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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Japanese Association for Laboratory Animal Science
2014
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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. |
format | Online Article Text |
id | pubmed-4160937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Japanese Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
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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