Signalling: γ-Secretase-mediated proteolysis in cell-surface-receptor signalling

Many cell-surface receptors transmit signals to the nucleus through complex protein cascades. By contrast, the Notch signalling pathway uses a relatively direct mechanism, in which the intracellular domain of the receptor is liberated by intramembrane cleavage and translocates to the nucleus. This critical cleavage is mediated by the γ-secretase complex, and new findings reveal that this mechanism is used by various receptors, although many questions remain about the biochemical details.

[1]  P. Rather,et al.  Providencia stuartii Genes Activated by Cell-to-Cell Signaling and Identification of a Gene Required for Production or Activity of an Extracellular Factor , 1999, Journal of bacteriology.

[2]  Iva Greenwald,et al.  Facilitation of lin-12-mediated signalling by sel-12, a Caenorhabditis elegans S182 Alzheimer's disease gene , 1995, Nature.

[3]  I. Greenwald,et al.  Effects of SEL-12 presenilin on LIN-12 localization and function in Caenorhabditis elegans. , 1998, Development.

[4]  A. Goate,et al.  A common enzyme connects notch signaling and Alzheimer's disease. , 2000, Genes & development.

[5]  S. Campuzano,et al.  The metalloprotease-disintegrin Kuzbanian participates in Notch activation during growth and patterning of Drosophila imaginal discs. , 1997, Development.

[6]  M. Diamond Facts and fiction. , 1994, Journal of the American Dental Association.

[7]  M. Freeman,et al.  Drosophila Rhomboid-1 Defines a Family of Putative Intramembrane Serine Proteases , 2001, Cell.

[8]  A. Bernstein,et al.  Mice lacking both presenilin genes exhibit early embryonic patterning defects. , 1999, Genes & development.

[9]  E. Parker,et al.  PS1 N- and C-terminal fragments form a complex that functions in APP processing and Notch signaling , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[10]  D. Selkoe,et al.  Translating cell biology into therapeutic advances in Alzheimer's disease , 1999, Nature.

[11]  S. Artavanis-Tsakonas,et al.  Nucleotide sequence from the neurogenic locus Notch implies a gene product that shares homology with proteins containing EGF-like repeats , 1985, Cell.

[12]  S. Artavanis-Tsakonas,et al.  Comparative aspects of Notch signaling in lower and higher eukaryotes. , 1997, Perspectives on developmental neurobiology.

[13]  P. S. St George-Hyslop,et al.  Mature Glycosylation and Trafficking of Nicastrin Modulate Its Binding to Presenilins* 210 , 2002, The Journal of Biological Chemistry.

[14]  D. Selkoe,et al.  Proteolysis of Chimeric β-Amyloid Precursor Proteins Containing the Notch Transmembrane Domain Yields Amyloid β-like Peptides* , 2002, The Journal of Biological Chemistry.

[15]  G. Weinmaster,et al.  Ligand-induced signaling in the absence of furin processing of Notch1. , 2001, Developmental biology.

[16]  G. Rubin,et al.  Kuzbanian Controls Proteolytic Processing of Notch and Mediates Lateral Inhibition during Drosophila and Vertebrate Neurogenesis , 1997, Cell.

[17]  I. Greenwald,et al.  Additional evidence for an eight-transmembrane-domain topology for Caenorhabditis elegans and human presenilins. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[18]  Y. Yarden,et al.  Untangling the ErbB signalling network , 2001, Nature Reviews Molecular Cell Biology.

[19]  P. Fraser,et al.  The Presenilin 1 Protein Is a Component of a High Molecular Weight Intracellular Complex That Contains β-Catenin* , 1998, The Journal of Biological Chemistry.

[20]  Expression in mammalian cell cultures reveals interdependent, but distinct, functions for Star and Rhomboid proteins in the processing of the Drosophila transforming-growth-factor-alpha homologue Spitz. , 2002, The Biochemical journal.

[21]  L. Mei,et al.  Presenilin-dependent γ-Secretase-like Intramembrane Cleavage of ErbB4* , 2002, The Journal of Biological Chemistry.

[22]  J. Sklar,et al.  Calcium Depletion Dissociates and Activates Heterodimeric Notch Receptors , 2000, Molecular and Cellular Biology.

