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Na(+)/HCO(3)(-) cotransporter is expressed on β and α cells during rat pancreatic development
AIM: To determine the expression and localization of the electrogenic Na(+)/HCO(3)(-) cotransporter (NBC1) in rat pancreas during development. METHODS: The rat pancreas from postnatal and embryos removed from the uterus of pregnant rats that had been sacrificed by CO(2) asphyxiation were used. Rat p...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116596/ https://www.ncbi.nlm.nih.gov/pubmed/27920473 http://dx.doi.org/10.3748/wjg.v22.i43.9525 |
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author | Cao, Li-Hua Xia, Cheng-Cai Shi, Zhao-Chun Wang, Ning Gu, Zheng-Hua Yu, Li-Zhi Wan, Qi De, Wei |
author_facet | Cao, Li-Hua Xia, Cheng-Cai Shi, Zhao-Chun Wang, Ning Gu, Zheng-Hua Yu, Li-Zhi Wan, Qi De, Wei |
author_sort | Cao, Li-Hua |
collection | PubMed |
description | AIM: To determine the expression and localization of the electrogenic Na(+)/HCO(3)(-) cotransporter (NBC1) in rat pancreas during development. METHODS: The rat pancreas from postnatal and embryos removed from the uterus of pregnant rats that had been sacrificed by CO(2) asphyxiation were used. Rat pancreas from embryonic day (E) 15.5 and E18.5 rat embryos was isolated under a stereomicroscope. Rat pancreas from postnatal (P) days 0, 7, 14, 21 and adult was directly isolated by the unaided eye. The RT-PCR analysis of the NBC1 specific region on rat pancreas tissues from different developmental stages. The two antibodies which target the NBC1 common COOH-terminal region and NH(2)-terminal region detected a clear band of about 145 kDa in the Western blot analysis. The localization of NBC1 was examined by immuno-fluorescence detection. RESULTS: The results revealed the first peak of NBC1 expression at E18.5 and the second peak at P14. Meanwhile, the low NBC1 expression occurred at P7 and adult stages. Our results demonstrated, for the first time, the presence of NBC1 in the plasma membrane of β and α cells, as well as in the basolateral membrane of acinar cells of the rat pancreas at different stages of development. CONCLUSION: The data strongly suggests that NBC1 is diversely expressed in the pancreas at different developmental stages, where it may exert its functions in pancreatic development especially islet cell growth through HCO(3)(-) transport and pH regulation. |
format | Online Article Text |
id | pubmed-5116596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-51165962016-12-05 Na(+)/HCO(3)(-) cotransporter is expressed on β and α cells during rat pancreatic development Cao, Li-Hua Xia, Cheng-Cai Shi, Zhao-Chun Wang, Ning Gu, Zheng-Hua Yu, Li-Zhi Wan, Qi De, Wei World J Gastroenterol Basic Study AIM: To determine the expression and localization of the electrogenic Na(+)/HCO(3)(-) cotransporter (NBC1) in rat pancreas during development. METHODS: The rat pancreas from postnatal and embryos removed from the uterus of pregnant rats that had been sacrificed by CO(2) asphyxiation were used. Rat pancreas from embryonic day (E) 15.5 and E18.5 rat embryos was isolated under a stereomicroscope. Rat pancreas from postnatal (P) days 0, 7, 14, 21 and adult was directly isolated by the unaided eye. The RT-PCR analysis of the NBC1 specific region on rat pancreas tissues from different developmental stages. The two antibodies which target the NBC1 common COOH-terminal region and NH(2)-terminal region detected a clear band of about 145 kDa in the Western blot analysis. The localization of NBC1 was examined by immuno-fluorescence detection. RESULTS: The results revealed the first peak of NBC1 expression at E18.5 and the second peak at P14. Meanwhile, the low NBC1 expression occurred at P7 and adult stages. Our results demonstrated, for the first time, the presence of NBC1 in the plasma membrane of β and α cells, as well as in the basolateral membrane of acinar cells of the rat pancreas at different stages of development. CONCLUSION: The data strongly suggests that NBC1 is diversely expressed in the pancreas at different developmental stages, where it may exert its functions in pancreatic development especially islet cell growth through HCO(3)(-) transport and pH regulation. Baishideng Publishing Group Inc 2016-11-21 2016-11-21 /pmc/articles/PMC5116596/ /pubmed/27920473 http://dx.doi.org/10.3748/wjg.v22.i43.9525 Text en ©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Basic Study Cao, Li-Hua Xia, Cheng-Cai Shi, Zhao-Chun Wang, Ning Gu, Zheng-Hua Yu, Li-Zhi Wan, Qi De, Wei Na(+)/HCO(3)(-) cotransporter is expressed on β and α cells during rat pancreatic development |
title | Na(+)/HCO(3)(-) cotransporter is expressed on β and α cells during rat pancreatic development |
title_full | Na(+)/HCO(3)(-) cotransporter is expressed on β and α cells during rat pancreatic development |
title_fullStr | Na(+)/HCO(3)(-) cotransporter is expressed on β and α cells during rat pancreatic development |
title_full_unstemmed | Na(+)/HCO(3)(-) cotransporter is expressed on β and α cells during rat pancreatic development |
title_short | Na(+)/HCO(3)(-) cotransporter is expressed on β and α cells during rat pancreatic development |
title_sort | na(+)/hco(3)(-) cotransporter is expressed on β and α cells during rat pancreatic development |
topic | Basic Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116596/ https://www.ncbi.nlm.nih.gov/pubmed/27920473 http://dx.doi.org/10.3748/wjg.v22.i43.9525 |
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