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Establishment of a mast cell line, NCL-2, without Kit mutation, derived from NC mouse bone marrow
Immortal mast cell lines, such as RBL-2H3 and HMC-1 cells, are commonly utilized to investigate the function of mast cells. However, they are tumor cells carrying a gain-of-function mutation of Kit. We established an immortal mast cell line without Kit mutation, NCL-2, derived from NC mouse bone mar...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4050185/ https://www.ncbi.nlm.nih.gov/pubmed/24918047 http://dx.doi.org/10.1016/j.fob.2014.03.011 |
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author | Hiragun, Takaaki Yanase, Yuhki Okabe, Tsutomu Hiragun, Makiko Kawai, Mikio Hide, Michihiro |
author_facet | Hiragun, Takaaki Yanase, Yuhki Okabe, Tsutomu Hiragun, Makiko Kawai, Mikio Hide, Michihiro |
author_sort | Hiragun, Takaaki |
collection | PubMed |
description | Immortal mast cell lines, such as RBL-2H3 and HMC-1 cells, are commonly utilized to investigate the function of mast cells. However, they are tumor cells carrying a gain-of-function mutation of Kit. We established an immortal mast cell line without Kit mutation, NCL-2, derived from NC mouse bone marrow. NCL-2 cells could be maintained without additional growth factors and thus could respond to exogenous growth signals. Moreover, NCL-2 cells expressed FcεRI and KIT, and release histamine and LTB(4) in response to antigen stimulation. This cell line could be a useful tool to analyze proliferation, differentiation, and function of normal mast cells. |
format | Online Article Text |
id | pubmed-4050185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-40501852014-06-10 Establishment of a mast cell line, NCL-2, without Kit mutation, derived from NC mouse bone marrow Hiragun, Takaaki Yanase, Yuhki Okabe, Tsutomu Hiragun, Makiko Kawai, Mikio Hide, Michihiro FEBS Open Bio Article Immortal mast cell lines, such as RBL-2H3 and HMC-1 cells, are commonly utilized to investigate the function of mast cells. However, they are tumor cells carrying a gain-of-function mutation of Kit. We established an immortal mast cell line without Kit mutation, NCL-2, derived from NC mouse bone marrow. NCL-2 cells could be maintained without additional growth factors and thus could respond to exogenous growth signals. Moreover, NCL-2 cells expressed FcεRI and KIT, and release histamine and LTB(4) in response to antigen stimulation. This cell line could be a useful tool to analyze proliferation, differentiation, and function of normal mast cells. Elsevier 2014-04-02 /pmc/articles/PMC4050185/ /pubmed/24918047 http://dx.doi.org/10.1016/j.fob.2014.03.011 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Article Hiragun, Takaaki Yanase, Yuhki Okabe, Tsutomu Hiragun, Makiko Kawai, Mikio Hide, Michihiro Establishment of a mast cell line, NCL-2, without Kit mutation, derived from NC mouse bone marrow |
title | Establishment of a mast cell line, NCL-2, without Kit mutation, derived from NC mouse bone marrow |
title_full | Establishment of a mast cell line, NCL-2, without Kit mutation, derived from NC mouse bone marrow |
title_fullStr | Establishment of a mast cell line, NCL-2, without Kit mutation, derived from NC mouse bone marrow |
title_full_unstemmed | Establishment of a mast cell line, NCL-2, without Kit mutation, derived from NC mouse bone marrow |
title_short | Establishment of a mast cell line, NCL-2, without Kit mutation, derived from NC mouse bone marrow |
title_sort | establishment of a mast cell line, ncl-2, without kit mutation, derived from nc mouse bone marrow |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4050185/ https://www.ncbi.nlm.nih.gov/pubmed/24918047 http://dx.doi.org/10.1016/j.fob.2014.03.011 |
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