Reelin Is a Ligand for Lipoprotein Receptors

A signaling pathway involving the extracellular protein Reelin and the intracellular adaptor protein Disabled-1 (Dab1) controls cell positioning during mammalian brain development. Here, we demonstrate that Reelin binds directly to lipoprotein receptors, preferably the very low-density lipoprotein receptor (VLDLR) and apolipoprotein E receptor 2 (ApoER2). Binding requires calcium, and it is inhibited in the presence of apoE. Furthermore, the CR-50 monoclonal antibody, which inhibits Reelin function, blocks the association of Reelin with VLDLR. After binding to VLDLR on the cell surface, Reelin is internalized into vesicles. In dissociated neurons, apoE reduces the level of Reelin-induced tyrosine phosphorylation of Dab1. These data suggest that Reelin directs neuronal migration by binding to VLDLR and ApoER2.

[1]  W. Strittmatter,et al.  Apolipoprotein E Binds to and Potentiates the Biological Activity of Ciliary Neurotrophic Factor , 1997, The Journal of Neuroscience.

[2]  Jonathan A. Cooper,et al.  Neuronal position in the developing brain is regulated by mouse disabled-1 , 1997, Nature.

[3]  E. Shooter,et al.  Denervated sheath cells secrete a new protein after nerve injury. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[4]  A D Roses,et al.  Apolipoprotein E and Alzheimer disease. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[5]  T. Curran,et al.  Disabled-1 acts downstream of Reelin in a signaling pathway that controls laminar organization in the mammalian brain. , 1998, Development.

[6]  T. Südhof,et al.  First cysteine-rich repeat in ligand-binding domain of low density lipoprotein receptor binds Ca2+ and monoclonal antibodies, but not lipoproteins. , 1987, The Journal of biological chemistry.

[7]  L. Tsai,et al.  Mice Lacking p35, a Neuronal Specific Activator of Cdk5, Display Cortical Lamination Defects, Seizures, and Adult Lethality , 1997, Neuron.

[8]  R. Mahley,et al.  Abnormal lipoprotein receptor-binding activity of the human E apoprotein due to cysteine-arginine interchange at a single site. , 1982, The Journal of biological chemistry.

[9]  R. Hammer,et al.  RAP, a specialized chaperone, prevents ligand‐induced ER retention and degradation of LDL receptor‐related endocytic receptors. , 1996, The EMBO journal.

[10]  M. Frotscher,et al.  A role for Cajal–Retzius cells and reelin in the development of hippocampal connections , 1997, Nature.

[11]  W. Schneider,et al.  The VLDL receptor: an LDL receptor relative with eight ligand binding repeats, LR8. , 1998, Atherosclerosis.

[12]  A. Goffinet,et al.  The reeler mouse as a model of brain development. , 1998, Advances in anatomy, embryology, and cell biology.

[13]  R. Mahley,et al.  Binding of arginine-rich (E) apoprotein after recombination with phospholipid vesicles to the low density lipoprotein receptors of fibroblasts. , 1979, The Journal of biological chemistry.

[14]  A. Goffinet,et al.  Reelin, the Extracellular Matrix Protein Deficient in Reeler Mutant Mice, Is Processed by a Metalloproteinase , 1999, Experimental Neurology.

[15]  T. Curran,et al.  Reeler: new tales on an old mutant mouse , 1998, BioEssays : news and reviews in molecular, cellular and developmental biology.

[16]  K. Mikoshiba,et al.  Reelin Regulates the Development and Synaptogenesis of the Layer-Specific Entorhino-Hippocampal Connections , 1999, The Journal of Neuroscience.

[17]  W. Schneider Yolk precursor transport in the laying hen , 1995, Current opinion in lipidology.

[18]  W. Schneider,et al.  Avian and murine LR8B and human apolipoprotein E receptor 2: differentially spliced products from corresponding genes. , 1997, Genomics.

[19]  M. Seike,et al.  The reeler gene-associated antigen on cajal-retzius neurons is a crucial molecule for laminar organization of cortical neurons , 1995, Neuron.

[20]  C. Finch,et al.  Astrocytic apolipoprotein E mRNA and GFAP mRNA in hippocampus after entorhinal cortex lesioning. , 1991, Brain research. Molecular brain research.

[21]  Jonathan A. Cooper,et al.  Reelin-induced tryosine phosphorylation of Disabled 1 during neuronal positioning , 1999 .

[22]  Deborah Fass,et al.  Molecular basis of familial hypercholesterolaemia from structure of LDL receptor module , 1997, Nature.

