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...

Descripción completa

Detalles Bibliográficos
Autores principales: Gordon, Katrina E, Binas, Bert, Chapman, Rachel S, Kurian, Kathreena M, Clarkson, Richard W E, John Clark, A, Birgitte Lane, E, Watson, Christine J
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