M. A. Kopanitsa, I. V. Chernykh, A. V. Shchulkin, P. Yu. Mylnikov, A. Yu. Ershov, I. V. Lagoda, A. A. Martynenkov, E. N. Yakusheva
{"title":"金聚糖颗粒对体外糖蛋白功能的影响","authors":"M. A. Kopanitsa, I. V. Chernykh, A. V. Shchulkin, P. Yu. Mylnikov, A. Yu. Ershov, I. V. Lagoda, A. A. Martynenkov, E. N. Yakusheva","doi":"10.1134/S2635167624600482","DOIUrl":null,"url":null,"abstract":"<p>The aim of the work is to evaluate the effect of gold nanoparticles with a surface modified with fucose (Au-Fuc), lactose (Au-Lac), and galactose (Au-Gal) residues on the functional activity and expression of the transporter protein P-glycoprotein (Pgp). The work is performed using Caco-2 and HEK293 cells, which are incubated for 2 and 8 h with solutions of Au-Fuc, Au-Lac, and Au-Gal in a nutrient medium (450 and 300 µg/mL, 700 and 490 µg/mL, and 400 and 250 μg/mL, respectively). The amount of Pgp on the membranes of the Caco-2 cells is determined by the western blot method. The Pgp activity is assessed by the accumulation of fexofenadine Fex (150 µM) in cells by high-performance liquid chromatography (HPLC) with mass detection. Au-Fuc and Au-Gal do not change the amount of Pgp; Au-Lac increases the transporter level by 1.9 and 1.8 times upon 2 and 8 h of incubation respectively. Au-Fuc, Au-Lac, and Au-Gal increase the Pgp content in cells upon 8 h of incubation by 2.6, 3.5, and 5.3 times, which indicates a decrease in Pgp activity. When particles are incubated with HEK293 cells, no increase in the Fex levels are detected, which indicates the absence of a nonspecific increase in membrane permeability. Thus, the tested gold nanoparticles reduce the functional activity of Pgp in vitro.</p>","PeriodicalId":716,"journal":{"name":"Nanotechnologies in Russia","volume":"19 1","pages":"165 - 171"},"PeriodicalIF":0.8000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Influence of Gold Glyconanoparticles on the Functioning of P-Glycoprotein In Vitro\",\"authors\":\"M. A. Kopanitsa, I. V. Chernykh, A. V. Shchulkin, P. Yu. Mylnikov, A. Yu. Ershov, I. V. Lagoda, A. A. Martynenkov, E. N. Yakusheva\",\"doi\":\"10.1134/S2635167624600482\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The aim of the work is to evaluate the effect of gold nanoparticles with a surface modified with fucose (Au-Fuc), lactose (Au-Lac), and galactose (Au-Gal) residues on the functional activity and expression of the transporter protein P-glycoprotein (Pgp). The work is performed using Caco-2 and HEK293 cells, which are incubated for 2 and 8 h with solutions of Au-Fuc, Au-Lac, and Au-Gal in a nutrient medium (450 and 300 µg/mL, 700 and 490 µg/mL, and 400 and 250 μg/mL, respectively). The amount of Pgp on the membranes of the Caco-2 cells is determined by the western blot method. The Pgp activity is assessed by the accumulation of fexofenadine Fex (150 µM) in cells by high-performance liquid chromatography (HPLC) with mass detection. Au-Fuc and Au-Gal do not change the amount of Pgp; Au-Lac increases the transporter level by 1.9 and 1.8 times upon 2 and 8 h of incubation respectively. Au-Fuc, Au-Lac, and Au-Gal increase the Pgp content in cells upon 8 h of incubation by 2.6, 3.5, and 5.3 times, which indicates a decrease in Pgp activity. When particles are incubated with HEK293 cells, no increase in the Fex levels are detected, which indicates the absence of a nonspecific increase in membrane permeability. Thus, the tested gold nanoparticles reduce the functional activity of Pgp in vitro.</p>\",\"PeriodicalId\":716,\"journal\":{\"name\":\"Nanotechnologies in Russia\",\"volume\":\"19 1\",\"pages\":\"165 - 171\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2024-08-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nanotechnologies in Russia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S2635167624600482\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Engineering\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanotechnologies in Russia","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1134/S2635167624600482","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Engineering","Score":null,"Total":0}
Influence of Gold Glyconanoparticles on the Functioning of P-Glycoprotein In Vitro
The aim of the work is to evaluate the effect of gold nanoparticles with a surface modified with fucose (Au-Fuc), lactose (Au-Lac), and galactose (Au-Gal) residues on the functional activity and expression of the transporter protein P-glycoprotein (Pgp). The work is performed using Caco-2 and HEK293 cells, which are incubated for 2 and 8 h with solutions of Au-Fuc, Au-Lac, and Au-Gal in a nutrient medium (450 and 300 µg/mL, 700 and 490 µg/mL, and 400 and 250 μg/mL, respectively). The amount of Pgp on the membranes of the Caco-2 cells is determined by the western blot method. The Pgp activity is assessed by the accumulation of fexofenadine Fex (150 µM) in cells by high-performance liquid chromatography (HPLC) with mass detection. Au-Fuc and Au-Gal do not change the amount of Pgp; Au-Lac increases the transporter level by 1.9 and 1.8 times upon 2 and 8 h of incubation respectively. Au-Fuc, Au-Lac, and Au-Gal increase the Pgp content in cells upon 8 h of incubation by 2.6, 3.5, and 5.3 times, which indicates a decrease in Pgp activity. When particles are incubated with HEK293 cells, no increase in the Fex levels are detected, which indicates the absence of a nonspecific increase in membrane permeability. Thus, the tested gold nanoparticles reduce the functional activity of Pgp in vitro.
期刊介绍:
Nanobiotechnology Reports publishes interdisciplinary research articles on fundamental aspects of the structure and properties of nanoscale objects and nanomaterials, polymeric and bioorganic molecules, and supramolecular and biohybrid complexes, as well as articles that discuss technologies for their preparation and processing, and practical implementation of products, devices, and nature-like systems based on them. The journal publishes original articles and reviews that meet the highest scientific quality standards in the following areas of science and technology studies: self-organizing structures and nanoassemblies; nanostructures, including nanotubes; functional and structural nanomaterials; polymeric, bioorganic, and hybrid nanomaterials; devices and products based on nanomaterials and nanotechnology; nanobiology and genetics, and omics technologies; nanobiomedicine and nanopharmaceutics; nanoelectronics and neuromorphic computing systems; neurocognitive systems and technologies; nanophotonics; natural science methods in a study of cultural heritage items; metrology, standardization, and monitoring in nanotechnology.