Extrahepatic expression of apolipoprotein A-II in mouse tissues: Possible contribution to mouse senile amyloidosis

被引:14
作者
Fu, L
Matsuyama, I
Chiba, T
Xing, YM
Korenaga, T
Guo, ZJ
Fu, XY
Nakayama, J
Mori, M
Higuchi, K [1 ]
机构
[1] Shinshu Univ, Sch Med, Dept Aging Angiol, Res Ctr Aging & Adaptat, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Sch Med, Dept Lab Med, Matsumoto, Nagano 3908621, Japan
[3] Nagano Canc Detect Ctr, Div Clin Pathol, Matsumoto, Nagano, Japan
关键词
amyloidosis; mouse; apoA-II mRNA; in situ hybridization;
D O I
10.1177/002215540104900607
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Apolipoprotein A-II (apoA-II), an apolipoprotein in serum high-density lipoprotein, is a precursor of mouse senile amyloid fibrils. The liver has been considered to be the primary site of synthesis. However, we performed nonradioactive in situ hybridization analysis in tissue sections from young and old amyloidogenic (R1.P1-Apoa2(C)) and amyloid-resistant (SAMR1) mice and revealed that other tissues in addition to the liver synthesize apoA-II. We found a strong hybridization signal in the basal cells of the squamous epithelium and the chief cells of the fundic gland in the stomach, the crypt cells and a small portion of the absorptive epithelial cells in the small intestine, the basal cells of the tongue mucosa, and the basal cells of the epidermis and hair follicles in the skin in both mouse strains. Expression of apoA-II mRNA in those tissues was also examined by RT-PCR analysis. Immunolocalization of apoA-II protein also indicated the cellular localization of apoA-II. ApoA-II transcription was not observed in the heart. Amyloid deposition was observed around the cells expressing apoA-II mRNA in the old R1.P1-Apoa2(C) mice. These results demonstrate that the apoA-II mRNA is transcribed and translated in various extrahepatic tissues and suggest a possible contribution of apoA-II synthesized in these tissues to amyloid deposition.
引用
收藏
页码:739 / 747
页数:9
相关论文
共 43 条
[1]  
AKERLOF E, 1991, BIOCHEMISTRY-US, V30, P8986
[2]  
BLACKBURN WD, 1991, J LIPID RES, V32, P1911
[3]   Mouse senile amyloid deposition is suppressed by adenovirus-mediated overexpression of amyloid-resistant apolipoprotein A-II [J].
Chiba, T ;
Kogishi, K ;
Wang, J ;
Xia, C ;
Matsushita, T ;
Miyazaki, J ;
Saito, I ;
Hosokawa, M ;
Higuchi, K .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (04) :1319-1326
[4]  
EGGERMAN TL, 1991, J LIPID RES, V32, P821
[5]  
HAMILTON KK, 1993, J BIOL CHEM, V268, P3632
[6]   APOLIPOPROTEINS AI, AII, AND CI STIMULATE PLACENTAL-LACTOGEN RELEASE FROM HUMAN PLACENTAL TISSUE - A NOVEL ACTION OF HIGH-DENSITY-LIPOPROTEIN APOLIPOPROTEINS [J].
HANDWERGER, S ;
QUARFORDT, S ;
BARRETT, J ;
HARMAN, I .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (02) :625-628
[7]  
HIGUCHI K, 1983, LAB INVEST, V48, P231
[8]   DEVELOPMENT OF CONGENIC STRAINS OF MICE CARRYING AMYLOIDOGENIC APOLIPOPROTEIN A-II (APOA2(C)) - APOA2(C) REDUCES THE PLASMA-LEVEL AND THE SIZE OF HIGH-DENSITY-LIPOPROTEIN [J].
HIGUCHI, K ;
KITADO, H ;
KITAGAWA, K ;
KOGISHI, K ;
NAIKI, H ;
TAKEDA, T .
FEBS LETTERS, 1993, 317 (03) :207-210
[9]   POLYMORPHISM OF APOLIPOPROTEIN-A-II (APOA-II) AMONG INBRED STRAINS OF MICE - RELATIONSHIP BETWEEN THE MOLECULAR TYPE OF APOA-II AND MOUSE SENILE AMYLOIDOSIS [J].
HIGUCHI, K ;
KITAGAWA, K ;
NAIKI, H ;
HANADA, K ;
HOSOKAWA, M ;
TAKEDA, T .
BIOCHEMICAL JOURNAL, 1991, 279 :427-433
[10]  
HIGUCHI K, 1995, LAB INVEST, V72, P75