[23]  B. Hyman,et al.  Aspartate Mutations in Presenilin and γ‐Secretase Inhibitors Both Impair Notch1 Proteolysis and Nuclear Translocation with Relative Preservation of Notch1 Signaling , 2000, Journal of neurochemistry.

[24]  G. Struhl,et al.  Nicastrin is required for Presenilin-mediated transmembrane cleavage in Drosophila , 2001, Nature Cell Biology.

[25]  P. Rakic,et al.  The γ-secretase-generated intracellular domain of β-amyloid precursor protein binds Numb and inhibits Notch signaling , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[26]  J. Buxbaum,et al.  Tumor Necrosis Factor-α-converting Enzyme Is Required for Cleavage of erbB4/HER4* , 2000, The Journal of Biological Chemistry.

[27]  G. Serban,et al.  A presenilin‐1/γ‐secretase cleavage releases the E‐cadherin intracellular domain and regulates disassembly of adherens junctions , 2002, The EMBO journal.

[28]  Thomas C. Südhof,et al.  A Transcriptively Active Complex of APP with Fe65 and Histone Acetyltransferase Tip60 , 2001, Science.

[29]  D. Selkoe,et al.  Cell Surface Presenilin-1 Participates in the γ-Secretase-like Proteolysis of Notch* , 1999, The Journal of Biological Chemistry.

[30]  J. Priess,et al.  aph-2 encodes a novel extracellular protein required for GLP-1-mediated signaling. , 2000, Development.

[31]  Sangram S. Sisodia,et al.  γ-Secretase, notch, Aβ and alzheimer's disease: Where do the presenilins fit in? , 2002, Nature Reviews Neuroscience.

[32]  B. Yankner,et al.  Proteolytic release and nuclear translocation of Notch-1 are induced by presenilin-1 and impaired by pathogenic presenilin-1 mutations. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[33]  Min Xu,et al.  Photoactivated γ-secretase inhibitors directed to the active site covalently label presenilin 1 , 2000, Nature.

[34]  B. Ghetti,et al.  Presenilin-1 mutations of leucine 166 equally affect the generation of the Notch and APP intracellular domains independent of their effect on Aβ42 production , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[35]  A. Bernstein,et al.  Presenilins are required for γ-secretase cleavage of β-APP and transmembrane cleavage of Notch-1 , 2000, Nature Cell Biology.

[36]  J. Hardy,et al.  Glycine 384 is required for presenilin-1 function and is conserved in bacterial polytopic aspartyl proteases , 2000, Nature Cell Biology.

[37]  M. Nakao,et al.  CD44 cleavage induced by a membrane-associated metalloprotease plays a critical role in tumor cell migration , 1999, Oncogene.

[38]  D. Borchelt,et al.  Protein Topology of Presenilin 1 , 1996, Neuron.

[39]  G. Struhl,et al.  Requirements for presenilin-dependent cleavage of notch and other transmembrane proteins. , 2000, Molecular cell.

[40]  M. W. Young,et al.  Sequence of the notch locus of Drosophila melanogaster: relationship of the encoded protein to mammalian clotting and growth factors , 1986, Molecular and cellular biology.

[41]  Min Xu,et al.  Presenilin 1 is linked with gamma-secretase activity in the detergent solubilized state. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[42]  D. Selkoe,et al.  The cell biology of β-amyloid precursor protein and presenilin in Alzheimer's disease , 1998 .

[43]  D. Selkoe,et al.  Two transmembrane aspartates in presenilin-1 required for presenilin endoproteolysis and γ-secretase activity , 1999, Nature.

[44]  M. Fortini,et al.  Notch signaling. , 1995, Science.

[45]  I. Greenwald,et al.  LIN-12/Notch signaling: lessons from worms and flies. , 1998, Genes & development.

[46]  G. Weinmaster Notch signal transduction: a real rip and more. , 2000, Current opinion in genetics & development.

[47]  S. Tonegawa,et al.  Skeletal and CNS Defects in Presenilin-1-Deficient Mice , 1997, Cell.

