Objective:
To investigate the possible role of human placenta in providing D-serine to the developing fetus.
Methods:
Expression of serine racemase in placenta was determined by reverse transcriptase polymerase chain reaction and northern analysis and confirmed by subsequent cloning. The transport of D-serine by human ATB0 was characterized by expressing the cloned cDNA transiently in mammalian cells using the vaccinia virus expression system. D-serine levels in maternal and fetal blood were measured by fluorescence high-performance liquid chromatography (HPLC) after derivatization of the amino adids with o-phthaldialdehyde and N-tertiary-butyloxycarbonyl-L-cysteine.
Results:
mRNA for serine racemase was detected in placenta. ATB0 was capable of D-serine transport, and the transport process is obligatorily dependent on sodium (Na+) with a Na+: substrate stoichiometry of 1:1 and saturable with a Michaelis-Menten constant of 310 ± 30 μM. Furthermore, studies have shown and ATB0 is not expressed in the maternal-facing brush border membrane of human placental syncytiotrophoblast. The circulating concentration of D-serine in maternal serum is 5.8 ± 0.5 μM, and the corresponding value in the fetal serum is 14.6 ± 1.2 μM, indicating a two- to three-fold higher concentration of D-serine in the fetus than in the mother.
Conclusion:
We speculate that D-serine is synthesized in human placenta by the recemization of L-serine and that ATB0, expressed on the basal membrane of the syncytiotrophoblast, mediates the efflux of D-serine into fetal circulation in exchange for other amino acids in fetal blood.