دورية أكاديمية
Transport of LDL-derived Cholesterol from the NPC1 Compartment to the ER Involves the Trans-Golgi Network and the SNARE Protein Complex
| العنوان: | Transport of LDL-derived Cholesterol from the NPC1 Compartment to the ER Involves the Trans-Golgi Network and the SNARE Protein Complex |
|---|---|
| المؤلفون: | Urano, Yasuomi, Watanabe, Hiroshi, Murphy, Stephanie R, Shibuya, Yohei, Geng, Yong, Peden, Andrew, Chang, Catherine, Chang, Ta Yuan |
| المصدر: | Dartmouth Scholarship |
| بيانات النشر: | Dartmouth Digital Commons |
| سنة النشر: | 2008 |
| المجموعة: | Dartmouth Digital Commons (Dartmouth College) |
| مصطلحات موضوعية: | adenosine triphosphate, animals, cho cells, cell fractionation, cholesterol, ldl, metabolism, cricetinae, cricetulus, endoplasmic reticulum, endosomes, membrane proteins, analysis, protein transport, rna, small interfering, pharmacology, snare proteins, genetics, tritium, trans-golgi network, Medical Biochemistry, Medical Cell Biology, Medical Sciences, Medicine and Health Sciences |
| الوصف: | Mammalian cells acquire cholesterol mainly from LDL. LDL enter the endosomes, allowing cholesteryl esters to be hydrolyzed by acid lipase. The hydrolyzed cholesterol (LDL-CHOL) enters the Niemann-Pick type C1 (NPC1)-containing endosomal compartment en route to various destinations. Whether the Golgi is involved in LDL-CHOL transport downstream of the NPC1 compartment has not been demonstrated. Using subcellular fractionation and immunoadsorption to enrich for specific membrane fractions, here we show that, when parental Chinese hamster ovary (CHO) cells are briefly exposed to (3)H-cholesteryl linoleate (CL) labeled-LDL, newly liberated (3)H-LDL-CHOL appears in membranes rich in trans-Golgi network (TGN) long before it becomes available for re-esterification at the endoplasmic reticulum (ER) or for efflux at the plasma membrane. In mutant cells lacking NPC1, the appearance of newly liberated (3)H-LDL-CHOL in the TGN-rich fractions is much reduced. We next report a reconstituted transport system that recapitulates the transport of LDL-CHOL to the TGN and to the ER. The transport system requires ATP and cytosolic factors and depends on functionality of NPC1. We demonstrate that knockdown by RNAi of 3 TGN-specific SNAREs (VAMP4, syntaxin 6, and syntaxin 16) reduces >/=50% of the LDL-CHOL transport in intact cells and in vitro. These results show that vesicular trafficking is involved in transporting a significant portion of LDL-CHOL from the NPC1-containing endosomal compartment to the TGN before its arrival at the ER. |
| نوع الوثيقة: | text |
| وصف الملف: | application/pdf |
| اللغة: | unknown |
| العلاقة: | https://digitalcommons.dartmouth.edu/facoa/1182Test; https://digitalcommons.dartmouth.edu/context/facoa/article/2185/viewcontent/PMC2575451.pdfTest |
| DOI: | 10.1073/pnas.0807450105 |
| الإتاحة: | https://doi.org/10.1073/pnas.0807450105Test https://digitalcommons.dartmouth.edu/facoa/1182Test https://digitalcommons.dartmouth.edu/context/facoa/article/2185/viewcontent/PMC2575451.pdfTest |
| رقم الانضمام: | edsbas.69B60DA5 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1073/pnas.0807450105 |
|---|