[48]  A. Levey,et al.  Multiple Effects of Aspartate Mutant Presenilin 1 on the Processing and Trafficking of Amyloid Precursor Protein* , 2001, The Journal of Biological Chemistry.

[49]  P. Wong,et al.  Lack of requirement for Presenilin1 in Notch1 signaling , 1999, Current Biology.

[50]  D. Selkoe,et al.  The Intracellular Domain of the β-Amyloid Precursor Protein Is Stabilized by Fe65 and Translocates to the Nucleus in a Notch-like Manner* , 2001, The Journal of Biological Chemistry.

[51]  S. Eimer,et al.  A Loss of Function Mutant of the Presenilin Homologue SEL-12 Undergoes Aberrant Endoproteolysis in Caenorhabditis elegans and Increases Aβ42 Generation in Human Cells* , 2000, The Journal of Biological Chemistry.

[52]  D. Teplow,et al.  Separation of presenilin function in amyloid β-peptide generation and endoproteolysis of Notch , 2000, Neurobiology of Aging.

[53]  A. Parks,et al.  Ligand endocytosis drives receptor dissociation and activation in the Notch pathway. , 2000, Development.

[54]  P. Simpson,et al.  Requirement for dynamin during Notch signaling in Drosophila neurogenesis. , 1997, Developmental biology.

[55]  M. Metzstein,et al.  SUP-17, a Caenorhabditis elegans ADAM protein related to Drosophila KUZBANIAN, and its role in LIN-12/NOTCH signalling. , 1997, Development.

[56]  J. Herz,et al.  Proteolytic Processing of Low Density Lipoprotein Receptor-related Protein Mediates Regulated Release of Its Intracellular Domain* , 2002, The Journal of Biological Chemistry.

[57]  You-Qiang Song,et al.  Nicastrin binds to membrane-tethered Notch , 2001, Nature Cell Biology.

[58]  B. Shilo,et al.  A thousand and one roles for the Drosophila EGF receptor. , 1997, Trends in genetics : TIG.

[59]  M. Freeman,et al.  Regulated Intracellular Ligand Transport and Proteolysis Control EGF Signal Activation in Drosophila , 2001, Cell.

[60]  M. Freeman,et al.  Control of EGF receptor activation in Drosophila. , 1997, Trends in cell biology.

[61]  P. Kylsten,et al.  Providencia may help find a function for a novel, widespread protein family , 2000, Current Biology.

[62]  B. Shilo,et al.  Intracellular trafficking by Star regulates cleavage of the Drosophila EGF receptor ligand Spitz. , 2002, Genes & development.

[63]  H. Saya,et al.  Regulated CD44 Cleavage under the Control of Protein Kinase C, Calcium Influx, and the Rho Family of Small G Proteins* , 1999, The Journal of Biological Chemistry.

[64]  S. Artavanis-Tsakonas,et al.  Intracellular Cleavage of Notch Leads to a Heterodimeric Receptor on the Plasma Membrane , 1997, Cell.

[65]  D. Borchelt,et al.  Effects of PS1 Deficiency on Membrane Protein Trafficking in Neurons , 1998, Neuron.

[66]  D. Barnes,et al.  Nuclear expression of the c-erbB-4/HER-4 growth factor receptor in invasive breast cancers. , 2000, Cancer research.

[67]  P. S. St George-Hyslop,et al.  Mutation of conserved aspartates affect maturation of presenilin 1 and presenilin 2 complexes , 2000, Acta neurologica Scandinavica. Supplementum.

[68]  Huaxi Xu,et al.  Presenilin 1 Is Required for Maturation and Cell Surface Accumulation of Nicastrin* , 2002, The Journal of Biological Chemistry.

[69]  Raphael Kopan,et al.  Notch-1 signalling requires ligand-induced proteolytic release of intracellular domain , 1998, Nature.

[70]  H. Saya,et al.  Proteolytic release of CD44 intracellular domain and its role in the CD44 signaling pathway , 2001, The Journal of cell biology.

[71]  A. Israël,et al.  The Notch1 receptor is cleaved constitutively by a furin-like convertase. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[72]  A. Godwin,et al.  Proteolytic cleavage of the CD44 adhesion molecule in multiple human tumors. , 2002, The American journal of pathology.

