{"title":"一种荧光胆固醇类似物R-Chol可以模拟活细胞中游离胆固醇的动态变化","authors":"Hinako Mogi, Yumi Yamashita, Masumi Sano, Ryo Kadowaki, Takuya Honda, Takafumi Kohama, Hiroyuki Nakamura","doi":"10.1016/j.abb.2025.110600","DOIUrl":null,"url":null,"abstract":"<div><div>Cholesterol is an essential component of the mammalian cell membrane. Elucidating the dynamics of intracellular cholesterol is extremely important for understanding the mechanisms underlying life phenomena and diseases. The fluorescent cholesterol analog, R-Chol, has a fluorescent group at the 3-OH position of free cholesterol, which is less toxic and helpful for studying free cholesterol trafficking in live cells. In the present study, we determined the details of R-Chol dynamics in live cells. R-Chol was taken up by the plasma membrane within 10 min and then incorporated into the cells by endocytosis. Free cholesterol in late endosomes/lysosomes is transported to the endoplasmic reticulum via NPC1 proteins. In <em>Npc1</em>-deficient CHO cells, R-Chol accumulates in late endosomes/lysosomes. R-Chol accumulation in <em>Npc1</em>-deficient cells was attenuated by the overexpression of Rab9, which regulates intracellular transport from late endosomes to the Golgi apparatus. These results indicate that R-Chol incorporated via endocytosis is transported to late endosomes/lysosomes and then to the Golgi apparatus and endoplasmic reticulum by NPC1-dependent and NPC1-independent vesicular trafficking.</div></div>","PeriodicalId":8174,"journal":{"name":"Archives of biochemistry and biophysics","volume":"773 ","pages":"Article 110600"},"PeriodicalIF":3.0000,"publicationDate":"2025-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A fluorescent cholesterol analog, R-Chol, mimics the dynamics of free cholesterol in live cells\",\"authors\":\"Hinako Mogi, Yumi Yamashita, Masumi Sano, Ryo Kadowaki, Takuya Honda, Takafumi Kohama, Hiroyuki Nakamura\",\"doi\":\"10.1016/j.abb.2025.110600\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cholesterol is an essential component of the mammalian cell membrane. Elucidating the dynamics of intracellular cholesterol is extremely important for understanding the mechanisms underlying life phenomena and diseases. The fluorescent cholesterol analog, R-Chol, has a fluorescent group at the 3-OH position of free cholesterol, which is less toxic and helpful for studying free cholesterol trafficking in live cells. In the present study, we determined the details of R-Chol dynamics in live cells. R-Chol was taken up by the plasma membrane within 10 min and then incorporated into the cells by endocytosis. Free cholesterol in late endosomes/lysosomes is transported to the endoplasmic reticulum via NPC1 proteins. In <em>Npc1</em>-deficient CHO cells, R-Chol accumulates in late endosomes/lysosomes. R-Chol accumulation in <em>Npc1</em>-deficient cells was attenuated by the overexpression of Rab9, which regulates intracellular transport from late endosomes to the Golgi apparatus. These results indicate that R-Chol incorporated via endocytosis is transported to late endosomes/lysosomes and then to the Golgi apparatus and endoplasmic reticulum by NPC1-dependent and NPC1-independent vesicular trafficking.</div></div>\",\"PeriodicalId\":8174,\"journal\":{\"name\":\"Archives of biochemistry and biophysics\",\"volume\":\"773 \",\"pages\":\"Article 110600\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-08-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives of biochemistry and biophysics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0003986125003133\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of biochemistry and biophysics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0003986125003133","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
A fluorescent cholesterol analog, R-Chol, mimics the dynamics of free cholesterol in live cells
Cholesterol is an essential component of the mammalian cell membrane. Elucidating the dynamics of intracellular cholesterol is extremely important for understanding the mechanisms underlying life phenomena and diseases. The fluorescent cholesterol analog, R-Chol, has a fluorescent group at the 3-OH position of free cholesterol, which is less toxic and helpful for studying free cholesterol trafficking in live cells. In the present study, we determined the details of R-Chol dynamics in live cells. R-Chol was taken up by the plasma membrane within 10 min and then incorporated into the cells by endocytosis. Free cholesterol in late endosomes/lysosomes is transported to the endoplasmic reticulum via NPC1 proteins. In Npc1-deficient CHO cells, R-Chol accumulates in late endosomes/lysosomes. R-Chol accumulation in Npc1-deficient cells was attenuated by the overexpression of Rab9, which regulates intracellular transport from late endosomes to the Golgi apparatus. These results indicate that R-Chol incorporated via endocytosis is transported to late endosomes/lysosomes and then to the Golgi apparatus and endoplasmic reticulum by NPC1-dependent and NPC1-independent vesicular trafficking.
期刊介绍:
Archives of Biochemistry and Biophysics publishes quality original articles and reviews in the developing areas of biochemistry and biophysics.
Research Areas Include:
• Enzyme and protein structure, function, regulation. Folding, turnover, and post-translational processing
• Biological oxidations, free radical reactions, redox signaling, oxygenases, P450 reactions
• Signal transduction, receptors, membrane transport, intracellular signals. Cellular and integrated metabolism.