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Multivalent Conjugation of Antibody to Dendrimers for the Enhanced Capture and Regulation on Colon Cancer Cells

Circulation tumor cells (CTCs) in the bloodstream of early-stage cancer patients carry the important information about valuable biomarkers and biological properties of primary tumor. However, detection and capture of CTCs are challenging owing to their low concentrations. Traditional technologies ha...

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Autores principales: Xie, Jingjing, Wang, Jichuang, Chen, Hongning, Shen, Weiyu, Sinko, Patrick J., Dong, Haiyan, Zhao, Rongli, Lu, Yusheng, Zhu, Yewei, Jia, Lee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377633/
https://www.ncbi.nlm.nih.gov/pubmed/25819426
http://dx.doi.org/10.1038/srep09445
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author Xie, Jingjing
Wang, Jichuang
Chen, Hongning
Shen, Weiyu
Sinko, Patrick J.
Dong, Haiyan
Zhao, Rongli
Lu, Yusheng
Zhu, Yewei
Jia, Lee
author_facet Xie, Jingjing
Wang, Jichuang
Chen, Hongning
Shen, Weiyu
Sinko, Patrick J.
Dong, Haiyan
Zhao, Rongli
Lu, Yusheng
Zhu, Yewei
Jia, Lee
author_sort Xie, Jingjing
collection PubMed
description Circulation tumor cells (CTCs) in the bloodstream of early-stage cancer patients carry the important information about valuable biomarkers and biological properties of primary tumor. However, detection and capture of CTCs are challenging owing to their low concentrations. Traditional technologies have the limited detection sensitivity and the low capture efficiency. We, herein, report an effective approach to specifically bind and capture colon cancer HT29 cells by using multiple Sialyl Lewis X antibodies (aSlex)-conjugated PAMAM dendrimers. The conjugation was characterized by using atom force microscope, UV and fluorescence measurements. The capturing and regulating HT29 cells by the aSlex-coated dendrimer conjugate were analyzed by microscopy and flow cytometry. The results indicated that the conjugate showed the enhanced capture of HT29 cells in a concentration-dependent manner and the maximum capture efficiency of 77.88% was obtained within 1 h-exposure. G6-5aSlex-FITC conjugate showed capture efficiency better than FITC-G6-COOH-5aSlex conjugate. G6-5aSlex-FITC conjugate could specifically capture HT29 cells even when the target HT29 cells were diluted with the interfering cells (e.g., RBCs) to a low concentration. The capture resulted in a concentration-dependent restraint of the cell activity. In conclusion, the aSlex-coated dendrimer conjugate displayed the great potential in capturing and restraining colorectal CTCs in blood.
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spelling pubmed-43776332015-04-07 Multivalent Conjugation of Antibody to Dendrimers for the Enhanced Capture and Regulation on Colon Cancer Cells Xie, Jingjing Wang, Jichuang Chen, Hongning Shen, Weiyu Sinko, Patrick J. Dong, Haiyan Zhao, Rongli Lu, Yusheng Zhu, Yewei Jia, Lee Sci Rep Article Circulation tumor cells (CTCs) in the bloodstream of early-stage cancer patients carry the important information about valuable biomarkers and biological properties of primary tumor. However, detection and capture of CTCs are challenging owing to their low concentrations. Traditional technologies have the limited detection sensitivity and the low capture efficiency. We, herein, report an effective approach to specifically bind and capture colon cancer HT29 cells by using multiple Sialyl Lewis X antibodies (aSlex)-conjugated PAMAM dendrimers. The conjugation was characterized by using atom force microscope, UV and fluorescence measurements. The capturing and regulating HT29 cells by the aSlex-coated dendrimer conjugate were analyzed by microscopy and flow cytometry. The results indicated that the conjugate showed the enhanced capture of HT29 cells in a concentration-dependent manner and the maximum capture efficiency of 77.88% was obtained within 1 h-exposure. G6-5aSlex-FITC conjugate showed capture efficiency better than FITC-G6-COOH-5aSlex conjugate. G6-5aSlex-FITC conjugate could specifically capture HT29 cells even when the target HT29 cells were diluted with the interfering cells (e.g., RBCs) to a low concentration. The capture resulted in a concentration-dependent restraint of the cell activity. In conclusion, the aSlex-coated dendrimer conjugate displayed the great potential in capturing and restraining colorectal CTCs in blood. Nature Publishing Group 2015-03-30 /pmc/articles/PMC4377633/ /pubmed/25819426 http://dx.doi.org/10.1038/srep09445 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Xie, Jingjing
Wang, Jichuang
Chen, Hongning
Shen, Weiyu
Sinko, Patrick J.
Dong, Haiyan
Zhao, Rongli
Lu, Yusheng
Zhu, Yewei
Jia, Lee
Multivalent Conjugation of Antibody to Dendrimers for the Enhanced Capture and Regulation on Colon Cancer Cells
title Multivalent Conjugation of Antibody to Dendrimers for the Enhanced Capture and Regulation on Colon Cancer Cells
title_full Multivalent Conjugation of Antibody to Dendrimers for the Enhanced Capture and Regulation on Colon Cancer Cells
title_fullStr Multivalent Conjugation of Antibody to Dendrimers for the Enhanced Capture and Regulation on Colon Cancer Cells
title_full_unstemmed Multivalent Conjugation of Antibody to Dendrimers for the Enhanced Capture and Regulation on Colon Cancer Cells
title_short Multivalent Conjugation of Antibody to Dendrimers for the Enhanced Capture and Regulation on Colon Cancer Cells
title_sort multivalent conjugation of antibody to dendrimers for the enhanced capture and regulation on colon cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377633/
https://www.ncbi.nlm.nih.gov/pubmed/25819426
http://dx.doi.org/10.1038/srep09445
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