[73]  Raphael Kopan,et al.  Embryonic lethality in mice homozygous for a processing-deficient allele of Notch1 , 2000, Nature.

[74]  A Cumano,et al.  A novel proteolytic cleavage involved in Notch signaling: the role of the disintegrin-metalloprotease TACE. , 2000, Molecular cell.

[75]  C. L. Harris,et al.  Evidence That Levels of Presenilins (PS1 and PS2) Are Coordinately Regulated by Competition for Limiting Cellular Factors* , 1997, The Journal of Biological Chemistry.

[76]  C. Masters,et al.  A novel epsilon-cleavage within the transmembrane domain of the Alzheimer amyloid precursor protein demonstrates homology with Notch processing. , 2002, Biochemistry.

[77]  A. Bernstein,et al.  Identification and Characterization of Presenilin-independent Notch Signaling* , 2002, The Journal of Biological Chemistry.

[78]  M. Fortini Notch and presenilin: a proteolytic mechanism emerges. , 2001, Current opinion in cell biology.

[79]  You-Qiang Song,et al.  Mutation of the conserved N‐terminal cysteine (Cys92) of human presenilin 1 causes increased Aβ42 secretion in mammalian cells but impaired Notch/lin‐I2 signalling in C. elegans , 2000, Neuroreport.

[80]  D. Levitan,et al.  APH-2/nicastrin functions in LIN-12/Notch signaling in the Caenorhabditis elegans somatic gonad. , 2001, Developmental biology.

[81]  Olivier Pourquié,et al.  New protease inhibitors prevent γ-secretase-mediated production of Aβ40/42 without affecting Notch cleavage , 2001, Nature Cell Biology.

[82]  C. Masters,et al.  The intramembrane cleavage site of the amyloid precursor protein depends on the length of its transmembrane domain , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[83]  B. Hyman,et al.  Effect of PS1 deficiency and an APP gamma-secretase inhibitor on Notch1 signaling in primary mammalian neurons. , 2001, Brain research. Molecular brain research.

[84]  S. Pimplikar,et al.  The γ-secretase-cleaved C-terminal fragment of amyloid precursor protein mediates signaling to the nucleus , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[85]  C. Ponting,et al.  Identification of a novel family of presenilin homologues. , 2002, Human molecular genetics.

[86]  Hugo Vanderstichele,et al.  Deficiency of presenilin-1 inhibits the normal cleavage of amyloid precursor protein , 1998, Nature.

[87]  M. Fortini,et al.  Nicastrin Is Required for γ-Secretase Cleavage of the Drosophila Notch Receptor , 2002 .

[88]  B. Strooper,et al.  Presenilins: molecular switches between proteolysis and signal transduction , 1999, Trends in Neurosciences.

[89]  P. Fraser,et al.  Mutation of conserved aspartates affects maturation of both aspartate mutant and endogenous presenilin 1 and presenilin 2 complexes. , 2000, The Journal of biological chemistry.

[90]  I. Greenwald,et al.  Membrane Topology of the C. elegans SEL-12 Presenilin , 1996, Neuron.

[91]  Robert A. Copeland,et al.  Presenilin-1 and -2 Are Molecular Targets for γ-Secretase Inhibitors* , 2000, The Journal of Biological Chemistry.

[92]  G. Boulianne,et al.  Drosophila presenilin Is Required for Neuronal Differentiation and Affects Notch Subcellular Localization and Signaling , 1999, The Journal of Neuroscience.

[93]  D. Selkoe,et al.  Transition-state analogue inhibitors of γ-secretase bind directly to presenilin-1 , 2000, Nature Cell Biology.

[94]  F. Checler,et al.  Endogenous β-amyloid production in presenilin-deficient embryonic mouse fibroblasts , 2001, Nature Cell Biology.

[95]  D. Price,et al.  Presenilin 1 is required for Notch 1 and Dll1 expression in the paraxial mesoderm , 1997, Nature.

