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TonEBP and SMIT expression in human placenta

Tonicity-responsive enhancer binding protein (TonEBP) is a signal transcription factor of transporters such as sodium-myo-inositol cotransporter (SMIT), aldose reductase. TonEBP has a variety of functions such as control of intracellular osmolytes and immunomodulating. It is known that TonEBP is abu...

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Autores principales: Shin, Jung-A, Kwon, Hyug-Moo, Han, Ki-Hwan, Lee, Hwa-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Anatomists 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472141/
https://www.ncbi.nlm.nih.gov/pubmed/23094203
http://dx.doi.org/10.5115/acb.2012.45.3.155
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author Shin, Jung-A
Kwon, Hyug-Moo
Han, Ki-Hwan
Lee, Hwa-Young
author_facet Shin, Jung-A
Kwon, Hyug-Moo
Han, Ki-Hwan
Lee, Hwa-Young
author_sort Shin, Jung-A
collection PubMed
description Tonicity-responsive enhancer binding protein (TonEBP) is a signal transcription factor of transporters such as sodium-myo-inositol cotransporter (SMIT), aldose reductase. TonEBP has a variety of functions such as control of intracellular osmolytes and immunomodulating. It is known that TonEBP is abundant in the placenta, but location and function aren't known. The aim of this study is to describe the localization of TonEBP in the placenta. We assayed the immunohistochemistry of TonEBP and performed in situ hybridization of SMIT in normal human full term placenta. In normal human full term placenta, TonEBP was in villous trophoblasts, extravillous trophoblasts and some endothelial cells. The result of the in situ hybridization of SMIT was similar to that of immunohistochemistry of TonEBP. Neither TonEBP nor SMIT was present in TonEBP knockout mouse placenta. This shows TonEBP is a key factor in SMIT transcription. TonEBP may play an important role in transporting of inositol to fetus in placenta.
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spelling pubmed-34721412012-10-23 TonEBP and SMIT expression in human placenta Shin, Jung-A Kwon, Hyug-Moo Han, Ki-Hwan Lee, Hwa-Young Anat Cell Biol Original Article Tonicity-responsive enhancer binding protein (TonEBP) is a signal transcription factor of transporters such as sodium-myo-inositol cotransporter (SMIT), aldose reductase. TonEBP has a variety of functions such as control of intracellular osmolytes and immunomodulating. It is known that TonEBP is abundant in the placenta, but location and function aren't known. The aim of this study is to describe the localization of TonEBP in the placenta. We assayed the immunohistochemistry of TonEBP and performed in situ hybridization of SMIT in normal human full term placenta. In normal human full term placenta, TonEBP was in villous trophoblasts, extravillous trophoblasts and some endothelial cells. The result of the in situ hybridization of SMIT was similar to that of immunohistochemistry of TonEBP. Neither TonEBP nor SMIT was present in TonEBP knockout mouse placenta. This shows TonEBP is a key factor in SMIT transcription. TonEBP may play an important role in transporting of inositol to fetus in placenta. Korean Association of Anatomists 2012-09 2012-09-30 /pmc/articles/PMC3472141/ /pubmed/23094203 http://dx.doi.org/10.5115/acb.2012.45.3.155 Text en Copyright © 2012. Anatomy & Cell Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Shin, Jung-A
Kwon, Hyug-Moo
Han, Ki-Hwan
Lee, Hwa-Young
TonEBP and SMIT expression in human placenta
title TonEBP and SMIT expression in human placenta
title_full TonEBP and SMIT expression in human placenta
title_fullStr TonEBP and SMIT expression in human placenta
title_full_unstemmed TonEBP and SMIT expression in human placenta
title_short TonEBP and SMIT expression in human placenta
title_sort tonebp and smit expression in human placenta
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472141/
https://www.ncbi.nlm.nih.gov/pubmed/23094203
http://dx.doi.org/10.5115/acb.2012.45.3.155
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