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Siglec-F is a novel intestinal M cell marker
Intestinal microfold (M) cells are epithelial cells primarily present on Peyer's patches (PPs) in the small intestine. The ability of M cells to shuttle antigens into the PP for appropriate immune responses makes M cells a target for next-generation oral vaccine delivery. In this regard, discov...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045273/ https://www.ncbi.nlm.nih.gov/pubmed/27524237 http://dx.doi.org/10.1016/j.bbrc.2016.08.055 |
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author | Gicheva, Nadezhda Macauley, Matthew S. Arlian, Britni M. Paulson, James C. Kawasaki, Norihito |
author_facet | Gicheva, Nadezhda Macauley, Matthew S. Arlian, Britni M. Paulson, James C. Kawasaki, Norihito |
author_sort | Gicheva, Nadezhda |
collection | PubMed |
description | Intestinal microfold (M) cells are epithelial cells primarily present on Peyer's patches (PPs) in the small intestine. The ability of M cells to shuttle antigens into the PP for appropriate immune responses makes M cells a target for next-generation oral vaccine delivery. In this regard, discovery of M cell-specific receptors are of great interest, which could act as molecular tags for targeted delivery of cargo to M cells. Here, using a monoclonal antibody we generated to the Sialic acid-binding immunoglobulin-like lectin F (Siglec-F), we show that Siglec-F is expressed on mouse M cells in the small intestine. Immunohistochemical analysis of the PP tissue sections shows that Siglec-F is expressed on the surface of the M cell membrane exposed to the intestinal lumen. Anti-Siglec-F antibody injected into the mouse small intestine bound to M cells, demonstrating the potential to target M cells via Siglec-F. |
format | Online Article Text |
id | pubmed-5045273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50452732016-10-07 Siglec-F is a novel intestinal M cell marker Gicheva, Nadezhda Macauley, Matthew S. Arlian, Britni M. Paulson, James C. Kawasaki, Norihito Biochem Biophys Res Commun Article Intestinal microfold (M) cells are epithelial cells primarily present on Peyer's patches (PPs) in the small intestine. The ability of M cells to shuttle antigens into the PP for appropriate immune responses makes M cells a target for next-generation oral vaccine delivery. In this regard, discovery of M cell-specific receptors are of great interest, which could act as molecular tags for targeted delivery of cargo to M cells. Here, using a monoclonal antibody we generated to the Sialic acid-binding immunoglobulin-like lectin F (Siglec-F), we show that Siglec-F is expressed on mouse M cells in the small intestine. Immunohistochemical analysis of the PP tissue sections shows that Siglec-F is expressed on the surface of the M cell membrane exposed to the intestinal lumen. Anti-Siglec-F antibody injected into the mouse small intestine bound to M cells, demonstrating the potential to target M cells via Siglec-F. Elsevier 2016-10-07 /pmc/articles/PMC5045273/ /pubmed/27524237 http://dx.doi.org/10.1016/j.bbrc.2016.08.055 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gicheva, Nadezhda Macauley, Matthew S. Arlian, Britni M. Paulson, James C. Kawasaki, Norihito Siglec-F is a novel intestinal M cell marker |
title | Siglec-F is a novel intestinal M cell marker |
title_full | Siglec-F is a novel intestinal M cell marker |
title_fullStr | Siglec-F is a novel intestinal M cell marker |
title_full_unstemmed | Siglec-F is a novel intestinal M cell marker |
title_short | Siglec-F is a novel intestinal M cell marker |
title_sort | siglec-f is a novel intestinal m cell marker |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045273/ https://www.ncbi.nlm.nih.gov/pubmed/27524237 http://dx.doi.org/10.1016/j.bbrc.2016.08.055 |
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