[96]  D. Selkoe,et al.  Activity-dependent isolation of the presenilin– γ-secretase complex reveals nicastrin and a γ substrate , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[97]  D. Selkoe,et al.  Peptidomimetic probes and molecular modeling suggest that Alzheimer's gamma-secretase is an intramembrane-cleaving aspartyl protease. , 1999, Biochemistry.

[98]  L. Goldstein,et al.  Disruption of Axonal Transport and Neuronal Viability by Amyloid Precursor Protein Mutations in Drosophila , 2001, Neuron.

[99]  S. Artavanis-Tsakonas,et al.  Notch Signaling : Cell Fate Control and Signal Integration in Development , 1999 .

[100]  M. Fortini,et al.  Neurogenic phenotypes and altered Notch processing in Drosophila Presenilin mutants , 1999, Nature.

[101]  B. Strooper,et al.  Total inactivation of γ–secretase activity in presenilin-deficient embryonic stem cells , 2000, Nature Cell Biology.

[102]  Iva Greenwald,et al.  Presenilin is required for activity and nuclear access of Notch in Drosophila , 1999, Nature.

[103]  H. Mori,et al.  Membrane-Type 1 Matrix Metalloproteinase Cleaves Cd44 and Promotes Cell Migration , 2001, The Journal of cell biology.

[104]  Ruedi Aebersold,et al.  Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and βAPP processing , 2000, Nature.

[105]  Regulated intramembrane proteolysis takes another twist. , 2001, Developmental cell.

[106]  Kenji Matsuno,et al.  Notch signaling. , 1995, Science.

[107]  S. H. Kim,et al.  Characterization of a Presenilin-mediated Amyloid Precursor Protein Carboxyl-terminal Fragment γ , 2001, The Journal of Biological Chemistry.

[108]  C. Haass,et al.  Presenilin-1 differentially facilitates endoproteolysis of the β-amyloid precursor protein and Notch , 2000, Nature Cell Biology.

[109]  M. Tohyama,et al.  Absence of endoproteolysis but no effects on amyloid beta production by alternative splicing forms of presenilin-1, which lack exon 8 and replace D257A. , 2000, Brain research. Molecular brain research.

[110]  C. Blobel,et al.  Metalloprotease-disintegrins: modular proteins capable of promoting cell-cell interactions and triggering signals by protein-ectodomain shedding. , 1999, Journal of cell science.

[111]  D. St Johnston,et al.  Drosophila nicastrin is essential for the intramembranous cleavage of notch. , 2002, Developmental cell.

[112]  B. de Strooper,et al.  A physiologic signaling role for the γ-secretase-derived intracellular fragment of APP , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[113]  B. Martoglio,et al.  Identification of Signal Peptide Peptidase, a Presenilin-Type Aspartic Protease , 2002, Science.

[114]  U. Lendahl,et al.  Notch receptor cleavage depends on but is not directly executed by presenilins , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[115]  D. Selkoe,et al.  Amyloid-lowering isocoumarins are not direct inhibitors of γ-secretase , 2002, Nature Cell Biology.

[116]  K. Makino,et al.  Nuclear localization of EGF receptor and its potential new role as a transcription factor , 2001, Nature Cell Biology.

[117]  A. Goate,et al.  Posttranslational Modification and Plasma Membrane Localization of the Drosophila melanogaster Presenilin , 2000, Molecular and Cellular Neuroscience.

[118]  M. Wolfe,et al.  The Role of Presenilins in γ-Secretase Activity* , 2001, The Journal of Biological Chemistry.

[119]  H. Vanderstichele,et al.  The discrepancy between presenilin subcellular localization and γ-secretase processing of amyloid precursor protein , 2001, The Journal of cell biology.

[120]  G. Rubin,et al.  KUZ, a Conserved Metalloprotease-Disintegrin Protein with Two Roles in Drosophila Neurogenesis , 1996, Science.

[121]  M. Mattson A multi-talented secreted protein , 2001, Trends in Neurosciences.

[122]  Y. Ihara,et al.  Distinct Intramembrane Cleavage of the β-Amyloid Precursor Protein Family Resembling γ-Secretase-like Cleavage of Notch* , 2001, The Journal of Biological Chemistry.

