Cargando…
A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland
BACKGROUND: This paper describes the derivation and characterization of a novel, conditionally immortal mammary epithelial cell line named KIM-2. These cells were derived from mid-pregnant mammary glands of a mouse harbouring one to two copies of a transgene comprised of the ovine β-lactoglobulin mi...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2000
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13917/ https://www.ncbi.nlm.nih.gov/pubmed/11056687 |
_version_ | 1782119850337894400 |
---|---|
author | Gordon, Katrina E Binas, Bert Chapman, Rachel S Kurian, Kathreena M Clarkson, Richard W E John Clark, A Birgitte Lane, E Watson, Christine J |
author_facet | Gordon, Katrina E Binas, Bert Chapman, Rachel S Kurian, Kathreena M Clarkson, Richard W E John Clark, A Birgitte Lane, E Watson, Christine J |
author_sort | Gordon, Katrina E |
collection | PubMed |
description | BACKGROUND: This paper describes the derivation and characterization of a novel, conditionally immortal mammary epithelial cell line named KIM-2. These cells were derived from mid-pregnant mammary glands of a mouse harbouring one to two copies of a transgene comprised of the ovine β-lactoglobulin milk protein gene promoter, driving expression of a temperature-sensitive variant of simian virus-40 (SV40) large T antigen (T-Ag). RESULTS: KIM-2 cells have a characteristic luminal epithelial cell morphology and a stable, nontransformed phenotype at the semipermissive temperature of 37°C. In contrast, at the permissive temperature of 33°C the cells have an elongated spindle-like morphology and become transformed after prolonged culture. Differentiation of KIM-2 cells at 37°C, in response to lactogenic hormones, results in the formation of polarized dome-like structures with tight junctions. This is accompanied by expression of the milk protein genes that encode β-casein and whey acidic protein (WAP), and activation of the prolactin signalling molecule, signal transducer and activator of transcription (STAT)5. Fully differentiated KIM-2 cultures at 37°C become dependent on lactogenic hormones for survival and undergo extensive apoptosis upon hormone withdrawal, as indicated by nuclear morphology and flow cytometric analysis. KIM-2 cells can be genetically modified by stable transfection and clonal lines isolated that retain the characteristics of untransfected cells. CONCLUSION: KIM-2 cells are a valuable addition, therefore, to currently available lines of mammary epithelial cells. Their capacity for extensive differentiation in the absence of exogenously added basement membrane, and ability to undergo apoptosis in response to physiological signals will provide an invaluable model system for the study of signal transduction pathways and transcriptional regulatory mechanisms that control differentiation and involution in the mammary gland. |
format | Text |
id | pubmed-13917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-139172001-02-27 A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland Gordon, Katrina E Binas, Bert Chapman, Rachel S Kurian, Kathreena M Clarkson, Richard W E John Clark, A Birgitte Lane, E Watson, Christine J Breast Cancer Res Primary Research BACKGROUND: This paper describes the derivation and characterization of a novel, conditionally immortal mammary epithelial cell line named KIM-2. These cells were derived from mid-pregnant mammary glands of a mouse harbouring one to two copies of a transgene comprised of the ovine β-lactoglobulin milk protein gene promoter, driving expression of a temperature-sensitive variant of simian virus-40 (SV40) large T antigen (T-Ag). RESULTS: KIM-2 cells have a characteristic luminal epithelial cell morphology and a stable, nontransformed phenotype at the semipermissive temperature of 37°C. In contrast, at the permissive temperature of 33°C the cells have an elongated spindle-like morphology and become transformed after prolonged culture. Differentiation of KIM-2 cells at 37°C, in response to lactogenic hormones, results in the formation of polarized dome-like structures with tight junctions. This is accompanied by expression of the milk protein genes that encode β-casein and whey acidic protein (WAP), and activation of the prolactin signalling molecule, signal transducer and activator of transcription (STAT)5. Fully differentiated KIM-2 cultures at 37°C become dependent on lactogenic hormones for survival and undergo extensive apoptosis upon hormone withdrawal, as indicated by nuclear morphology and flow cytometric analysis. KIM-2 cells can be genetically modified by stable transfection and clonal lines isolated that retain the characteristics of untransfected cells. CONCLUSION: KIM-2 cells are a valuable addition, therefore, to currently available lines of mammary epithelial cells. Their capacity for extensive differentiation in the absence of exogenously added basement membrane, and ability to undergo apoptosis in response to physiological signals will provide an invaluable model system for the study of signal transduction pathways and transcriptional regulatory mechanisms that control differentiation and involution in the mammary gland. BioMed Central 2000 2000-03-07 /pmc/articles/PMC13917/ /pubmed/11056687 Text en Copyright © 2000 Current Science Ltd |
spellingShingle | Primary Research Gordon, Katrina E Binas, Bert Chapman, Rachel S Kurian, Kathreena M Clarkson, Richard W E John Clark, A Birgitte Lane, E Watson, Christine J A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland |
title | A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland |
title_full | A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland |
title_fullStr | A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland |
title_full_unstemmed | A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland |
title_short | A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland |
title_sort | novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13917/ https://www.ncbi.nlm.nih.gov/pubmed/11056687 |
work_keys_str_mv | AT gordonkatrinae anovelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT binasbert anovelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT chapmanrachels anovelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT kuriankathreenam anovelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT clarksonrichardwe anovelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT johnclarka anovelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT birgittelanee anovelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT watsonchristinej anovelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT gordonkatrinae novelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT binasbert novelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT chapmanrachels novelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT kuriankathreenam novelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT clarksonrichardwe novelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT johnclarka novelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT birgittelanee novelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland AT watsonchristinej novelcellculturemodelforstudyingdifferentiationandapoptosisinthemousemammarygland |