Accurate Determination of S-Phase Fraction in Proliferative Cells by Dual Fluorescence and Peroxidase Immunohistochemistry with 5-Bromo-2′-Deoxyuridine (BrdU) and Ki67 Antibodies

To ensure the maintenance of tissues in mammals, cell loss must be balanced with cell production, the proliferative activity being different from tissue to tissue. In this article, the authors propose a new method for the quantification of the proliferative activity, defined as the S-phase fraction...

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Published inThe journal of histochemistry and cytochemistry Vol. 59; no. 8; pp. 791 - 798
Main Authors Tanaka, Rina, Tainaka, Motomi, Ota, Takumi, Mizuguchi, Naoki, Kato, Hiroyuki, Urabe, Shoichi, Chen, Yulin, Fustin, Jean-Michel, Yamaguchi, Yoshiaki, Doi, Masao, Hamada, Shinshichi, Okamura, Hitoshi
Format Journal Article
LanguageEnglish
Published Los Angeles, CA SAGE Publications 01.08.2011
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ISSN0022-1554
1551-5044
1551-5044
DOI10.1369/0022155411411090

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Abstract To ensure the maintenance of tissues in mammals, cell loss must be balanced with cell production, the proliferative activity being different from tissue to tissue. In this article, the authors propose a new method for the quantification of the proliferative activity, defined as the S-phase fraction of actively cycling cells, by dual labeling with fluorescence and peroxidase immunohistochemistry using BrdU (marker of S-phase) and Ki67 antibodies (marker of G1-, S-, G2-, and M-phases) after a one-step antigen retrieval. In the generative cell zones of fundic and pyloric glandular stomachs, where the majority of cells were cycling, the authors measured a proliferative activity of 31%. In the epithelium of the forestomach and the skin, where cycling cells are intermingled with G0 and differentiated cells, proliferative activities were 21% and 13%, respectively. In the adrenal cortex, in which cycling cells were sparsely distributed, the proliferative activity reached 32%. During the regenerative process in the skin after a lesion, the proliferative activity increased in proximity to the wound. The present one-step dual-labeling method has revealed that the proliferative activity is different between tissues and depends on the physiological or pathological state.
AbstractList To ensure the maintenance of tissues in mammals, cell loss must be balanced with cell production, the proliferative activity being different from tissue to tissue. In this article, the authors propose a new method for the quantification of the proliferative activity, defined as the S-phase fraction of actively cycling cells, by dual labeling with fluorescence and peroxidase immunohistochemistry using BrdU (marker of S-phase) and Ki67 antibodies (marker of G1-, S-, G2-, and M-phases) after a one-step antigen retrieval. In the generative cell zones of fundic and pyloric glandular stomachs, where the majority of cells were cycling, the authors measured a proliferative activity of 31%. In the epithelium of the forestomach and the skin, where cycling cells are intermingled with G0 and differentiated cells, proliferative activities were 21% and 13%, respectively. In the adrenal cortex, in which cycling cells were sparsely distributed, the proliferative activity reached 32%. During the regenerative process in the skin after a lesion, the proliferative activity increased in proximity to the wound. The present one-step dual-labeling method has revealed that the proliferative activity is different between tissues and depends on the physiological or pathological state.
To ensure the maintenance of tissues in mammals, cell loss must be balanced with cell production, the proliferative activity being different from tissue to tissue. In this article, the authors propose a new method for the quantification of the proliferative activity, defined as the S-phase fraction of actively cycling cells, by dual labeling with fluorescence and peroxidase immunohistochemistry using BrdU (marker of S-phase) and Ki67 antibodies (marker of G(1)-, S-, G(2)-, and M-phases) after a one-step antigen retrieval. In the generative cell zones of fundic and pyloric glandular stomachs, where the majority of cells were cycling, the authors measured a proliferative activity of 31%. In the epithelium of the forestomach and the skin, where cycling cells are intermingled with G(0) and differentiated cells, proliferative activities were 21% and 13%, respectively. In the adrenal cortex, in which cycling cells were sparsely distributed, the proliferative activity reached 32%. During the regenerative process in the skin after a lesion, the proliferative activity increased in proximity to the wound. The present one-step dual-labeling method has revealed that the proliferative activity is different between tissues and depends on the physiological or pathological state.To ensure the maintenance of tissues in mammals, cell loss must be balanced with cell production, the proliferative activity being different from tissue to tissue. In this article, the authors propose a new method for the quantification of the proliferative activity, defined as the S-phase fraction of actively cycling cells, by dual labeling with fluorescence and peroxidase immunohistochemistry using BrdU (marker of S-phase) and Ki67 antibodies (marker of G(1)-, S-, G(2)-, and M-phases) after a one-step antigen retrieval. In the generative cell zones of fundic and pyloric glandular stomachs, where the majority of cells were cycling, the authors measured a proliferative activity of 31%. In the epithelium of the forestomach and the skin, where cycling cells are intermingled with G(0) and differentiated cells, proliferative activities were 21% and 13%, respectively. In the adrenal cortex, in which cycling cells were sparsely distributed, the proliferative activity reached 32%. During the regenerative process in the skin after a lesion, the proliferative activity increased in proximity to the wound. The present one-step dual-labeling method has revealed that the proliferative activity is different between tissues and depends on the physiological or pathological state.
