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LRP1b shows restricted expression in human tissues and binds to several extracellular ligands, including fibrinogen and apoE – carrying lipoproteins
OBJECTIVE: To investigate low-density lipoprotein receptor-related protein 1b (LRP1b) expression in human tissues and to identify circulating ligands of LRP1b. METHODS AND RESULTS: Using two independent RT-PCR assays, LRP1b mRNA was detected in human brain, thyroid gland, skeletal muscle, and to a l...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3119793/ https://www.ncbi.nlm.nih.gov/pubmed/21420681 http://dx.doi.org/10.1016/j.atherosclerosis.2011.02.030 |
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author | Haas, J. Beer, A.G. Widschwendter, P. Oberdanner, J. Salzmann, K. Sarg, B. Lindner, H. Herz, J. Patsch, J.R. Marschang, P. |
author_facet | Haas, J. Beer, A.G. Widschwendter, P. Oberdanner, J. Salzmann, K. Sarg, B. Lindner, H. Herz, J. Patsch, J.R. Marschang, P. |
author_sort | Haas, J. |
collection | PubMed |
description | OBJECTIVE: To investigate low-density lipoprotein receptor-related protein 1b (LRP1b) expression in human tissues and to identify circulating ligands of LRP1b. METHODS AND RESULTS: Using two independent RT-PCR assays, LRP1b mRNA was detected in human brain, thyroid gland, skeletal muscle, and to a lesser amount in testis but absent in other tissues, including heart, kidney, liver, lung, and placenta. Circulating ligands were purified from human plasma by affinity chromatography using FLAG-tagged recombinant LRP1b ectodomains and identified by mass spectrometry. Using this technique, several potential ligands (fibrinogen, clusterin, vitronectin, histidine rich glycoprotein, serum amyloid P-component, and immunoglobulins) were identified. Direct binding of LRP1b ectodomains to fibrinogen was verified by co-immunoprecipitation. ApoE – carrying lipoproteins were shown to bind to LRP1b ectodomains in a lipoprotein binding assay. Furthermore, binding as well as internalization of very low density lipoproteins by cells expressing an LRP1b minireceptor was demonstrated. DISCUSSION: LRP1b expression in humans appears to be confined to few tissues, which could point out to specialized functions of LRP1b in certain organs. Most of the newly identified LRP1b ligands are well-known factors in blood coagulation and lipoprotein metabolism, suggesting a possible role of LRP1b in atherosclerosis. |
format | Online Article Text |
id | pubmed-3119793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-31197932011-07-19 LRP1b shows restricted expression in human tissues and binds to several extracellular ligands, including fibrinogen and apoE – carrying lipoproteins Haas, J. Beer, A.G. Widschwendter, P. Oberdanner, J. Salzmann, K. Sarg, B. Lindner, H. Herz, J. Patsch, J.R. Marschang, P. Atherosclerosis Article OBJECTIVE: To investigate low-density lipoprotein receptor-related protein 1b (LRP1b) expression in human tissues and to identify circulating ligands of LRP1b. METHODS AND RESULTS: Using two independent RT-PCR assays, LRP1b mRNA was detected in human brain, thyroid gland, skeletal muscle, and to a lesser amount in testis but absent in other tissues, including heart, kidney, liver, lung, and placenta. Circulating ligands were purified from human plasma by affinity chromatography using FLAG-tagged recombinant LRP1b ectodomains and identified by mass spectrometry. Using this technique, several potential ligands (fibrinogen, clusterin, vitronectin, histidine rich glycoprotein, serum amyloid P-component, and immunoglobulins) were identified. Direct binding of LRP1b ectodomains to fibrinogen was verified by co-immunoprecipitation. ApoE – carrying lipoproteins were shown to bind to LRP1b ectodomains in a lipoprotein binding assay. Furthermore, binding as well as internalization of very low density lipoproteins by cells expressing an LRP1b minireceptor was demonstrated. DISCUSSION: LRP1b expression in humans appears to be confined to few tissues, which could point out to specialized functions of LRP1b in certain organs. Most of the newly identified LRP1b ligands are well-known factors in blood coagulation and lipoprotein metabolism, suggesting a possible role of LRP1b in atherosclerosis. Elsevier 2011-06 /pmc/articles/PMC3119793/ /pubmed/21420681 http://dx.doi.org/10.1016/j.atherosclerosis.2011.02.030 Text en © 2011 Elsevier Ireland Ltd. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license |
spellingShingle | Article Haas, J. Beer, A.G. Widschwendter, P. Oberdanner, J. Salzmann, K. Sarg, B. Lindner, H. Herz, J. Patsch, J.R. Marschang, P. LRP1b shows restricted expression in human tissues and binds to several extracellular ligands, including fibrinogen and apoE – carrying lipoproteins |
title | LRP1b shows restricted expression in human tissues and binds to several extracellular ligands, including fibrinogen and apoE – carrying lipoproteins |
title_full | LRP1b shows restricted expression in human tissues and binds to several extracellular ligands, including fibrinogen and apoE – carrying lipoproteins |
title_fullStr | LRP1b shows restricted expression in human tissues and binds to several extracellular ligands, including fibrinogen and apoE – carrying lipoproteins |
title_full_unstemmed | LRP1b shows restricted expression in human tissues and binds to several extracellular ligands, including fibrinogen and apoE – carrying lipoproteins |
title_short | LRP1b shows restricted expression in human tissues and binds to several extracellular ligands, including fibrinogen and apoE – carrying lipoproteins |
title_sort | lrp1b shows restricted expression in human tissues and binds to several extracellular ligands, including fibrinogen and apoe – carrying lipoproteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3119793/ https://www.ncbi.nlm.nih.gov/pubmed/21420681 http://dx.doi.org/10.1016/j.atherosclerosis.2011.02.030 |
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