Murine leukemia virus in organs of senescence-prone and -resistant mouse strains

被引:17
作者
Carp, RI
Meeker, HC
Chung, R
Kozak, CA
Hosokawa, M
Fujisawa, H
机构
[1] New York State Inst Basic Res Dev Disabil, Staten Isl, NY 10314 USA
[2] NIH, Bethesda, MD 20892 USA
[3] Kyoto Univ, Inst Frontier Med Sci, Field Regenerat Control, Kyoto 6068507, Japan
关键词
murine leukemia virus; accelerated senescence; mouse strain;
D O I
10.1016/S0047-6374(01)00377-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A series of inbred strains of mice have been developed that are either prone (SAMP) or resistant (SAMR) to accelerated senescence. All of these strains originated from an inadvertent cross or crosses between the AKR/J mouse strain and an unknown strain(s). The characteristics of the nine senescence-prone lines differ, with all strains showing generalized aspects of accelerated aging but with each line having a specific aging-related change that is emphasized, e.g. learning and memory deficits, osteoporosis and senile amyloidosis. The senescence-resistant strains have normal patterns of aging and do not show the specific aging-related changes seen in SAMP strains. The fact that AKR mice have high levels of endogenous, ecotropic murine leukemia virus (MuLV) prompted an examination of the expression levels of MuLV in SAM strains. Analysis of brain, spleen and thymus samples revealed that seven of nine SAMP strains had high levels of MuLV and contained the Emv11 provirus, (previously termed Akv1) that encodes the predominant MuLV found in AKR mice. In contrast, none of the SAMR strains had Emv11 or significant amounts of virus. The current findings represent an initial step in determining the role of MuLV in the accelerated senescence seen in SAMP strains. Published by Elsevier Science Ireland Ltd.
引用
收藏
页码:575 / 584
页数:10
相关论文
共 26 条
[1]   VARIATION IN THE NUMBER OF COPIES AND IN THE GENOMIC ORGANIZATION OF ECOTROPIC MURINE LEUKEMIA-VIRUS PROVIRAL SEQUENCES IN SUBLINES OF AKR MICE [J].
BUCKLER, CE ;
STAAL, SP ;
ROWE, WP ;
MARTIN, MA .
JOURNAL OF VIROLOGY, 1982, 43 (02) :629-640
[2]   Analysis of the incubation periods, induction of obesity and histopathological changes in senescence-prone and senescence-resistant mice infected with various scrapie strains [J].
Carp, RI ;
Meeker, H ;
Sersen, E ;
Kozlowski, P .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :2863-2869
[3]   Scrapie strain-specific interactions with endogenous murine leukaemia virus [J].
Carp, RI ;
Meeker, HC ;
Caruso, V ;
Sersen, E .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :5-10
[4]   IDENTIFICATION OF ECOTROPIC PROVIRAL SEQUENCES IN INBRED MOUSE STRAINS WITH A CLONED SUBGENOMIC DNA FRAGMENT [J].
CHAN, HW ;
BRYAN, T ;
MOORE, JL ;
STAAL, SP ;
ROWE, WP ;
MARTIN, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (10) :5779-5783
[5]   AGE-RELATED-CHANGES IN FOOTSHOCK AVOIDANCE ACQUISITION AND RETENTION IN SENESCENCE ACCELERATED MOUSE (SAM) [J].
FLOOD, JF ;
MORLEY, JE .
NEUROBIOLOGY OF AGING, 1993, 14 (02) :153-157
[6]   AGE-RELATED-CHANGES IN LEARNING, MEMORY, AND LIPOFUSCIN AS A FUNCTION OF THE PERCENTAGE OF SAMP8 GENES [J].
FLOOD, JF ;
MORLEY, PMK ;
MORLEY, JE .
PHYSIOLOGY & BEHAVIOR, 1995, 58 (04) :819-822
[7]   EARLY ONSET OF AGE-RELATED IMPAIRMENT OF AVERSIVE AND APPETITIVE LEARNING IN THE SAM-P/8 MOUSE [J].
FLOOD, JF ;
MORLEY, JE .
JOURNALS OF GERONTOLOGY, 1992, 47 (02) :B52-B59
[8]   Increased mitochondrial DNA deletion in the brain of SAMP8, a mouse model for spontaneous oxidative stress brain [J].
Fujibayashi, Y ;
Yamamoto, S ;
Waki, A ;
Konishi, J ;
Yonekura, Y .
NEUROSCIENCE LETTERS, 1998, 254 (02) :109-112
[9]   LEVEL AND SHAPE OF SEQUENCES OF MOTOR BEHAVIOR IN INBRED AND HYBRID MICE [J].
GUTTMAN, R ;
LIEBLICH, I ;
FRANKEL, E .
BEHAVIOR GENETICS, 1980, 10 (03) :251-261
[10]  
HABU H, 1994, INT CONGR SER, V1062, P343