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PNA lectin for purifying mouse acinar cells from the inflamed pancreas
Better methods for purifying human or mouse acinar cells without the need for genetic modification are needed. Such techniques would be advantageous for the specific study of certain mechanisms, such as acinar-to-beta-cell reprogramming and pancreatitis. Ulex Europaeus Agglutinin I (UEA-I) lectin ha...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756371/ https://www.ncbi.nlm.nih.gov/pubmed/26884345 http://dx.doi.org/10.1038/srep21127 |
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author | Xiao, Xiangwei Fischbach, Shane Fusco, Joseph Zimmerman, Ray Song, Zewen Nebres, Philip Ricks, David Matthew Prasadan, Krishna Shiota, Chiyo Husain, Sohail Z. Gittes, George K. |
author_facet | Xiao, Xiangwei Fischbach, Shane Fusco, Joseph Zimmerman, Ray Song, Zewen Nebres, Philip Ricks, David Matthew Prasadan, Krishna Shiota, Chiyo Husain, Sohail Z. Gittes, George K. |
author_sort | Xiao, Xiangwei |
collection | PubMed |
description | Better methods for purifying human or mouse acinar cells without the need for genetic modification are needed. Such techniques would be advantageous for the specific study of certain mechanisms, such as acinar-to-beta-cell reprogramming and pancreatitis. Ulex Europaeus Agglutinin I (UEA-I) lectin has been used to label and isolate acinar cells from the pancreas. However, the purity of the UEA-I-positive cell fraction has not been fully evaluated. Here, we screened 20 widely used lectins for their binding specificity for major pancreatic cell types, and found that UEA-I and Peanut agglutinin (PNA) have a specific affinity for acinar cells in the mouse pancreas, with minimal affinity for other major pancreatic cell types including endocrine cells, duct cells and endothelial cells. Moreover, PNA-purified acinar cells were less contaminated with mesenchymal and inflammatory cells, compared to UEA-I purified acinar cells. Thus, UEA-I and PNA appear to be excellent lectins for pancreatic acinar cell purification. PNA may be a better choice in situations where mesenchymal cells or inflammatory cells are significantly increased in the pancreas, such as type 1 diabetes, pancreatitis and pancreatic cancer. |
format | Online Article Text |
id | pubmed-4756371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47563712016-02-25 PNA lectin for purifying mouse acinar cells from the inflamed pancreas Xiao, Xiangwei Fischbach, Shane Fusco, Joseph Zimmerman, Ray Song, Zewen Nebres, Philip Ricks, David Matthew Prasadan, Krishna Shiota, Chiyo Husain, Sohail Z. Gittes, George K. Sci Rep Article Better methods for purifying human or mouse acinar cells without the need for genetic modification are needed. Such techniques would be advantageous for the specific study of certain mechanisms, such as acinar-to-beta-cell reprogramming and pancreatitis. Ulex Europaeus Agglutinin I (UEA-I) lectin has been used to label and isolate acinar cells from the pancreas. However, the purity of the UEA-I-positive cell fraction has not been fully evaluated. Here, we screened 20 widely used lectins for their binding specificity for major pancreatic cell types, and found that UEA-I and Peanut agglutinin (PNA) have a specific affinity for acinar cells in the mouse pancreas, with minimal affinity for other major pancreatic cell types including endocrine cells, duct cells and endothelial cells. Moreover, PNA-purified acinar cells were less contaminated with mesenchymal and inflammatory cells, compared to UEA-I purified acinar cells. Thus, UEA-I and PNA appear to be excellent lectins for pancreatic acinar cell purification. PNA may be a better choice in situations where mesenchymal cells or inflammatory cells are significantly increased in the pancreas, such as type 1 diabetes, pancreatitis and pancreatic cancer. Nature Publishing Group 2016-02-17 /pmc/articles/PMC4756371/ /pubmed/26884345 http://dx.doi.org/10.1038/srep21127 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Xiao, Xiangwei Fischbach, Shane Fusco, Joseph Zimmerman, Ray Song, Zewen Nebres, Philip Ricks, David Matthew Prasadan, Krishna Shiota, Chiyo Husain, Sohail Z. Gittes, George K. PNA lectin for purifying mouse acinar cells from the inflamed pancreas |
title | PNA lectin for purifying mouse acinar cells from the inflamed pancreas |
title_full | PNA lectin for purifying mouse acinar cells from the inflamed pancreas |
title_fullStr | PNA lectin for purifying mouse acinar cells from the inflamed pancreas |
title_full_unstemmed | PNA lectin for purifying mouse acinar cells from the inflamed pancreas |
title_short | PNA lectin for purifying mouse acinar cells from the inflamed pancreas |
title_sort | pna lectin for purifying mouse acinar cells from the inflamed pancreas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756371/ https://www.ncbi.nlm.nih.gov/pubmed/26884345 http://dx.doi.org/10.1038/srep21127 |
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