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Physiological properties of astroglial cell lines derived from mice with high (SAMP8) and low (SAMR1, ICR) levels of endogenous retrovirus

Previous studies have reported that various inbred SAM mouse strains differ markedly with regard to a variety of parameters, such as capacity for learning and memory, life spans and brain histopathology. A potential cause of differences seen in these strains may be based on the fact that some strain...

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Autores principales: Kim, Boe-Hyun, Meeker, Harry C, Shin, Hae-Young, Kim, Jae-Il, Jeong, Byung-Hoon, Choi, Eun-Kyoung, Carp, Richard I, Kim, Yong-Sun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2607306/
https://www.ncbi.nlm.nih.gov/pubmed/19032740
http://dx.doi.org/10.1186/1742-4690-5-104
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author Kim, Boe-Hyun
Meeker, Harry C
Shin, Hae-Young
Kim, Jae-Il
Jeong, Byung-Hoon
Choi, Eun-Kyoung
Carp, Richard I
Kim, Yong-Sun
author_facet Kim, Boe-Hyun
Meeker, Harry C
Shin, Hae-Young
Kim, Jae-Il
Jeong, Byung-Hoon
Choi, Eun-Kyoung
Carp, Richard I
Kim, Yong-Sun
author_sort Kim, Boe-Hyun
collection PubMed
description Previous studies have reported that various inbred SAM mouse strains differ markedly with regard to a variety of parameters, such as capacity for learning and memory, life spans and brain histopathology. A potential cause of differences seen in these strains may be based on the fact that some strains have a high concentration of infectious murine leukemia virus (MuLV) in the brain, whereas other strains have little or no virus. To elucidate the effect of a higher titer of endogenous retrovirus in astroglial cells of the brain, we established astroglial cell lines from SAMR1 and SAMP8 mice, which are, respectively, resistant and prone to deficit in learning and memory and shortened life span. MuLV-negative astroglial cell lines established from ICR mice served as controls. Comparison of these cell lines showed differences in: 1) levels of the capsid antigen CAgag in both cell lysates and culture media, 2) expression of genomic retroelements, 3) the number of virus particles, 4) titer of infectious virus, 5) morphology, 6) replication rate of cells in culture and final cell concentrations, 7) expression pattern of proinflammatory cytokine genes. The results show that the expression of MuLV is much higher in SAMP8 than SAMR1 astrocyte cultures and that there are physiological differences in astroglia from the 2 strains. These results raise the possibility that the distinct physiological differences between SAMP8 and SAMR1 are a function of activation of endogenous retrovirus.
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spelling pubmed-26073062008-12-24 Physiological properties of astroglial cell lines derived from mice with high (SAMP8) and low (SAMR1, ICR) levels of endogenous retrovirus Kim, Boe-Hyun Meeker, Harry C Shin, Hae-Young Kim, Jae-Il Jeong, Byung-Hoon Choi, Eun-Kyoung Carp, Richard I Kim, Yong-Sun Retrovirology Research Previous studies have reported that various inbred SAM mouse strains differ markedly with regard to a variety of parameters, such as capacity for learning and memory, life spans and brain histopathology. A potential cause of differences seen in these strains may be based on the fact that some strains have a high concentration of infectious murine leukemia virus (MuLV) in the brain, whereas other strains have little or no virus. To elucidate the effect of a higher titer of endogenous retrovirus in astroglial cells of the brain, we established astroglial cell lines from SAMR1 and SAMP8 mice, which are, respectively, resistant and prone to deficit in learning and memory and shortened life span. MuLV-negative astroglial cell lines established from ICR mice served as controls. Comparison of these cell lines showed differences in: 1) levels of the capsid antigen CAgag in both cell lysates and culture media, 2) expression of genomic retroelements, 3) the number of virus particles, 4) titer of infectious virus, 5) morphology, 6) replication rate of cells in culture and final cell concentrations, 7) expression pattern of proinflammatory cytokine genes. The results show that the expression of MuLV is much higher in SAMP8 than SAMR1 astrocyte cultures and that there are physiological differences in astroglia from the 2 strains. These results raise the possibility that the distinct physiological differences between SAMP8 and SAMR1 are a function of activation of endogenous retrovirus. BioMed Central 2008-11-25 /pmc/articles/PMC2607306/ /pubmed/19032740 http://dx.doi.org/10.1186/1742-4690-5-104 Text en Copyright © 2008 Kim et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kim, Boe-Hyun
Meeker, Harry C
Shin, Hae-Young
Kim, Jae-Il
Jeong, Byung-Hoon
Choi, Eun-Kyoung
Carp, Richard I
Kim, Yong-Sun
Physiological properties of astroglial cell lines derived from mice with high (SAMP8) and low (SAMR1, ICR) levels of endogenous retrovirus
title Physiological properties of astroglial cell lines derived from mice with high (SAMP8) and low (SAMR1, ICR) levels of endogenous retrovirus
title_full Physiological properties of astroglial cell lines derived from mice with high (SAMP8) and low (SAMR1, ICR) levels of endogenous retrovirus
title_fullStr Physiological properties of astroglial cell lines derived from mice with high (SAMP8) and low (SAMR1, ICR) levels of endogenous retrovirus
title_full_unstemmed Physiological properties of astroglial cell lines derived from mice with high (SAMP8) and low (SAMR1, ICR) levels of endogenous retrovirus
title_short Physiological properties of astroglial cell lines derived from mice with high (SAMP8) and low (SAMR1, ICR) levels of endogenous retrovirus
title_sort physiological properties of astroglial cell lines derived from mice with high (samp8) and low (samr1, icr) levels of endogenous retrovirus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2607306/
https://www.ncbi.nlm.nih.gov/pubmed/19032740
http://dx.doi.org/10.1186/1742-4690-5-104
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