Characterization of amino acid transport system L in HTB-41 human salivary gland epidermoid carcinoma cells.

Abstract

BACKGROUND:

The amino acid transport system L is a major nutrient transport system that is responsible for transport of neutral amino acids, including several essential amino acids. The current study attempted to investigate the expression and functional characterization of amino acid transport system L in HTB-41 human submaxillary salivary gland epidermoid carcinoma cells.

MATERIALS AND METHODS:

RT-PCR analysis, Western blot analysis and amino acid transport measurements were used.

RESULTS:

The HTB-41 cells expressed the L-type amino acid transporter 1 (LAT1) together with its associating protein heavy chain of 4F2 antigen (4F2hc) in the plasma membrane, whereas the HTB-41 cells did not express the L-type amino acid transporter 2 (LAT2). The uptakes of [14C]L-leucine were Na+-independent and completely inhibited by a system L selective inhibitor, 2-aminobicyclo-(2,2,1)-heptane-2-carboxylic acid (BCH). The affinity of [14C]L-leucine uptake and the inhibition profile of [14C]L-leucine uptake by various L-amino acids in the HTB-41 cells were comparable with those for the LAT1 expressed in Xenopus oocytes.

CONCLUSION:

The transport of neutral amino acids including several essential amino acids into the HTB-41 human submaxillary salivary gland epidermoid carcinoma cells are mediated by LAT1.

• Authors: No-Seung Park, Su-Gwan Kim, Hak-Kyun Kim, Seong-Yong Moon, Chun Sung Kim, Seon-Ho Cho, Yoshikatsu Kanai, Hitoshi Endou, Do Kyung Kim
• Journal: Anticancer research (Anticancer Res) 2008 Sep-Oct Vol. 28 Issue 5A Pg. 2649-55 ISSN: 0250-7005 [Print] Greece
• PMID: 19035290 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Amino Acid Transport System L
• Amino Acids, Cyclic
• Carbon Radioisotopes
• 2-aminobicyclo(2,2,1)heptane-2-carboxylic acid
• Leucine

Topics

• Amino Acid Transport System L (antagonists & inhibitors, metabolism)
• Amino Acids, Cyclic (pharmacology)
• Blotting, Western
• Carbon Radioisotopes
• Carcinoma, Squamous Cell (metabolism)
• Cell Line, Tumor
• Humans
• Leucine (metabolism, pharmacokinetics)
• Reverse Transcriptase Polymerase Chain Reaction
• Salivary Gland Neoplasms (metabolism)
• Submandibular Gland (metabolism, pathology)