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Experimental Evaluation of the Transport Mechanisms of PoIFN-α in Caco-2 Cells

For the development of an efficient intestinal delivery system for Porcine interferon-α (PoIFN-α), the understanding of transport mechanisms of which in the intestinal cell is essential. In this study, we investigated the absorption mechanisms of PoIFN-α in intestine cells. Caco-2 cells and fluoresc...

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Autores principales: Liu, Xin, Zheng, Sidi, Qin, Yue, Ding, Wenya, Tu, Yabin, Chen, Xingru, Wu, Yunzhou, Yanhua, Li, Cai, Xuehui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681924/
https://www.ncbi.nlm.nih.gov/pubmed/29163167
http://dx.doi.org/10.3389/fphar.2017.00781
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author Liu, Xin
Zheng, Sidi
Qin, Yue
Ding, Wenya
Tu, Yabin
Chen, Xingru
Wu, Yunzhou
Yanhua, Li
Cai, Xuehui
author_facet Liu, Xin
Zheng, Sidi
Qin, Yue
Ding, Wenya
Tu, Yabin
Chen, Xingru
Wu, Yunzhou
Yanhua, Li
Cai, Xuehui
author_sort Liu, Xin
collection PubMed
description For the development of an efficient intestinal delivery system for Porcine interferon-α (PoIFN-α), the understanding of transport mechanisms of which in the intestinal cell is essential. In this study, we investigated the absorption mechanisms of PoIFN-α in intestine cells. Caco-2 cells and fluorescein isothiocyanate-labeled (FITC)-PoIFN-α were used to explore the whole transport process, including endocytosis, intracellular trafficking, exocytosis, and transcytosis. Via various techniques, the transport pathways of PoIFN-α in Caco-2 cells and the mechanisms were clarified. Firstly, the endocytosis of PoIFN-α by Caco-2 cells was time, concentration and temperature dependence. And the lipid raft/caveolae endocytosis was the most likely endocytic pathway for PoIFN-α. Secondly, both Golgi apparatus and lysosome were involved in the intracellular trafficking of PoIFN-α. Thirdly, the treatment of indomethacin resulted in a significant decrease of exocytosis of PoIFN-α, indicating the participation of cyclooxygenase. Finally, to evaluate the efficiency of PoIFN-α transport, the transepithelial electrical resistance (TEER) value was measured to investigate the tight junctional integrity of the cell monolayers. The fluorescence microscope results revealed that the transport of PoIFN-α across the Caco-2 cell monolayers was restricted. In conclusion, this study depicts a probable picture of PoIFN-α transport in Caco-2 cells characterized by non-specificity, partial energy-dependency and low transcytosis.
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spelling pubmed-56819242017-11-21 Experimental Evaluation of the Transport Mechanisms of PoIFN-α in Caco-2 Cells Liu, Xin Zheng, Sidi Qin, Yue Ding, Wenya Tu, Yabin Chen, Xingru Wu, Yunzhou Yanhua, Li Cai, Xuehui Front Pharmacol Pharmacology For the development of an efficient intestinal delivery system for Porcine interferon-α (PoIFN-α), the understanding of transport mechanisms of which in the intestinal cell is essential. In this study, we investigated the absorption mechanisms of PoIFN-α in intestine cells. Caco-2 cells and fluorescein isothiocyanate-labeled (FITC)-PoIFN-α were used to explore the whole transport process, including endocytosis, intracellular trafficking, exocytosis, and transcytosis. Via various techniques, the transport pathways of PoIFN-α in Caco-2 cells and the mechanisms were clarified. Firstly, the endocytosis of PoIFN-α by Caco-2 cells was time, concentration and temperature dependence. And the lipid raft/caveolae endocytosis was the most likely endocytic pathway for PoIFN-α. Secondly, both Golgi apparatus and lysosome were involved in the intracellular trafficking of PoIFN-α. Thirdly, the treatment of indomethacin resulted in a significant decrease of exocytosis of PoIFN-α, indicating the participation of cyclooxygenase. Finally, to evaluate the efficiency of PoIFN-α transport, the transepithelial electrical resistance (TEER) value was measured to investigate the tight junctional integrity of the cell monolayers. The fluorescence microscope results revealed that the transport of PoIFN-α across the Caco-2 cell monolayers was restricted. In conclusion, this study depicts a probable picture of PoIFN-α transport in Caco-2 cells characterized by non-specificity, partial energy-dependency and low transcytosis. Frontiers Media S.A. 2017-11-07 /pmc/articles/PMC5681924/ /pubmed/29163167 http://dx.doi.org/10.3389/fphar.2017.00781 Text en Copyright © 2017 Liu, Zheng, Qin, Ding, Tu, Chen, Wu, Yanhua and Cai. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Liu, Xin
Zheng, Sidi
Qin, Yue
Ding, Wenya
Tu, Yabin
Chen, Xingru
Wu, Yunzhou
Yanhua, Li
Cai, Xuehui
Experimental Evaluation of the Transport Mechanisms of PoIFN-α in Caco-2 Cells
title Experimental Evaluation of the Transport Mechanisms of PoIFN-α in Caco-2 Cells
title_full Experimental Evaluation of the Transport Mechanisms of PoIFN-α in Caco-2 Cells
title_fullStr Experimental Evaluation of the Transport Mechanisms of PoIFN-α in Caco-2 Cells
title_full_unstemmed Experimental Evaluation of the Transport Mechanisms of PoIFN-α in Caco-2 Cells
title_short Experimental Evaluation of the Transport Mechanisms of PoIFN-α in Caco-2 Cells
title_sort experimental evaluation of the transport mechanisms of poifn-α in caco-2 cells
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681924/
https://www.ncbi.nlm.nih.gov/pubmed/29163167
http://dx.doi.org/10.3389/fphar.2017.00781
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