endpoints and treatments. Lancet 365, 1591–1595. [DOI] [PubMed] [Google Scholar]
  • 26. Wang TT, Tavera-Mendoza LE, Laperriere D, et al. (2005) Large-scale in silico and microarray-based identification of direct 1,25-dihydroxyvitamin D3 target genes. Mol Endocrinol 19, 2685–2695. [DOI] [PubMed] [Google Scholar]
  • 27. Yuan W, Pan W, Kong J, et al. (2007) 1,25-Dihydroxyvitamin D3 suppresses renin gene transcription by blocking the activity of the cyclic AMP response element in the renin gene promoter. J Biol Chem 282, 29821–29830. [DOI] [PubMed] [Google Scholar]
  • 28. Ogura M, Taniura H, Nakamichi N, et al. (2007) Upregulation of the glutamine transporter through transactivation mediated by cAMP/protein kinase A signals toward exacerbation of vulnerability to oxidative stress in rat neocortical astrocytes. J Cell Physiol 212, 375–385. [DOI] [PubMed] [Google Scholar]
  • 29. Karlic H & Varga F (2011) Impact of vitamin D metabolism on clinical epigenetics. Clin Epigenetics 2, 55–61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Vimaleswaran KS, Berry DJ, Lu C, et al. (2013) Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts. PLoS Med 10, e1001383. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Lewis RM, Greenwood SL, Cleal JK, et al. (2010) Maternal muscle mass may influence system A activity in human placenta. Placenta 31, 418–422. [DOI] [PubMed] [Google Scholar]
  • 32. Nykjaer A, Dragun D, Walther D, et al. (1999) An endocytic pathway essential for renal uptake and activation of the steroid 25-(OH) vitamin D3 . Cell 96, 507–515. [DOI] [PubMed] [Google Scholar]
  • 33. Brunton JA, Weiler HA & Atkinson SA (1997) Improvement in the accuracy of dual-energy X-ray absorptiometry for whole body and regional analysis of body composition: validation using piglets and methodologic considerations in infants. Pediatr Res 41, 590–596. [DOI] [PubMed] [Google Scholar]

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