Structure, Function, and Tissue Expression Pattern of Human SN2, a Subtype of the Amino Acid Transport System N

2001 ◽  
Vol 281 (5) ◽  
pp. 1343-1348 ◽  
Author(s):  
Takeo Nakanishi ◽  
Mitsuru Sugawara ◽  
Wei Huang ◽  
Robert G. Martindale ◽  
Frederick H. Leibach ◽  
...  
Keyword(s):  
Amino Acid ◽  
Structure Function ◽  
Expression Pattern ◽  
Transport System ◽  
Amino Acid Transport ◽  
Tissue Expression ◽  
Acid Transport ◽  
Tissue Expression Pattern ◽  
Amino Acid Transport System

Osmotic Regulation of ATA2 mRNA Expression and Amino Acid Transport System A Activity

2001 ◽  
Vol 283 (1) ◽  
pp. 174-178 ◽  
Author(s):  
Roberta R. Alfieri ◽  
Pier-Giorgio Petronini ◽  
Mara A. Bonelli ◽  
Alessandro E. Caccamo ◽  
Andrea Cavazzoni ◽  
...  
Keyword(s):  
Amino Acid ◽  
Mrna Expression ◽  
Transport System ◽  
Amino Acid Transport ◽  
Osmotic Regulation ◽  
Acid Transport ◽  
Amino Acid Transport System ◽  
System A

Expression and regulation of 4F2hc and hLAT1 in human trophoblasts

2002 ◽  
Vol 282 (1) ◽  
pp. C196-C204 ◽  
Author(s):  
Yoko Okamoto ◽  
Masahiro Sakata ◽  
Kazuhiro Ogura ◽  
Toshiya Yamamoto ◽  
Masaaki Yamaguchi ◽  
...  
Keyword(s):  
Amino Acid ◽  
Cell Line ◽  
Transport System ◽  
Human Placenta ◽  
Amino Acid Transport ◽  
Calcium Ionophore ◽  
Acid Transport ◽  
Amino Acid Transport System ◽  
System L ◽  
Choriocarcinoma Cell Line

The neutral amino acid transport system L is a sodium-independent transport system in human placenta and choriocarcinoma cells. Recently, it was found that the heterodimer composed of hLAT1 (a light-chain protein) and 4F2 heavy chain (4F2hc), a type II transmembrane glycoprotein, is responsible for system L amino acid transport. We found that the mRNAs of 4F2hc and hLAT1 were expressed in the human placenta and a human choriocarcinoma cell line. The levels of the 4F2hc and hLAT1 proteins in the human placenta increased at full term compared with those at midtrimester. Immunohistochemical data showed that these proteins were localized mainly in the placental apical membrane. Data from leucine uptake experiments, Northern blot analysis, and immunoblot analysis showed that this transport system was partially regulated by protein kinase C and calcium ionophore in the human choriocarcinoma cell line. Our results suggest that the heterodimer of 4F2hc and hLAT1 may play an important role in placental amino acid transport system L.

Cloning and functional characterization of a new subtype of the amino acid transport system N

2001 ◽  
Vol 281 (6) ◽  
pp. C1757-C1768 ◽  
Author(s):  
Takeo Nakanishi ◽  
Ramesh Kekuda ◽  
You-Jun Fei ◽  
Takahiro Hatanaka ◽  
Mitsuru Sugawara ◽  
...  
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Transport System ◽  
Amino Acid Transport ◽  
Mammalian Cells ◽  
Functional Characterization ◽  
Isobutyric Acid ◽  
Xenopus Laevis Oocytes ◽  
Acid Transport ◽  
Amino Acid Transport System

We have cloned a new subtype of the amino acid transport system N2 (SN2 or second subtype of system N) from rat brain. Rat SN2 consists of 471 amino acids and belongs to the recently identified glutamine transporter gene family that consists of system N and system A. Rat SN2 exhibits 63% identity with rat SN1. It also shows considerable sequence identity (50–56%) with the members of the amino acid transporter A subfamily. In the rat, SN2 mRNA is most abundant in the liver but is detectable in the brain, lung, stomach, kidney, testis, and spleen. When expressed in Xenopus laevis oocytes and in mammalian cells, rat SN2 mediates Na+-dependent transport of several neutral amino acids, including glycine, asparagine, alanine, serine, glutamine, and histidine. The transport process is electrogenic, Li+tolerant, and pH sensitive. The transport mechanism involves the influx of Na+ and amino acids coupled to the efflux of H+, resulting in intracellular alkalization. Proline, α-(methylamino)isobutyric acid, and anionic and cationic amino acids are not recognized by rat SN2.

scholarly journals The EGF Receptor Promotes the Malignant Potential of Glioma by Regulating Amino Acid Transport System xc(—)

2016 ◽  
Vol 76 (10) ◽  
pp. 2954-2963 ◽  
Author(s):  
Kenji Tsuchihashi ◽  
Shogo Okazaki ◽  
Mitsuyo Ohmura ◽  
Miyuki Ishikawa ◽  
Oltea Sampetrean ◽  
...  
Keyword(s):  
Amino Acid ◽  
Transport System ◽  
Amino Acid Transport ◽  
Egf Receptor ◽  
Malignant Potential ◽  
Acid Transport ◽  
Amino Acid Transport System

scholarly journals Expression and adaptive regulation of amino acid transport system A in a placental cell line under amino acid restriction

Reproduction ◽  
2006 ◽  
Vol 131 (5) ◽  
pp. 951-960 ◽  
Author(s):  
H N Jones ◽  
C J Ashworth ◽  
K R Page ◽  
H J McArdle
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Cell Line ◽  
Transport System ◽  
Amino Acid Transport ◽  
Essential Amino Acids ◽  
Acid Transport ◽  
Amino Acid Transport System ◽  
Transcellular Transport ◽  
System A

Trans-placental transport of amino acids is vital for the developing fetus. Using the BeWo cell line as a placental model, we investigated the effect of restricting amino acid availability on amino acid transport system type A. BeWo cells were cultured either in amino acid-depleted (without non-essential amino acids) or control media for 1, 3, 5 or 6 h. System A function was analysed using α(methyl-amino)isobutyric acid (MeAIB) transcellular transport studies. Transporter (sodium coupled neutral amino acid transporter (SNAT1/2)) expression was analysed at mRNA and protein level by Northern and Western blotting respectively. Localisation was carried out using immunocytochemistry. MeAIB transcellular transport was significantly (P< 0.05) increased by incubation of the cells in amino acid-depleted medium for 1 h, and longer incubation times caused further increases in the rate of transfer. However, the initial response was not accompanied by an increase in SNAT2 mRNA; this occurred only after 3 h and further increased for the rest of the 6-h incubation. Similarly, it took several hours for a significant increase in SNAT2 protein expression. In contrast, relocalisation of existing SNAT2 transporters occurred within 30 min of amino acid restriction and continued throughout the 6-h incubation. When the cells were incubated in medium with even lower amino acid levels (without non-essential plus 0.5 × essential amino acids), SNAT2 mRNA levels showed further significant (P< 0.0001) up-regulation. However, incubation of cells in depleted medium for 6 h caused a significant (P= 0.014) decrease in the expression of SNAT1 mRNA. System L type amino acid transporter 2 (LAT2) expression was not changed by amino acid restriction, indicating that the responses seen in the system A transporters were not a general cell response. These data have shown that placental cells adaptin vitroto nutritional stress and have identified the physiological, biochemical and genomic mechanisms involved.

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