Cargando…

Antigen Delivery to Macrophages Using Liposomal Nanoparticles Targeting Sialoadhesin/CD169

Sialoadhesin (Sn, Siglec-1, CD169) is a member of the sialic acid binding Ig-like lectin (siglec) family expressed on macrophages. Its macrophage specific expression makes it an attractive target for delivering antigens to tissue macrophages via Sn-mediated endocytosis. Here we describe a novel appr...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Weihsu C., Kawasaki, Norihito, Nycholat, Corwin M., Han, Shoufa, Pilotte, Julie, Crocker, Paul R., Paulson, James C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378521/
https://www.ncbi.nlm.nih.gov/pubmed/22723922
http://dx.doi.org/10.1371/journal.pone.0039039
_version_ 1782236047801843712
author Chen, Weihsu C.
Kawasaki, Norihito
Nycholat, Corwin M.
Han, Shoufa
Pilotte, Julie
Crocker, Paul R.
Paulson, James C.
author_facet Chen, Weihsu C.
Kawasaki, Norihito
Nycholat, Corwin M.
Han, Shoufa
Pilotte, Julie
Crocker, Paul R.
Paulson, James C.
author_sort Chen, Weihsu C.
collection PubMed
description Sialoadhesin (Sn, Siglec-1, CD169) is a member of the sialic acid binding Ig-like lectin (siglec) family expressed on macrophages. Its macrophage specific expression makes it an attractive target for delivering antigens to tissue macrophages via Sn-mediated endocytosis. Here we describe a novel approach for delivering antigens to macrophages using liposomal nanoparticles displaying high affinity glycan ligands of Sn. The Sn-targeted liposomes selectively bind to and are internalized by Sn-expressing cells, and accumulate intracellularly over time. Our results show that ligand decorated liposomes are specific for Sn, since they are taken up by bone marrow derived macrophages that are derived from wild type but not Sn(−/−) mice. Importantly, the Sn-targeted liposomes dramatically enhance the delivery of antigens to macrophages for presentation to and proliferation of antigen-specific T cells. Together, these data provide insights into the potential of cell-specific targeting and delivery of antigens to intracellular organelles of macrophages using Sn-ligand decorated liposomal nanoparticles.
format Online
Article
Text
id pubmed-3378521
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-33785212012-06-21 Antigen Delivery to Macrophages Using Liposomal Nanoparticles Targeting Sialoadhesin/CD169 Chen, Weihsu C. Kawasaki, Norihito Nycholat, Corwin M. Han, Shoufa Pilotte, Julie Crocker, Paul R. Paulson, James C. PLoS One Research Article Sialoadhesin (Sn, Siglec-1, CD169) is a member of the sialic acid binding Ig-like lectin (siglec) family expressed on macrophages. Its macrophage specific expression makes it an attractive target for delivering antigens to tissue macrophages via Sn-mediated endocytosis. Here we describe a novel approach for delivering antigens to macrophages using liposomal nanoparticles displaying high affinity glycan ligands of Sn. The Sn-targeted liposomes selectively bind to and are internalized by Sn-expressing cells, and accumulate intracellularly over time. Our results show that ligand decorated liposomes are specific for Sn, since they are taken up by bone marrow derived macrophages that are derived from wild type but not Sn(−/−) mice. Importantly, the Sn-targeted liposomes dramatically enhance the delivery of antigens to macrophages for presentation to and proliferation of antigen-specific T cells. Together, these data provide insights into the potential of cell-specific targeting and delivery of antigens to intracellular organelles of macrophages using Sn-ligand decorated liposomal nanoparticles. Public Library of Science 2012-06-19 /pmc/articles/PMC3378521/ /pubmed/22723922 http://dx.doi.org/10.1371/journal.pone.0039039 Text en Chen et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chen, Weihsu C.
Kawasaki, Norihito
Nycholat, Corwin M.
Han, Shoufa
Pilotte, Julie
Crocker, Paul R.
Paulson, James C.
Antigen Delivery to Macrophages Using Liposomal Nanoparticles Targeting Sialoadhesin/CD169
title Antigen Delivery to Macrophages Using Liposomal Nanoparticles Targeting Sialoadhesin/CD169
title_full Antigen Delivery to Macrophages Using Liposomal Nanoparticles Targeting Sialoadhesin/CD169
title_fullStr Antigen Delivery to Macrophages Using Liposomal Nanoparticles Targeting Sialoadhesin/CD169
title_full_unstemmed Antigen Delivery to Macrophages Using Liposomal Nanoparticles Targeting Sialoadhesin/CD169
title_short Antigen Delivery to Macrophages Using Liposomal Nanoparticles Targeting Sialoadhesin/CD169
title_sort antigen delivery to macrophages using liposomal nanoparticles targeting sialoadhesin/cd169
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378521/
https://www.ncbi.nlm.nih.gov/pubmed/22723922
http://dx.doi.org/10.1371/journal.pone.0039039
work_keys_str_mv AT chenweihsuc antigendeliverytomacrophagesusingliposomalnanoparticlestargetingsialoadhesincd169
AT kawasakinorihito antigendeliverytomacrophagesusingliposomalnanoparticlestargetingsialoadhesincd169
AT nycholatcorwinm antigendeliverytomacrophagesusingliposomalnanoparticlestargetingsialoadhesincd169
AT hanshoufa antigendeliverytomacrophagesusingliposomalnanoparticlestargetingsialoadhesincd169
AT pilottejulie antigendeliverytomacrophagesusingliposomalnanoparticlestargetingsialoadhesincd169
AT crockerpaulr antigendeliverytomacrophagesusingliposomalnanoparticlestargetingsialoadhesincd169
AT paulsonjamesc antigendeliverytomacrophagesusingliposomalnanoparticlestargetingsialoadhesincd169