Relative contribution of different l-arginine sources to the substrate supply of endothelial nitric oxide synthase

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• 作者：Susanne Karbach¹ ;   ; ² ;   ; ^a ; Alexandra Simon² ;   ; ^a ; Anita Slenzka^a ; Isabel Jaenecke^a ; Alice Habermeier^a ; Ursula Martiné ; ^a ; Ulrich Fö ; rstermann^a ; Ellen I. Closs ;   ; ^a ;   ; ^{Closs@uni-mainz.de}
• 关键词：Endothelial NO synthase (eNOS) ; Endothelial dysfunction ; Citrulline to arginine recycling ; Lysosomal and proteasomal protein degradation ; Peptide histidine transporter (PHT1)
• 刊名：Journal of Molecular and Cellular Cardiology
• 出版年：2011
• 出版时间：November 2011
• 年：2011
• 卷：51
• 期：5
• 页码：855-861
• 全文大小：1377 K

文摘

In certain cases of endothelial dysfunction l-arginine becomes rate-limiting for NO synthesis in spite of sufficiently high plasma concentrations of the amino acid. To better understand this phenomenon, we investigated routes of substrate supply to endothelial nitric oxide synthase (eNOS). Our previous data with human umbilical vein (HUVEC) and EA.hy.926 endothelial cells demonstrated that eNOS can obtain its substrate from the conversion of l-citrulline to l-arginine and from protein breakdown. In the present study, we determined the quantitative contribution of proteasomal and lysosomal protein degradation and investigated to what extent extracellular peptides and l-citrulline can provide substrate to eNOS. The RFL-6 reporter cell assay was used to measure eNOS activity in human EA.hy926 endothelial cells. Individual proteasome and lysosome inhibition reduced eNOS activity in EA.hy926 cells only slightly. However, the combined inhibition had a pronounced reducing effect. eNOS activity was fully restored by supplementing either l-citrulline or l-arginine-containing dipeptides. Histidine prevented the restoration of eNOS activity by the dipeptide, suggesting that a transporter accepting both, peptides and histidine, mediates the uptake of the extracellular peptide. In fact, the peptide and histidine transporter PHT1 was expressed in EA.hy926 cells and HUVECs (qRT/PCR). Our study thus demonstrates that l-citrulline and l-arginine-containing peptides derived from either intracellular protein breakdown or from the extracellular space seem to be good substrate sources for eNOS.