[23]  T. Terashima,et al.  Expression of reelin, the gene responsible for the reeler mutation, in embryonic development and adulthood in the mouse , 1997, Developmental dynamics : an official publication of the American Association of Anatomists.

[24]  J. Borg,et al.  Interaction of Cytosolic Adaptor Proteins with Neuronal Apolipoprotein E Receptors and the Amyloid Precursor Protein* , 1998, The Journal of Biological Chemistry.

[25]  D. Strickland,et al.  The 39-kDa receptor-associated protein regulates ligand binding by the very low density lipoprotein receptor. , 1994, The Journal of biological chemistry.

[26]  K. Imahori,et al.  Physiology and pathology of tau protein kinases in relation to Alzheimer's disease. , 1997, Journal of biochemistry.

[27]  D. Russell,et al.  Different combinations of cysteine-rich repeats mediate binding of low density lipoprotein receptor to two different proteins. , 1989, The Journal of biological chemistry.

[28]  Y. Kawarabayasi,et al.  Expression and characterization of a very low density lipoprotein receptor variant lacking the O-linked sugar region generated by alternative splicing. , 1998, Journal of biochemistry.

[29]  K. Mikoshiba,et al.  Disruption of hippocampal development in vivo by CR-50 mAb against reelin. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[30]  C. Sotelo,et al.  Regional and Cellular Patterns of reelin mRNA Expression in the Forebrain of the Developing and Adult Mouse , 1998, The Journal of Neuroscience.

[31]  Ramin Homayouni,et al.  Disabled-1 Binds to the Cytoplasmic Domain of Amyloid Precursor-Like Protein 1 , 1999, The Journal of Neuroscience.

[32]  M. S. Brown,et al.  Normal plasma lipoproteins and fertility in gene-targeted mice homozygous for a disruption in the gene encoding very low density lipoprotein receptor. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[33]  Y. Kawarabayasi,et al.  Rabbit very low density lipoprotein receptor: a low density lipoprotein receptor-like protein with distinct ligand specificity. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[34]  R. Mahley,et al.  Apolipoprotein E: cholesterol transport protein with expanding role in cell biology. , 1988, Science.

[35]  K. Goto,et al.  Human Apolipoprotein E Receptor 2 , 1996, The Journal of Biological Chemistry.

[36]  Jonathan A. Cooper,et al.  Mouse disabled (mDab1): a Src binding protein implicated in neuronal development , 1997, The EMBO journal.

[37]  D. Price,et al.  Mutant genes in familial Alzheimer's disease and transgenic models. , 1998, Annual review of neuroscience.

[38]  John Shelton,et al.  Reeler/Disabled-like Disruption of Neuronal Migration in Knockout Mice Lacking the VLDL Receptor and ApoE Receptor 2 , 1999, Cell.

[39]  J. Gliemann,et al.  Receptors of the low density lipoprotein (LDL) receptor family in man. Multiple functions of the large family members via interaction with complex ligands. , 1998, Biological chemistry.

[40]  T. Curran,et al.  A protein related to extracellular matrix proteins deleted in the mouse mutant reeler , 1995, Nature.

[41]  M. Brown,et al.  NPXY, a sequence often found in cytoplasmic tails, is required for coated pit-mediated internalization of the low density lipoprotein receptor. , 1990, The Journal of biological chemistry.

[42]  Dan Goldowitz,et al.  Scrambler and yotari disrupt the disabled gene and produce a reeler -like phenotype in mice , 1997, Nature.

[43]  Veeranna,et al.  Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[44]  A. Goffinet,et al.  A panel of monoclonal antibodies against reelin, the extracellular matrix protein defective in reeler mutant mice , 1998, Journal of Neuroscience Methods.

[45]  T. Willnow Receptor-associated protein (RAP): a specialized chaperone for endocytic receptors. , 1998, Biological chemistry.

[46]  A. Goffinet,et al.  Brain Development in Normal and reeler Mice: the Phenotype , 1998 .

[47]  Jonathan A. Cooper,et al.  Phospholipids of Transmembrane Glycoproteins and to Domain Binds to the Internalization Signals The Disabled 1 Phosphotyrosine-Binding , 1999 .

[48]  K. Mikoshiba,et al.  Regulation of Purkinje Cell Alignment by Reelin as Revealed with CR-50 Antibody , 1997, The Journal of Neuroscience.

[49]  M. Brown,et al.  A receptor-mediated pathway for cholesterol homeostasis. , 1986, Science.

[50]  K. Mikoshiba,et al.  Reelin Is a Secreted Glycoprotein Recognized by the CR-50 Monoclonal Antibody , 1997, The Journal of Neuroscience.