期刊
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
卷 474, 期 12, 页码 1249-1262出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00424-022-02752-1
关键词
Glycine; Hyperosmotic conditions; PC-3 cells; Sarcosine; SNAT2; Solute carrier
类别
资金
- Carlsberg foundation
Solute carriers (SLC) play a crucial role in the uptake of sarcosine and glycine in prostate cancer cells, and hyperosmotic stress can affect their uptake.
Solute carriers (SLC) are important membrane transport proteins in normal and pathophysiological cells. The aim was to identify amino acid SLC(s) responsible for uptake of sarcosine and glycine in prostate cancer cells and investigate the impact hereon of hyperosmotic stress. Uptake of C-14-sarcosine and H-3-glycine was measured in human prostate cancer (PC-3) cells cultured under isosmotic (300 mOsm/kg) and hyperosmotic (500 mOsm/kg) conditions for 24 h. Hyperosmotic culture medium was obtained by supplementing the medium with 200 mM of the trisaccharide raffinose. Amino acid SLC expression was studied using RT-PCR, real-time PCR, and western blotting. siRNA knockdown of SNAT2 was performed. Experiments were conducted in at least 3 independent cell passages. The uptake of Sar and Gly was increased approximately 8-ninefold in PC-3 cells after 24 h hyperosmotic culture. PAT1 mRNA and protein could not be detected, while SNAT2 was upregulated at the mRNA and protein level. Transfection with SNAT2-specific siRNA reduced V-max of Sar uptake from 2653 +/- 38 to 513 +/- 38 nmol mg protein(-1) min(-1), without altering the K-m value (3.19 +/- 0.13 vs. 3.42 +/- 0.71 mM), indicating that SNAT2 is responsible for at least 80% of Sar uptake in hyperosmotic cultured PC-3 cells. SNAT2 is upregulated in hyperosmotic stressed prostate cancer cells and SNAT2 is responsible for cellular sarcosine and glycine uptake in hyperosmotic cultured PC-3 cells. Sar is identified as a substrate for SNAT2, and this has physiological implications for understanding cellular solute transport in prostate cancer cells.
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