To ensure the maintenance of tissues in mammals, cell loss must be balanced with cell production, the proliferative activity being different from tissue to tissue. In this article, the authors propose a new method for the quantification of the proliferative activity, defined as the S-phase fraction of actively cycling cells, by dual labeling with fluorescence and peroxidase immunohistochemistry using BrdU (marker of S-phase) and Ki67 antibodies (marker of G 1 -, S-, G 2 -, and M-phases) after a one-step antigen retrieval. In the generative cell zones of fundic and pyloric glandular stomachs, where the majority of cells were cycling, the authors measured a proliferative activity of 31%. In the epithelium of the forestomach and the skin, where cycling cells are intermingled with G 0 and differentiated cells, proliferative activities were 21% and 13%, respectively. In the adrenal cortex, in which cycling cells were sparsely distributed, the proliferative activity reached 32%. During the regenerative process in the skin after a lesion, the proliferative activity increased in proximity to the wound. The present one-step dual-labeling method has revealed that the proliferative activity is different between tissues and depends on the physiological or pathological state.
To ensure the maintenance of tissues in mammals, cell loss must be balanced with cell production, the proliferative activity being different from tissue to tissue. In this article, the authors propose a new method for the quantification of the proliferative activity, defined as the S-phase fraction of actively cycling cells, by dual labeling with fluorescence and peroxidase immunohistochemistry using BrdU (marker of S-phase) and Ki67 antibodies (marker of G 1 -, S-, G 2 -, and M-phases) after a one-step antigen retrieval. In the generative cell zones of fundic and pyloric glandular stomachs, where the majority of cells were cycling, the authors measured a proliferative activity of 31%. In the epithelium of the forestomach and the skin, where cycling cells are intermingled with G 0 and differentiated cells, proliferative activities were 21% and 13%, respectively. In the adrenal cortex, in which cycling cells were sparsely distributed, the proliferative activity reached 32%. During the regenerative process in the skin after a lesion, the proliferative activity increased in proximity to the wound. The present one-step dual-labeling method has revealed that the proliferative activity is different between tissues and depends on the physiological or pathological state.
Author Ota, Takumi
Mizuguchi, Naoki
Hamada, Shinshichi
Tanaka, Rina
Fustin, Jean-Michel
Tainaka, Motomi
Kato, Hiroyuki
Yamaguchi, Yoshiaki
Doi, Masao
Okamura, Hitoshi
Urabe, Shoichi
Chen, Yulin
AuthorAffiliation Department of Pathology, Kyoto Prefectural University of Medicine, Kyoto, Japan (SH)
Division of Pathology, Otsu Municipal Hospital, Otsu, Japan (SH)
Department of Systems Biology, Graduate School of Pharmacological Science, Kyoto University, Kyoto, Japan (RT,MT,TO,NM,HK,SU,YC,J-MF,YY,MD,HO)
AuthorAffiliation_xml – name: Department of Systems Biology, Graduate School of Pharmacological Science, Kyoto University, Kyoto, Japan (RT,MT,TO,NM,HK,SU,YC,J-MF,YY,MD,HO)
– name: Division of Pathology, Otsu Municipal Hospital, Otsu, Japan (SH)
– name: Department of Pathology, Kyoto Prefectural University of Medicine, Kyoto, Japan (SH)
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  email: okamurah@pharm.kyoto-u.ac.jp
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Keywords skin
stomach
adrenal gland
Ki67
fluorescence immunohistochemistry
BrdU
peroxidase immunohistochemistry
Language English
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Snippet To ensure the maintenance of tissues in mammals, cell loss must be balanced with cell production, the proliferative activity being different from tissue to...
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SubjectTerms Adrenal Glands - cytology
Adrenal Glands - metabolism
Animals
Antibodies
Bromodeoxyuridine
Cell Proliferation
Gastric Mucosa - cytology
Gastric Mucosa - metabolism
Immunohistochemistry
Indicators and Reagents
Ki-67 Antigen - metabolism
Male
Mice
Mice, Inbred C57BL
S Phase
Skin - cytology
Skin - injuries
Skin - metabolism
Staining and Labeling
Stomach - cytology
Stomach - metabolism
Wound Healing
Title Accurate Determination of S-Phase Fraction in Proliferative Cells by Dual Fluorescence and Peroxidase Immunohistochemistry with 5-Bromo-2′-Deoxyuridine (BrdU) and Ki67 Antibodies
URI https://journals.sagepub.com/doi/full/10.1369/0022155411411090
https://www.ncbi.nlm.nih.gov/pubmed/21551319
https://www.proquest.com/docview/880715282
https://pubmed.ncbi.nlm.nih.gov/PMC3261604
Volume 59
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