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 in | The journal of histochemistry and cytochemistry Vol. 59; no. 8; pp. 791 - 798 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Los Angeles, CA
SAGE Publications
01.08.2011
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Subjects | |
Online Access | Get full text |
ISSN | 0022-1554 1551-5044 1551-5044 |
DOI | 10.1369/0022155411411090 |
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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. |
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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) |
Author_xml | – sequence: 1 givenname: Rina surname: Tanaka fullname: Tanaka, Rina – sequence: 2 givenname: Motomi surname: Tainaka fullname: Tainaka, Motomi – sequence: 3 givenname: Takumi surname: Ota fullname: Ota, Takumi – sequence: 4 givenname: Naoki surname: Mizuguchi fullname: Mizuguchi, Naoki – sequence: 5 givenname: Hiroyuki surname: Kato fullname: Kato, Hiroyuki – sequence: 6 givenname: Shoichi surname: Urabe fullname: Urabe, Shoichi – sequence: 7 givenname: Yulin surname: Chen fullname: Chen, Yulin – sequence: 8 givenname: Jean-Michel surname: Fustin fullname: Fustin, Jean-Michel – sequence: 9 givenname: Yoshiaki surname: Yamaguchi fullname: Yamaguchi, Yoshiaki – sequence: 10 givenname: Masao surname: Doi fullname: Doi, Masao – sequence: 11 givenname: Shinshichi surname: Hamada fullname: Hamada, Shinshichi – sequence: 12 givenname: Hitoshi surname: Okamura fullname: Okamura, Hitoshi email: okamurah@pharm.kyoto-u.ac.jp |
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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 |
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