Role of the low-density lipoprotein receptor-related protein in β-amyloid metabolism and Alzheimer disease

被引:92
作者
Hyman, BT
Strickland, D
Rebeck, GW
机构
[1] Massachusetts Gen Hosp, Alzheimer Dis Res Lab, Boston, MA 02129 USA
[2] Amer Red Cross, Holland Lab, Rockville, MD USA
关键词
D O I
10.1001/archneur.57.5.646
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Deposition of beta-amyloid (A beta), a metabolite of approximately 4 kd of the amyloid precursor protein, is a critical pathological feature in Alzheimer disease. We postulate that deposition reflects an imbalance of A beta synthesis and clearance. Several pathways that impact A beta converge on a single receptor molecule, the low-density lipoprotein receptor-related protein (LRP). This multifunctional receptor is the major neuronal receptor both for apolipoprotein E (apoE, protein; APOE, gene) and for alpha(2)-macroglobulin (alpha(2)M, protein, A2M, gene), and it mediates clearance of apoE/A beta and alpha(2)M/A beta complexes. The LRP also interacts with the amyloid precursor protein itself. In this review, we highlight data that support a role for LRP in A beta metabolism and hypothesize that LRP therefore plays a critical role in Alzheimer disease.
引用
收藏
页码:646 / 650
页数:5
相关论文
共 85 条
[21]  
HERZ J, 1991, J BIOL CHEM, V266, P21232
[22]   Confirmation of an association between a polymorphism in exon 3 of the low-density lipoprotein receptor-related protein gene and Alzheimer's disease [J].
Hollenbach, E ;
Ackermann, S ;
Hyman, BT ;
Rebeck, GW .
NEUROLOGY, 1998, 50 (06) :1905-1907
[23]  
Hollister RD, 1996, BRAIN RES, V728, P13
[24]   LOW-DENSITY-LIPOPROTEIN RECEPTOR-RELATED PROTEIN MEDIATES APOLIPOPROTEIN E-DEPENDENT NEURITE OUTGROWTH IN A CENTRAL NERVOUS SYSTEM-DERIVED NEURONAL CELL-LINE [J].
HOLTZMAN, DM ;
PITAS, RE ;
KILBRIDGE, J ;
NATHAN, B ;
MAHLEY, RW ;
BU, GJ ;
SCHWARTZ, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (21) :9480-9484
[25]  
Howell BW, 1999, MOL CELL BIOL, V19, P5179
[26]   α2-macroglobulin associates with β-amyloid peptide and prevents fibril formation [J].
Hughes, SR ;
Khorkova, O ;
Goyal, S ;
Knaeblein, J ;
Heroux, J ;
Riedel, NG ;
Sahasrabudhe, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :3275-3280
[27]  
Hyman BT, 1996, J AM GERIATR SOC, V44, P1469, DOI 10.1111/j.1532-5415.1996.tb04073.x
[28]   THE LACK OF ACCUMULATION OF SENILE PLAQUES OR AMYLOID BURDEN IN ALZHEIMERS-DISEASE SUGGESTS A DYNAMIC BALANCE BETWEEN AMYLOID DEPOSITION AND RESOLUTION [J].
HYMAN, BT ;
MARZLOFF, K ;
ARRIAGADA, PV .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1993, 52 (06) :594-600
[29]   SEEDING ONE-DIMENSIONAL CRYSTALLIZATION OF AMYLOID - A PATHOGENIC MECHANISM IN ALZHEIMERS-DISEASE AND SCRAPIE [J].
JARRETT, JT ;
LANSBURY, PT .
CELL, 1993, 73 (06) :1055-1058
[30]  
Jordán J, 1998, J NEUROSCI, V18, P195