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Establishment of CMab-43, a Sensitive and Specific Anti-CD133 Monoclonal Antibody, for Immunohistochemistry

CD133, also known as prominin-1, was first described as a cell surface marker on early progenitor and hematopoietic stem cells. It is a five-domain transmembrane protein composed of an N-terminal extracellular tail, two small cytoplasmic loops, two large extracellular loops containing seven potentia...

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Autores principales: Itai, Shunsuke, Fujii, Yuki, Nakamura, Takuro, Chang, Yao-Wen, Yanaka, Miyuki, Saidoh, Noriko, Handa, Saori, Suzuki, Hiroyoshi, Harada, Hiroyuki, Yamada, Shinji, Kaneko, Mika K., Kato, Yukinari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975129/
https://www.ncbi.nlm.nih.gov/pubmed/28910211
http://dx.doi.org/10.1089/mab.2017.0031
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author Itai, Shunsuke
Fujii, Yuki
Nakamura, Takuro
Chang, Yao-Wen
Yanaka, Miyuki
Saidoh, Noriko
Handa, Saori
Suzuki, Hiroyoshi
Harada, Hiroyuki
Yamada, Shinji
Kaneko, Mika K.
Kato, Yukinari
author_facet Itai, Shunsuke
Fujii, Yuki
Nakamura, Takuro
Chang, Yao-Wen
Yanaka, Miyuki
Saidoh, Noriko
Handa, Saori
Suzuki, Hiroyoshi
Harada, Hiroyuki
Yamada, Shinji
Kaneko, Mika K.
Kato, Yukinari
author_sort Itai, Shunsuke
collection PubMed
description CD133, also known as prominin-1, was first described as a cell surface marker on early progenitor and hematopoietic stem cells. It is a five-domain transmembrane protein composed of an N-terminal extracellular tail, two small cytoplasmic loops, two large extracellular loops containing seven potential glycosylation sites, and a short C-terminal intracellular tail. CD133 has been used as a marker to identify cancer stem cells derived from primary solid tumors and as a prognostic marker of gliomas. Herein, we developed novel anti-CD133 monoclonal antibodies (mAbs) and characterized their efficacy in flow cytometry, Western blot, and immunohistochemical analyses. We expressed the full length of CD133 in LN229 glioblastoma cells, immunized mice with LN229/CD133 cells, and performed the first screening using flow cytometry. After limiting dilution, we established 100 anti-CD133 mAbs, reacting with LN229/CD133 cells but not with LN229 cells. Subsequently, we performed the second and third screening with Western blot and immunohistochemical analyses, respectively. Among 100 mAbs, 11 strongly reacted with CD133 in Western blot analysis. One of 11 clones, CMab-43 (IgG(2a), kappa), showed a sensitive and specific reaction against colon cancer cells, warranting the use of CMab-43 in detecting CD133 in pathological analyses of CD133-expressing cancers.
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spelling pubmed-69751292020-01-23 Establishment of CMab-43, a Sensitive and Specific Anti-CD133 Monoclonal Antibody, for Immunohistochemistry Itai, Shunsuke Fujii, Yuki Nakamura, Takuro Chang, Yao-Wen Yanaka, Miyuki Saidoh, Noriko Handa, Saori Suzuki, Hiroyoshi Harada, Hiroyuki Yamada, Shinji Kaneko, Mika K. Kato, Yukinari Monoclon Antib Immunodiagn Immunother Original Articles CD133, also known as prominin-1, was first described as a cell surface marker on early progenitor and hematopoietic stem cells. It is a five-domain transmembrane protein composed of an N-terminal extracellular tail, two small cytoplasmic loops, two large extracellular loops containing seven potential glycosylation sites, and a short C-terminal intracellular tail. CD133 has been used as a marker to identify cancer stem cells derived from primary solid tumors and as a prognostic marker of gliomas. Herein, we developed novel anti-CD133 monoclonal antibodies (mAbs) and characterized their efficacy in flow cytometry, Western blot, and immunohistochemical analyses. We expressed the full length of CD133 in LN229 glioblastoma cells, immunized mice with LN229/CD133 cells, and performed the first screening using flow cytometry. After limiting dilution, we established 100 anti-CD133 mAbs, reacting with LN229/CD133 cells but not with LN229 cells. Subsequently, we performed the second and third screening with Western blot and immunohistochemical analyses, respectively. Among 100 mAbs, 11 strongly reacted with CD133 in Western blot analysis. One of 11 clones, CMab-43 (IgG(2a), kappa), showed a sensitive and specific reaction against colon cancer cells, warranting the use of CMab-43 in detecting CD133 in pathological analyses of CD133-expressing cancers. Mary Ann Liebert, Inc., publishers 2017-10-01 2017-10-01 /pmc/articles/PMC6975129/ /pubmed/28910211 http://dx.doi.org/10.1089/mab.2017.0031 Text en © Shunsuke Itai et al. 2017; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Itai, Shunsuke
Fujii, Yuki
Nakamura, Takuro
Chang, Yao-Wen
Yanaka, Miyuki
Saidoh, Noriko
Handa, Saori
Suzuki, Hiroyoshi
Harada, Hiroyuki
Yamada, Shinji
Kaneko, Mika K.
Kato, Yukinari
Establishment of CMab-43, a Sensitive and Specific Anti-CD133 Monoclonal Antibody, for Immunohistochemistry
title Establishment of CMab-43, a Sensitive and Specific Anti-CD133 Monoclonal Antibody, for Immunohistochemistry
title_full Establishment of CMab-43, a Sensitive and Specific Anti-CD133 Monoclonal Antibody, for Immunohistochemistry
title_fullStr Establishment of CMab-43, a Sensitive and Specific Anti-CD133 Monoclonal Antibody, for Immunohistochemistry
title_full_unstemmed Establishment of CMab-43, a Sensitive and Specific Anti-CD133 Monoclonal Antibody, for Immunohistochemistry
title_short Establishment of CMab-43, a Sensitive and Specific Anti-CD133 Monoclonal Antibody, for Immunohistochemistry
title_sort establishment of cmab-43, a sensitive and specific anti-cd133 monoclonal antibody, for immunohistochemistry
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975129/
https://www.ncbi.nlm.nih.gov/pubmed/28910211
http://dx.doi.org/10.1089/mab.2017.0031
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