Generation of APLP2 KO mice and early postnatal lethality in APLP2/APP double KO mice

被引:280
作者
Von Koch, CS
Zheng, H
Chen, H
Trumbauer, M
Thinakaran, G
Van der Ploeg, LHT
Price, DL
Sisodia, SS
机构
[1] Johns Hopkins Univ, Sch Med, Neuropathol Lab, Dept Neurosci, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Div Neuropathol, Baltimore, MD 21205 USA
[4] Merck & Co Inc, Merck Sharp & Dohme Res Labs, Rahway, NJ 07065 USA
关键词
amyloid precursor protein; amyloid precursor-like protein; gene targeting; axonal outgrowth; olfactory epithelium;
D O I
10.1016/S0197-4580(97)00151-6
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Amyloid precursor protein (APP) is a member of a larger gene family including amyloid precursor-like proteins (APLP), APLP2 and APLP1. To examine the function of APLP2 in vivo, we generated APLP2 knockout (KO) mice. They are of normal size, fertile, and appear healthy up to 22 months of age. We observed no impaired axonal outgrowth of olfactory sensory neurons following bulbectomy, suggesting against an important role for APLP2 alone in this process. Because APLP2 and APP are highly homologous and may serve similar functions in vivo, we generated mice with targeted APLP2 and APP alleles. Approximately 80% of double KO mice die within the first week after birth, suggesting that APLP2 and APP are required for early postnatal development. The surviving similar to 20% of double KO mice are 20-30% reduced in weight and show difficulty in righting, ataxia, spinning behavior, and a head tilt, suggesting a deficit in balance and/or strength. Adult double KO mice mate poorly, despite apparent normal ovarian and testicular development. Otherwise, double KO mice appear healthy up to 13 months of age. We conclude, that APLP2 and APP can substitute for each other functionally. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:661 / 669
页数:9
相关论文
共 42 条
[1]  
Bradley A., 1987, TERATOCARCINOMAS EMB, P113
[2]   BETA-AMYLOID PRECURSOR PROTEIN MEDIATES NEURONAL CELL-CELL AND CELL-SURFACE ADHESION [J].
BREEN, KC ;
BRUCE, M ;
ANDERTON, BH .
JOURNAL OF NEUROSCIENCE RESEARCH, 1991, 28 (01) :90-100
[3]   CHONDROITIN SULFATE AS A REGULATOR OF NEURONAL PATTERNING IN THE RETINA [J].
BRITTIS, PA ;
CANNING, DR ;
SILVER, J .
SCIENCE, 1992, 255 (5045) :733-736
[4]   AN ANTIBODY TO BETA-AMYLOID AND THE AMYLOID PRECURSOR PROTEIN INHIBITS CELL-SUBSTRATUM ADHESION IN MANY MAMMALIAN-CELL TYPES [J].
CHEN, M ;
YANKNER, BA .
NEUROSCIENCE LETTERS, 1991, 125 (02) :223-226
[5]   EXPRESSION OF THE AMYLOID PROTEIN-PRECURSOR OF ALZHEIMERS-DISEASE IN THE DEVELOPING RAT OLFACTORY SYSTEM [J].
CLARRIS, HJ ;
KEY, B ;
BEYREUTHER, K ;
MASTERS, CL ;
SMALL, DH .
DEVELOPMENTAL BRAIN RESEARCH, 1995, 88 (01) :87-95
[6]   Activation of K+ channels and suppression of neuronal activity by secreted beta-amyloid-precursor protein [J].
Furukawa, K ;
Barger, SW ;
Blalock, EM ;
Mattson, MP .
NATURE, 1996, 379 (6560) :74-78
[7]   ALZHEIMERS-DISEASE - INITIAL REPORT OF THE PURIFICATION AND CHARACTERIZATION OF A NOVEL CEREBROVASCULAR AMYLOID PROTEIN [J].
GLENNER, GG ;
WONG, CW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 120 (03) :885-890
[8]   THE COMPLETE CDNA CODING SEQUENCE FOR THE MOUSE CDEI BINDING-PROTEIN [J].
HANES, J ;
VONDERKAMMER, H ;
KRISTJANSSON, GI ;
SCHEIT, KH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1216 (01) :154-156
[9]   GLYCOSAMINOGLYCANS - MOLECULAR-PROPERTIES, PROTEIN INTERACTIONS, AND ROLE IN PHYSIOLOGICAL PROCESSES [J].
JACKSON, RL ;
BUSCH, SJ ;
CARDIN, AD .
PHYSIOLOGICAL REVIEWS, 1991, 71 (02) :481-539
[10]   AMYLOID BETA-PROTEIN PRECURSOR IS ASSOCIATED WITH EXTRACELLULAR-MATRIX [J].
KLIER, FG ;
COLE, G ;
STALLCUP, W ;
SCHUBERT, D .
BRAIN RESEARCH, 1990, 515 (1-2) :336-342