Engineered red blood cells carrying PCSK9 inhibitors persistently lower LDL and prevent obesity.

Low plasma levels of Proprotein Convertase Subtilisin/Kexin 9 (PCSK9) are associated with decreased low-density lipoprotein (LDL) cholesterol and a reduced risk of cardiovascular disease. PCSK9 binds to the epidermal growth factor-like repeat A (EGFA) domain of LDL receptors (LDLR), very low-density...

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Autores principales: Rhogerry Deshycka, Valentino Sudaryo, Nai-Jia Huang, Yushu Xie, Liyan Y Smeding, Moon Kyung Choi, Hidde L Ploegh, Harvey F Lodish, Novalia Pishesha
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:578e74400dc64fdb8e36d78c1909d0172021-12-02T20:04:26ZEngineered red blood cells carrying PCSK9 inhibitors persistently lower LDL and prevent obesity.1932-620310.1371/journal.pone.0259353https://doaj.org/article/578e74400dc64fdb8e36d78c1909d0172021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0259353https://doaj.org/toc/1932-6203Low plasma levels of Proprotein Convertase Subtilisin/Kexin 9 (PCSK9) are associated with decreased low-density lipoprotein (LDL) cholesterol and a reduced risk of cardiovascular disease. PCSK9 binds to the epidermal growth factor-like repeat A (EGFA) domain of LDL receptors (LDLR), very low-density lipoprotein receptors (VLDLR), apolipoprotein E receptor 2 (ApoER2), and lipoprotein receptor-related protein 1 (LRP1) and accelerates their degradation, thus acting as a key regulator of lipid metabolism. Antibody and RNAi-based PCSK9 inhibitor treatments lower cholesterol and prevent cardiovascular incidents in patients, but their high-cost hampers market penetration. We sought to develop a safe, long-term and one-time solution to treat hyperlipidemia. We created a cDNA encoding a chimeric protein in which the extracellular N- terminus of red blood cells (RBCs) specific glycophorin A was fused to the LDLR EGFA domain and introduced this gene into mouse bone marrow hematopoietic stem and progenitor cells (HSPCs). Following transplantation into irradiated mice, the animals produced RBCs with the EGFA domain (EGFA-GPA RBCs) displayed on their surface. These animals showed significantly reduced plasma PCSK9 (66.5% decrease) and reduced LDL levels (40% decrease) for as long as 12 months post-transplantation. Furthermore, the EGFA- GPA mice remained lean for life and maintained normal body weight under a high-fat diet. Hematopoietic stem cell gene therapy can generate red blood cells expressing an EGFA-glycophorin A chimeric protein as a practical and long-term strategy for treating chronic hyperlipidemia and obesity.Rhogerry DeshyckaValentino SudaryoNai-Jia HuangYushu XieLiyan Y SmedingMoon Kyung ChoiHidde L PloeghHarvey F LodishNovalia PisheshaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 11, p e0259353 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Rhogerry Deshycka
Valentino Sudaryo
Nai-Jia Huang
Yushu Xie
Liyan Y Smeding
Moon Kyung Choi
Hidde L Ploegh
Harvey F Lodish
Novalia Pishesha
Engineered red blood cells carrying PCSK9 inhibitors persistently lower LDL and prevent obesity.
description Low plasma levels of Proprotein Convertase Subtilisin/Kexin 9 (PCSK9) are associated with decreased low-density lipoprotein (LDL) cholesterol and a reduced risk of cardiovascular disease. PCSK9 binds to the epidermal growth factor-like repeat A (EGFA) domain of LDL receptors (LDLR), very low-density lipoprotein receptors (VLDLR), apolipoprotein E receptor 2 (ApoER2), and lipoprotein receptor-related protein 1 (LRP1) and accelerates their degradation, thus acting as a key regulator of lipid metabolism. Antibody and RNAi-based PCSK9 inhibitor treatments lower cholesterol and prevent cardiovascular incidents in patients, but their high-cost hampers market penetration. We sought to develop a safe, long-term and one-time solution to treat hyperlipidemia. We created a cDNA encoding a chimeric protein in which the extracellular N- terminus of red blood cells (RBCs) specific glycophorin A was fused to the LDLR EGFA domain and introduced this gene into mouse bone marrow hematopoietic stem and progenitor cells (HSPCs). Following transplantation into irradiated mice, the animals produced RBCs with the EGFA domain (EGFA-GPA RBCs) displayed on their surface. These animals showed significantly reduced plasma PCSK9 (66.5% decrease) and reduced LDL levels (40% decrease) for as long as 12 months post-transplantation. Furthermore, the EGFA- GPA mice remained lean for life and maintained normal body weight under a high-fat diet. Hematopoietic stem cell gene therapy can generate red blood cells expressing an EGFA-glycophorin A chimeric protein as a practical and long-term strategy for treating chronic hyperlipidemia and obesity.
format article
author Rhogerry Deshycka
Valentino Sudaryo
Nai-Jia Huang
Yushu Xie
Liyan Y Smeding
Moon Kyung Choi
Hidde L Ploegh
Harvey F Lodish
Novalia Pishesha
author_facet Rhogerry Deshycka
Valentino Sudaryo
Nai-Jia Huang
Yushu Xie
Liyan Y Smeding
Moon Kyung Choi
Hidde L Ploegh
Harvey F Lodish
Novalia Pishesha
author_sort Rhogerry Deshycka
title Engineered red blood cells carrying PCSK9 inhibitors persistently lower LDL and prevent obesity.
title_short Engineered red blood cells carrying PCSK9 inhibitors persistently lower LDL and prevent obesity.
title_full Engineered red blood cells carrying PCSK9 inhibitors persistently lower LDL and prevent obesity.
title_fullStr Engineered red blood cells carrying PCSK9 inhibitors persistently lower LDL and prevent obesity.
title_full_unstemmed Engineered red blood cells carrying PCSK9 inhibitors persistently lower LDL and prevent obesity.
title_sort engineered red blood cells carrying pcsk9 inhibitors persistently lower ldl and prevent obesity.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/578e74400dc64fdb8e36d78c1909d017
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