Genetic characteristics of the human hepatic stellate cell line LX-2.
The human hepatic cell line LX-2 has been described as tool to study mechanisms of hepatic fibrogenesis and the testing of antifibrotic compounds. It was originally generated by immortalisation with the Simian Vacuolating Virus 40 (SV40) transforming (T) antigen and subsequent propagation in low ser...
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doaj-13fb714e156d4946b886667d8d892c0f2020-11-25T00:48:22ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01810e7569210.1371/journal.pone.0075692Genetic characteristics of the human hepatic stellate cell line LX-2.Ralf WeiskirchenJörg WeimerSteffen K MeurerAnja KronBarbara SeipelInga VaterNorbert ArnoldReiner SiebertLieming XuScott L FriedmanCarsten BergmannThe human hepatic cell line LX-2 has been described as tool to study mechanisms of hepatic fibrogenesis and the testing of antifibrotic compounds. It was originally generated by immortalisation with the Simian Vacuolating Virus 40 (SV40) transforming (T) antigen and subsequent propagation in low serum conditions. Although this immortalized line is used in an increasing number of studies, detailed genetic characterisation has been lacking. We here have performed genetic characterisation of the LX-2 cell line and established a single-locus short tandem repeat (STR) profile for the cell line and characterized the LX-2 karyotype by several cytogenetic and molecular cytogenetic techniques. Spectral karyotyping (SKY) revealed a complex karyotype with a set of aberrations consistently present in the metaphases analyses which might serve as cytogenetic markers. In addition, various subclonal and single cell aberrations were detected. Our study provides criteria for genetic authentication of LX-2 and offers insights into the genotype changes which might underlie part of its phenotypic features.http://europepmc.org/articles/PMC3792989?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ralf Weiskirchen Jörg Weimer Steffen K Meurer Anja Kron Barbara Seipel Inga Vater Norbert Arnold Reiner Siebert Lieming Xu Scott L Friedman Carsten Bergmann |
spellingShingle |
Ralf Weiskirchen Jörg Weimer Steffen K Meurer Anja Kron Barbara Seipel Inga Vater Norbert Arnold Reiner Siebert Lieming Xu Scott L Friedman Carsten Bergmann Genetic characteristics of the human hepatic stellate cell line LX-2. PLoS ONE |
author_facet |
Ralf Weiskirchen Jörg Weimer Steffen K Meurer Anja Kron Barbara Seipel Inga Vater Norbert Arnold Reiner Siebert Lieming Xu Scott L Friedman Carsten Bergmann |
author_sort |
Ralf Weiskirchen |
title |
Genetic characteristics of the human hepatic stellate cell line LX-2. |
title_short |
Genetic characteristics of the human hepatic stellate cell line LX-2. |
title_full |
Genetic characteristics of the human hepatic stellate cell line LX-2. |
title_fullStr |
Genetic characteristics of the human hepatic stellate cell line LX-2. |
title_full_unstemmed |
Genetic characteristics of the human hepatic stellate cell line LX-2. |
title_sort |
genetic characteristics of the human hepatic stellate cell line lx-2. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
The human hepatic cell line LX-2 has been described as tool to study mechanisms of hepatic fibrogenesis and the testing of antifibrotic compounds. It was originally generated by immortalisation with the Simian Vacuolating Virus 40 (SV40) transforming (T) antigen and subsequent propagation in low serum conditions. Although this immortalized line is used in an increasing number of studies, detailed genetic characterisation has been lacking. We here have performed genetic characterisation of the LX-2 cell line and established a single-locus short tandem repeat (STR) profile for the cell line and characterized the LX-2 karyotype by several cytogenetic and molecular cytogenetic techniques. Spectral karyotyping (SKY) revealed a complex karyotype with a set of aberrations consistently present in the metaphases analyses which might serve as cytogenetic markers. In addition, various subclonal and single cell aberrations were detected. Our study provides criteria for genetic authentication of LX-2 and offers insights into the genotype changes which might underlie part of its phenotypic features. |
url |
http://europepmc.org/articles/PMC3792989?pdf=render |
work_keys_str_mv |
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