[123]  Valerie A. Hale,et al.  APH-1 is a multipass membrane protein essential for the Notch signaling pathway in Caenorhabditis elegans embryos , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[124]  B. Strooper,et al.  Presenilins and the intramembrane proteolysis of proteins: facts and fiction , 2001, Nature Cell Biology.

[125]  Ronit Vogt Sionov,et al.  CD44: structure, function, and association with the malignant process. , 1997, Advances in cancer research.

[126]  L. Goldstein,et al.  Kinesin-mediated axonal transport of a membrane compartment containing β-secretase and presenilin-1 requires APP , 2001, Nature.

[127]  T. Golde,et al.  γ-Secretase, Evidence for Multiple Proteolytic Activities and Influence of Membrane Positioning of Substrate on Generation of Amyloid β Peptides of Varying Length* , 1999, The Journal of Biological Chemistry.

[128]  M. Fortini,et al.  Gene expression pattern Characterization of Drosophila Presenilin and its colocalization with Notch during development , 1998 .

[129]  B. de Strooper,et al.  The amyloid precursor protein (APP)‐cytoplasmic fragment generated by γ‐secretase is rapidly degraded but distributes partially in a nuclear fraction of neurones in culture , 2001, Journal of neurochemistry.

[130]  T. Golde,et al.  γ-Secretase Cleavage and Nuclear Localization of ErbB-4 Receptor Tyrosine Kinase , 2001, Science.

[131]  Duane D. Miller,et al.  Are presenilins intramembrane-cleaving proteases? Implications for the molecular mechanism of Alzheimer's disease. , 1999, Biochemistry.

[132]  Min Xu,et al.  Presenilin 1 is linked with γ-secretase activity in the detergent solubilized state , 2000, Neurobiology of Aging.

[133]  Christina A. Wilson,et al.  Presenilins are not required for Aβ42 production in the early secretory pathway , 2002, Nature Neuroscience.

[134]  Wei Xu,et al.  aph-1 and pen-2 Are Required for Notch Pathway Signaling, γ-Secretase Cleavage of βAPP, and Presenilin Protein Accumulation , 2002 .

[135]  S. L'Hernault,et al.  Mutation of a putative sperm membrane protein in Caenorhabditis elegans prevents sperm differentiation but not its associated meiotic divisions , 1992, The Journal of cell biology.

[136]  D. Borchelt,et al.  Endoproteolytic Processing and Stabilization of Wild-type and Mutant Presenilin* , 1997, The Journal of Biological Chemistry.

[137]  G. Carpenter,et al.  Constitutive Proteolysis of the ErbB-4 Receptor Tyrosine Kinase by a Unique, Sequential Mechanism , 1997, The Journal of cell biology.

[138]  T. Iwatsubo,et al.  Complex N‐glycosylated form of nicastrin is stabilized and selectively bound to presenilin fragments , 2002, FEBS letters.

[139]  S. Artavanis-Tsakonas,et al.  Complex cellular and subcellular regulation of notch expression during embryonic and imaginal development of Drosophila: implications for notch function , 1991, The Journal of cell biology.

[140]  William J. Ray,et al.  A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain , 1999, Nature.

[141]  Eugen C. Buehler,et al.  Sequence and analysis of chromosome 2 of the plant Arabidopsis thaliana , 1999, Nature.

[142]  I. Greenwald,et al.  Structure/function studies of lin-12/Notch proteins. , 1994, Current Opinion in Genetics and Development.

[143]  Klaus Fuchs,et al.  Presenilin‐dependent γ‐secretase processing of β‐amyloid precursor protein at a site corresponding to the S3 cleavage of Notch , 2001 .

[144]  C. Haass,et al.  Presenilin and nicastrin regulate each other and determine amyloid β-peptide production via complex formation , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[145]  Raphael Kopan,et al.  A ligand-induced extracellular cleavage regulates gamma-secretase-like proteolytic activation of Notch1. , 2000, Molecular cell.

[146]  M. W. Young,et al.  kuzbanian-mediated cleavage of Drosophila Notch. , 2002, Genes & development.

[147]  B. Strooper,et al.  Proteolytic processing and cell biological functions of the amyloid precursor protein. , 2000, Journal of cell science.