Open AccessSmall molecule inhibitors provide insights into the relevance of LAT1 and LAT2 in materno‐foetal amino acid transport
Author(s) -
Zaugg Jonas,
Huang Xiao,
Ziegler Fabian,
Rubin Matthias,
Graff Julien,
Müller Jennifer,
MoserHässig Ruedi,
Powell Theresa,
Gertsch Jürg,
Altmann KarlHeinz,
Albrecht Christiane
Publication year - 2020
Publication title -
journal of cellular and molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.44
H-Index - 130
eISSN - 1582-4934
pISSN - 1582-1838
DOI - 10.1111/jcmm.15840
Subject(s) - syncytiotrophoblast , leucine , transporter , amino acid transporter , fetal membrane , amino acid , biochemistry , biology , placenta , efflux , trophoblast , chemistry , fetus , gene , pregnancy , genetics
Abstract The placenta supplies the foetus with critical nutrients such as essential amino acids (AA, eg leucine) for development and growth. It also represents a cellular barrier which is formed by a polarized, differentiated syncytiotrophoblast (STB) monolayer. Active Na + ‐independent leucine transport across the placenta is mainly attributed to the System L transporters LAT1/SLC7A5 and LAT2/SLC7A8. This study explored the influence of trophoblast differentiation on the activity of LAT1/LAT2 and the relevance of LAT1/LAT2 in leucine uptake and transfer in trophoblasts by applying specific small molecule inhibitors (JPH203/JG336/JX009). L‐leucine uptake (total dose = 167 μmol/L) was sensitive to LAT1‐specific inhibition by JPH203 (EC 50 = 2.55 µmol/L). The inhibition efficiency of JPH203 was increased by an additional methoxy group in the JPH203‐derivate JG336 (EC 50 = 1.99 µmol/L). Interestingly, JX009 showed efficient System L inhibition (EC 50 = 2.35 µmol/L) and was the most potent inhibitor of leucine uptake in trophoblasts. The application of JPH203 and JX009 in Transwell ® ‐based leucine transfer revealed LAT1 as the major accumulative transporter at the apical membrane, but other System L transporters such as LAT2 as rate‐limiting for leucine efflux across the basal membrane. Therefore, differential specificity of the applied inhibitors allowed for estimation of the contribution of LAT1 and LAT2 in materno‐foetal AA transfer and their potential impact in pregnancy diseases associated with impaired foetal growth.