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Profiling of kidney vascular endothelial cell plasma membrane proteins by liquid chromatography–tandem mass spectrometry
BACKGROUND: Vascular endothelial cells (VECs) play crucial roles in physiological and pathologic conditions in tissues and organs. Most of these roles are related to VEC plasma membrane proteins. In the kidney, VECs are closely associated with structures and functions; however, plasma membrane prote...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684716/ https://www.ncbi.nlm.nih.gov/pubmed/23229650 http://dx.doi.org/10.1007/s10157-012-0708-1 |
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author | Liu, Zan Xu, Bo Nameta, Masaaki Zhang, Ying Magdeldin, Sameh Yoshida, Yutaka Yamamoto, Keiko Fujinaka, Hidehiko Yaoita, Eishin Tasaki, Masayuki Nakagawa, Yuki Saito, Kazuhide Takahashi, Kota Yamamoto, Tadashi |
author_facet | Liu, Zan Xu, Bo Nameta, Masaaki Zhang, Ying Magdeldin, Sameh Yoshida, Yutaka Yamamoto, Keiko Fujinaka, Hidehiko Yaoita, Eishin Tasaki, Masayuki Nakagawa, Yuki Saito, Kazuhide Takahashi, Kota Yamamoto, Tadashi |
author_sort | Liu, Zan |
collection | PubMed |
description | BACKGROUND: Vascular endothelial cells (VECs) play crucial roles in physiological and pathologic conditions in tissues and organs. Most of these roles are related to VEC plasma membrane proteins. In the kidney, VECs are closely associated with structures and functions; however, plasma membrane proteins in kidney VECs remain to be fully elucidated. METHODS: Rat kidneys were perfused with cationic colloidal silica nanoparticles (CCSN) to label the VEC plasma membrane. The CCSN-labeled plasma membrane fraction was collected by gradient ultracentrifugation. The VEC plasma membrane or whole-kidney lysate proteins were separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis and digested with trypsin in gels for liquid chromatography–tandem mass spectrometry. Enrichment analysis was then performed. RESULTS: The VEC plasma membrane proteins were purified by the CCSN method with high yield (approximately 20 μg from 1 g of rat kidney). By Mascot search, 582 proteins were identified in the VEC plasma membrane fraction, and 1,205 proteins were identified in the kidney lysate. In addition to 16 VEC marker proteins such as integrin beta-1 and intercellular adhesion molecule-2 (ICAM-2), 8 novel proteins such as Deltex 3-like protein and phosphatidylinositol binding clathrin assembly protein (PICALM) were identified. As expected, many key functions of plasma membranes in general and of endothelial cells in particular (i.e., leukocyte adhesion) were significantly overrepresented in the proteome of CCSN-labeled kidney VEC fraction. CONCLUSIONS: The CCSN method is a reliable technique for isolation of VEC plasma membrane from the kidney, and proteomic analysis followed by bioinformatics revealed the characteristics of in vivo VECs in the kidney. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10157-012-0708-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3684716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-36847162013-06-20 Profiling of kidney vascular endothelial cell plasma membrane proteins by liquid chromatography–tandem mass spectrometry Liu, Zan Xu, Bo Nameta, Masaaki Zhang, Ying Magdeldin, Sameh Yoshida, Yutaka Yamamoto, Keiko Fujinaka, Hidehiko Yaoita, Eishin Tasaki, Masayuki Nakagawa, Yuki Saito, Kazuhide Takahashi, Kota Yamamoto, Tadashi Clin Exp Nephrol Original Article BACKGROUND: Vascular endothelial cells (VECs) play crucial roles in physiological and pathologic conditions in tissues and organs. Most of these roles are related to VEC plasma membrane proteins. In the kidney, VECs are closely associated with structures and functions; however, plasma membrane proteins in kidney VECs remain to be fully elucidated. METHODS: Rat kidneys were perfused with cationic colloidal silica nanoparticles (CCSN) to label the VEC plasma membrane. The CCSN-labeled plasma membrane fraction was collected by gradient ultracentrifugation. The VEC plasma membrane or whole-kidney lysate proteins were separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis and digested with trypsin in gels for liquid chromatography–tandem mass spectrometry. Enrichment analysis was then performed. RESULTS: The VEC plasma membrane proteins were purified by the CCSN method with high yield (approximately 20 μg from 1 g of rat kidney). By Mascot search, 582 proteins were identified in the VEC plasma membrane fraction, and 1,205 proteins were identified in the kidney lysate. In addition to 16 VEC marker proteins such as integrin beta-1 and intercellular adhesion molecule-2 (ICAM-2), 8 novel proteins such as Deltex 3-like protein and phosphatidylinositol binding clathrin assembly protein (PICALM) were identified. As expected, many key functions of plasma membranes in general and of endothelial cells in particular (i.e., leukocyte adhesion) were significantly overrepresented in the proteome of CCSN-labeled kidney VEC fraction. CONCLUSIONS: The CCSN method is a reliable technique for isolation of VEC plasma membrane from the kidney, and proteomic analysis followed by bioinformatics revealed the characteristics of in vivo VECs in the kidney. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10157-012-0708-1) contains supplementary material, which is available to authorized users. Springer Japan 2012-12-11 2013 /pmc/articles/PMC3684716/ /pubmed/23229650 http://dx.doi.org/10.1007/s10157-012-0708-1 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Liu, Zan Xu, Bo Nameta, Masaaki Zhang, Ying Magdeldin, Sameh Yoshida, Yutaka Yamamoto, Keiko Fujinaka, Hidehiko Yaoita, Eishin Tasaki, Masayuki Nakagawa, Yuki Saito, Kazuhide Takahashi, Kota Yamamoto, Tadashi Profiling of kidney vascular endothelial cell plasma membrane proteins by liquid chromatography–tandem mass spectrometry |
title | Profiling of kidney vascular endothelial cell plasma membrane proteins by liquid chromatography–tandem mass spectrometry |
title_full | Profiling of kidney vascular endothelial cell plasma membrane proteins by liquid chromatography–tandem mass spectrometry |
title_fullStr | Profiling of kidney vascular endothelial cell plasma membrane proteins by liquid chromatography–tandem mass spectrometry |
title_full_unstemmed | Profiling of kidney vascular endothelial cell plasma membrane proteins by liquid chromatography–tandem mass spectrometry |
title_short | Profiling of kidney vascular endothelial cell plasma membrane proteins by liquid chromatography–tandem mass spectrometry |
title_sort | profiling of kidney vascular endothelial cell plasma membrane proteins by liquid chromatography–tandem mass spectrometry |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684716/ https://www.ncbi.nlm.nih.gov/pubmed/23229650 http://dx.doi.org/10.1007/s10157-012-0708-1 |
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