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Expression of human milk fat globulin proteins in cells of haemopoietic origin
Lineage-specific gene expression has been used for the identification of metastasis of cancers with unknown primary site or of disseminated cancer cells in haemopoietic compartments such as bone marrow or in lymph nodes. For the muc1, cytokeratin-19 and the CEA genes, the transcription in haemopoiet...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2000
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374676/ https://www.ncbi.nlm.nih.gov/pubmed/10970688 http://dx.doi.org/10.1054/bjoc.2000.1404 |
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author | Krüger, W Lohner, R Jung, R Kröger, N Zander, A R |
author_facet | Krüger, W Lohner, R Jung, R Kröger, N Zander, A R |
author_sort | Krüger, W |
collection | PubMed |
description | Lineage-specific gene expression has been used for the identification of metastasis of cancers with unknown primary site or of disseminated cancer cells in haemopoietic compartments such as bone marrow or in lymph nodes. For the muc1, cytokeratin-19 and the CEA genes, the transcription in haemopoietic cells has been shown recently. Here, the expression of the mammary epithelium related antigens BA46 (lactadherin) and BA70 in lymphoid and myeloid cell lines, and in clinical specimens is analysed. By Northern-hybridization with specific oligonucleotides an ubiquitous transcription of both genes, independent from the provenance of cells or the chromosomal gender was found. Both mRNA molecules were amplified by rtPCR from the samples and the specificity could be confirmed by sequence analysis. Peptide-specific antibodies were raised in rabbits and used for Western-blot analysis and for immunocytochemical studies. Both antibodies reacted with total cell lysates from myeloid and lymphatic cells. In immunocytochemistry antibody P717 (anti-lactadherin) had a significant strong staining of the myeloid cell lines K562 and HL60 suggesting a participation of lactadherin in leukocyte-function. Using antibody P718, strong stains were seen in myeloid line K562 and lymphoid line ST486. In conclusion, our findings expand the results that the concept of lineage-specific gene expression is no longer valid at the molecular level. © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2374676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23746762009-09-10 Expression of human milk fat globulin proteins in cells of haemopoietic origin Krüger, W Lohner, R Jung, R Kröger, N Zander, A R Br J Cancer Regular Article Lineage-specific gene expression has been used for the identification of metastasis of cancers with unknown primary site or of disseminated cancer cells in haemopoietic compartments such as bone marrow or in lymph nodes. For the muc1, cytokeratin-19 and the CEA genes, the transcription in haemopoietic cells has been shown recently. Here, the expression of the mammary epithelium related antigens BA46 (lactadherin) and BA70 in lymphoid and myeloid cell lines, and in clinical specimens is analysed. By Northern-hybridization with specific oligonucleotides an ubiquitous transcription of both genes, independent from the provenance of cells or the chromosomal gender was found. Both mRNA molecules were amplified by rtPCR from the samples and the specificity could be confirmed by sequence analysis. Peptide-specific antibodies were raised in rabbits and used for Western-blot analysis and for immunocytochemical studies. Both antibodies reacted with total cell lysates from myeloid and lymphatic cells. In immunocytochemistry antibody P717 (anti-lactadherin) had a significant strong staining of the myeloid cell lines K562 and HL60 suggesting a participation of lactadherin in leukocyte-function. Using antibody P718, strong stains were seen in myeloid line K562 and lymphoid line ST486. In conclusion, our findings expand the results that the concept of lineage-specific gene expression is no longer valid at the molecular level. © 2000 Cancer Research Campaign Nature Publishing Group 2000-10 2000-09-04 /pmc/articles/PMC2374676/ /pubmed/10970688 http://dx.doi.org/10.1054/bjoc.2000.1404 Text en Copyright © 2000 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Regular Article Krüger, W Lohner, R Jung, R Kröger, N Zander, A R Expression of human milk fat globulin proteins in cells of haemopoietic origin |
title | Expression of human milk fat globulin proteins in cells of haemopoietic origin |
title_full | Expression of human milk fat globulin proteins in cells of haemopoietic origin |
title_fullStr | Expression of human milk fat globulin proteins in cells of haemopoietic origin |
title_full_unstemmed | Expression of human milk fat globulin proteins in cells of haemopoietic origin |
title_short | Expression of human milk fat globulin proteins in cells of haemopoietic origin |
title_sort | expression of human milk fat globulin proteins in cells of haemopoietic origin |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374676/ https://www.ncbi.nlm.nih.gov/pubmed/10970688 http://dx.doi.org/10.1054/bjoc.2000.1404 |
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