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Generation and Analysis of Serine Protease Inhibitor Kazal Type 3-Cre Driver Mice

Serine protease inhibitor Kazal type 1 (SPINK1; mouse homologue Spink3) was initially discovered as a trypsin-specific inhibitor in the pancreas. However, previous studies have suggested that SPINK1/Spink3 is expressed in a wide range of normal tissues and tumors, although precise characterization o...

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Autores principales: Sakata, Kazuya, Ohmuraya, Masaki, Araki, Kimi, Suzuki, Chigure, Ida, Satoshi, Hashimoto, Daisuke, Wang, Jung, Uchiyama, Yasuo, Baba, Hideo, Yamamura, Ken-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Association for Laboratory Animal Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160937/
https://www.ncbi.nlm.nih.gov/pubmed/24521862
http://dx.doi.org/10.1538/expanim.63.45
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author Sakata, Kazuya
Ohmuraya, Masaki
Araki, Kimi
Suzuki, Chigure
Ida, Satoshi
Hashimoto, Daisuke
Wang, Jung
Uchiyama, Yasuo
Baba, Hideo
Yamamura, Ken-ichi
author_facet Sakata, Kazuya
Ohmuraya, Masaki
Araki, Kimi
Suzuki, Chigure
Ida, Satoshi
Hashimoto, Daisuke
Wang, Jung
Uchiyama, Yasuo
Baba, Hideo
Yamamura, Ken-ichi
author_sort Sakata, Kazuya
collection PubMed
description Serine protease inhibitor Kazal type 1 (SPINK1; mouse homologue Spink3) was initially discovered as a trypsin-specific inhibitor in the pancreas. However, previous studies have suggested that SPINK1/Spink3 is expressed in a wide range of normal tissues and tumors, although precise characterization of its gene expression has not been described in adulthood. To further analyze Spink3 expression, we generated two mouse lines in which either lacZ or Cre recombinase genes were inserted into the Spink3 locus by Cre-loxP technology. In Spink3(lacZ) mice, β-galactosidase activity was found in acinar cells of the pancreas and kidney, as well as epithelial cells of the bronchus in the lung, but not in the gastrointestinal tract or liver. Spink3(cre) knock-in mice were crossed with Rosa26 reporter (R26R) mice to monitor Spink3 promoter activity. In Spink3(cre);R26R mice, β-galactosidase activity was found in acinar cells of the pancreas, kidney, lung, and a small proportion of cells in the gastrointestinal tract and liver. These data suggest that Spink3 is widely expressed in endoderm-derived tissues, and that Spink3(cre) knock-in mice are a useful tool for establishment of a conditional knockout mice to analyze Spink3 function not only in normal tissues, but also in tumors that express SPINK1/Spink3.
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spelling pubmed-41609372014-10-21 Generation and Analysis of Serine Protease Inhibitor Kazal Type 3-Cre Driver Mice Sakata, Kazuya Ohmuraya, Masaki Araki, Kimi Suzuki, Chigure Ida, Satoshi Hashimoto, Daisuke Wang, Jung Uchiyama, Yasuo Baba, Hideo Yamamura, Ken-ichi Exp Anim Original Serine protease inhibitor Kazal type 1 (SPINK1; mouse homologue Spink3) was initially discovered as a trypsin-specific inhibitor in the pancreas. However, previous studies have suggested that SPINK1/Spink3 is expressed in a wide range of normal tissues and tumors, although precise characterization of its gene expression has not been described in adulthood. To further analyze Spink3 expression, we generated two mouse lines in which either lacZ or Cre recombinase genes were inserted into the Spink3 locus by Cre-loxP technology. In Spink3(lacZ) mice, β-galactosidase activity was found in acinar cells of the pancreas and kidney, as well as epithelial cells of the bronchus in the lung, but not in the gastrointestinal tract or liver. Spink3(cre) knock-in mice were crossed with Rosa26 reporter (R26R) mice to monitor Spink3 promoter activity. In Spink3(cre);R26R mice, β-galactosidase activity was found in acinar cells of the pancreas, kidney, lung, and a small proportion of cells in the gastrointestinal tract and liver. These data suggest that Spink3 is widely expressed in endoderm-derived tissues, and that Spink3(cre) knock-in mice are a useful tool for establishment of a conditional knockout mice to analyze Spink3 function not only in normal tissues, but also in tumors that express SPINK1/Spink3. Japanese Association for Laboratory Animal Science 2014-02-07 2014 /pmc/articles/PMC4160937/ /pubmed/24521862 http://dx.doi.org/10.1538/expanim.63.45 Text en ©2014 Japanese Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original
Sakata, Kazuya
Ohmuraya, Masaki
Araki, Kimi
Suzuki, Chigure
Ida, Satoshi
Hashimoto, Daisuke
Wang, Jung
Uchiyama, Yasuo
Baba, Hideo
Yamamura, Ken-ichi
Generation and Analysis of Serine Protease Inhibitor Kazal Type 3-Cre Driver Mice
title Generation and Analysis of Serine Protease Inhibitor Kazal Type 3-Cre Driver Mice
title_full Generation and Analysis of Serine Protease Inhibitor Kazal Type 3-Cre Driver Mice
title_fullStr Generation and Analysis of Serine Protease Inhibitor Kazal Type 3-Cre Driver Mice
title_full_unstemmed Generation and Analysis of Serine Protease Inhibitor Kazal Type 3-Cre Driver Mice
title_short Generation and Analysis of Serine Protease Inhibitor Kazal Type 3-Cre Driver Mice
title_sort generation and analysis of serine protease inhibitor kazal type 3-cre driver mice
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160937/
https://www.ncbi.nlm.nih.gov/pubmed/24521862
http://dx.doi.org/10.1538/expanim.63.45
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