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Golgi-endosome transport mediated by M6PR facilitates release of antisense oligonucleotides from endosomes
Release of phosphorothioate antisense oligonucleotides (PS-ASOs) from late endosomes (LEs) is a rate-limiting step and a poorly defined process for productive intracellular ASO drug delivery. Here, we examined the role of Golgi-endosome transport, specifically M6PR shuttling mediated by GCC2, in PS-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026651/ https://www.ncbi.nlm.nih.gov/pubmed/31840180 http://dx.doi.org/10.1093/nar/gkz1171 |
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author | Liang, Xue-hai Sun, Hong Hsu, Chih-Wei Nichols, Joshua G Vickers, Timothy A De Hoyos, Cheryl L Crooke, Stanley T |
author_facet | Liang, Xue-hai Sun, Hong Hsu, Chih-Wei Nichols, Joshua G Vickers, Timothy A De Hoyos, Cheryl L Crooke, Stanley T |
author_sort | Liang, Xue-hai |
collection | PubMed |
description | Release of phosphorothioate antisense oligonucleotides (PS-ASOs) from late endosomes (LEs) is a rate-limiting step and a poorly defined process for productive intracellular ASO drug delivery. Here, we examined the role of Golgi-endosome transport, specifically M6PR shuttling mediated by GCC2, in PS-ASO trafficking and activity. We found that reduction in cellular levels of GCC2 or M6PR impaired PS-ASO release from endosomes and decreased PS-ASO activity in human cells. GCC2 relocated to LEs upon PS-ASO treatment, and M6PR also co-localized with PS-ASOs in LEs or on LE membranes. These proteins act through the same pathway to influence PS-ASO activity, with GCC2 action preceding that of M6PR. Our data indicate that M6PR binds PS-ASOs and facilitates their vesicular escape. The co-localization of M6PR and of GCC2 with ASOs is influenced by the PS modifications, which have been shown to enhance the affinity of ASOs for proteins, suggesting that localization of these proteins to LEs is mediated by ASO-protein interactions. Reduction of M6PR levels also decreased PS-ASO activity in mouse cells and in livers of mice treated subcutaneously with PS-ASO, indicating a conserved mechanism. Together, these results demonstrate that the transport machinery between LE and Golgi facilitates PS-ASO release. |
format | Online Article Text |
id | pubmed-7026651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70266512020-02-25 Golgi-endosome transport mediated by M6PR facilitates release of antisense oligonucleotides from endosomes Liang, Xue-hai Sun, Hong Hsu, Chih-Wei Nichols, Joshua G Vickers, Timothy A De Hoyos, Cheryl L Crooke, Stanley T Nucleic Acids Res Molecular Biology Release of phosphorothioate antisense oligonucleotides (PS-ASOs) from late endosomes (LEs) is a rate-limiting step and a poorly defined process for productive intracellular ASO drug delivery. Here, we examined the role of Golgi-endosome transport, specifically M6PR shuttling mediated by GCC2, in PS-ASO trafficking and activity. We found that reduction in cellular levels of GCC2 or M6PR impaired PS-ASO release from endosomes and decreased PS-ASO activity in human cells. GCC2 relocated to LEs upon PS-ASO treatment, and M6PR also co-localized with PS-ASOs in LEs or on LE membranes. These proteins act through the same pathway to influence PS-ASO activity, with GCC2 action preceding that of M6PR. Our data indicate that M6PR binds PS-ASOs and facilitates their vesicular escape. The co-localization of M6PR and of GCC2 with ASOs is influenced by the PS modifications, which have been shown to enhance the affinity of ASOs for proteins, suggesting that localization of these proteins to LEs is mediated by ASO-protein interactions. Reduction of M6PR levels also decreased PS-ASO activity in mouse cells and in livers of mice treated subcutaneously with PS-ASO, indicating a conserved mechanism. Together, these results demonstrate that the transport machinery between LE and Golgi facilitates PS-ASO release. Oxford University Press 2020-02-20 2019-12-16 /pmc/articles/PMC7026651/ /pubmed/31840180 http://dx.doi.org/10.1093/nar/gkz1171 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Molecular Biology Liang, Xue-hai Sun, Hong Hsu, Chih-Wei Nichols, Joshua G Vickers, Timothy A De Hoyos, Cheryl L Crooke, Stanley T Golgi-endosome transport mediated by M6PR facilitates release of antisense oligonucleotides from endosomes |
title | Golgi-endosome transport mediated by M6PR facilitates release of antisense oligonucleotides from endosomes |
title_full | Golgi-endosome transport mediated by M6PR facilitates release of antisense oligonucleotides from endosomes |
title_fullStr | Golgi-endosome transport mediated by M6PR facilitates release of antisense oligonucleotides from endosomes |
title_full_unstemmed | Golgi-endosome transport mediated by M6PR facilitates release of antisense oligonucleotides from endosomes |
title_short | Golgi-endosome transport mediated by M6PR facilitates release of antisense oligonucleotides from endosomes |
title_sort | golgi-endosome transport mediated by m6pr facilitates release of antisense oligonucleotides from endosomes |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026651/ https://www.ncbi.nlm.nih.gov/pubmed/31840180 http://dx.doi.org/10.1093/nar/gkz1171 |
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