Multifunctionality of extracellular and cell surface heparan sulfate proteoglycans

scientific article published on 24 July 2009

Multifunctionality of extracellular and cell surface heparan sulfate proteoglycans is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P356DOI10.1007/S00018-009-0096-1
P698PubMed publication ID19629389
P5875ResearchGate publication ID26692602

P2093author name stringMary C Farach-Carson
Daniel D Carson
Catherine Kirn-Safran
P2860cites workHeparan sulfate structure in mice with genetically modified heparan sulfate productionQ80413581
Microfibrils at basement membrane zones interact with perlecan via fibrillin-1Q81289350
Transgenic or tumor-induced expression of heparanase upregulates sulfation of heparan sulfateQ81474966
Heparan sulfate of perlecan is involved in glomerular filtrationQ81716389
Reduced perlecan expression and accumulation in human carotid atherosclerotic lesionsQ83168047
PI-88: a novel inhibitor of angiogenesisQ94801394
Secreted sulfatases Sulf1 and Sulf2 have overlapping yet essential roles in mouse neonatal survivalQ21144445
GlypicansQ21183908
The putative tumor suppressors EXT1 and EXT2 form a stable complex that accumulates in the Golgi apparatus and catalyzes the synthesis of heparan sulfateQ22011093
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)Q24273425
Characterization of Slit protein interactions with glypican-1Q24291266
Heparanase mediates cell adhesion independent of its enzymatic activityQ24303492
Structural recognition by recombinant human heparanase that plays critical roles in tumor metastasis. Hierarchical sulfate groups with different effects and the essential target disulfated trisaccharide sequenceQ24306149
Cloning and characterization of two extracellular heparin-degrading endosulfatases in mice and humansQ24309373
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndromeQ24320198
Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidneyQ24540314
Sulfatase 2 up-regulates glypican 3, promotes fibroblast growth factor signaling, and decreases survival in hepatocellular carcinomaQ24651026
Heparan sulphate synthetic and editing enzymes in ovarian cancerQ24653774
Gene trap disruption of the mouse heparan sulfate 6-O-endosulfatase gene, Sulf2Q24673634
Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativityQ24673740
QSulf1 remodels the 6-O sulfation states of cell surface heparan sulfate proteoglycans to promote Wnt signalingQ24675509
Perlecan maintains the integrity of cartilage and some basement membranesQ24680954
Delayed wound repair and impaired angiogenesis in mice lacking syndecan-4Q24681644
Heparan sulfate biosynthesis enzymes EXT1 and EXT2 affect NDST1 expression and heparan sulfate sulfationQ28115828
Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndromeQ28139404
Perlecan is essential for cartilage and cephalic developmentQ28146148
The splice variants of vascular endothelial growth factor (VEGF) and their receptorsQ28200155
Cloning of an immunoglobulin family adhesion molecule selectively expressed by endothelial cellsQ28208656
Signalling by HGF/SF and Met: the role of heparan sulphate co-receptorsQ28240994
Glypican-1 as an Abeta binding HSPG in the human brain: its localization in DIG domains and possible roles in the pathogenesis of Alzheimer's diseaseQ28256486
Integral membrane heparan sulfate proteoglycansQ28262453
The Frizzled CRD domain is conserved in diverse proteins including several receptor tyrosine kinasesQ28274567
Processing by convertases is not required for glypican-3-induced stimulation of hepatocellular carcinoma growthQ28277212
Defective neuromuscular synaptogenesis in agrin-deficient mutant miceQ28280786
BMP-1/Tolloid-like metalloproteases process endorepellin, the angiostatic C-terminal fragment of perlecanQ28297745
Agrin is a chimeric proteoglycan with the attachment sites for heparan sulfate/chondroitin sulfate located in two multiple serine-glycine clustersQ28505873
Structurally altered basement membranes and hydrocephalus in a type XVIII collagen deficient mouse lineQ28507183
Lack of collagen XVIII/endostatin results in eye abnormalitiesQ28511317
WARP is a novel multimeric component of the chondrocyte pericellular matrix that interacts with perlecanQ28512220
Alternatively spliced isoforms of nerve- and muscle-derived agrin: their roles at the neuromuscular junctionQ28513062
The molecular phenotype of heparan sulfate in the Hs2st-/- mutant mouseQ28513833
Characterization of heparanase from a rat parathyroid cell lineQ28566513
Disruption of gastrulation and heparan sulfate biosynthesis in EXT1-deficient miceQ28586958
Abnormal mast cells in mice deficient in a heparin-synthesizing enzymeQ28586968
Altered hematopoiesis in glypican-3-deficient mice results in decreased osteoclast differentiation and a delay in endochondral ossificationQ28587283
Mammalian Brain Morphogenesis and Midline Axon Guidance Require Heparan SulfateQ28588474
Renal agenesis in mice homozygous for a gene trap mutation in the gene encoding heparan sulfate 2-sulfotransferaseQ28589603
Targeted disruption of a murine glucuronyl C5-epimerase gene results in heparan sulfate lacking L-iduronic acid and in neonatal lethalityQ28591170
Defective heparan sulfate biosynthesis and neonatal lethality in mice lacking N-deacetylase/N-sulfotransferase-1Q28591609
Mice deficient in Ext2 lack heparan sulfate and develop exostosesQ28592253
Mice deficient in heparan sulfate 6-O-sulfotransferase-1 exhibit defective heparan sulfate biosynthesis, abnormal placentation, and late embryonic lethalityQ28592475
Cerebral hypoplasia and craniofacial defects in mice lacking heparan sulfate Ndst1 gene functionQ28592534
Mice deficient in heparan sulfate 3-O-sulfotransferase-1: Normal hemostasis with unexpected perinatal phenotypesQ29041315
Order out of chaos: assembly of ligand binding sites in heparan sulfateQ29620085
Agrin and neuregulin, expanding roles and implications for therapeuticsQ37068224
Novel interactions of perlecan: unraveling perlecan's role in angiogenesis.Q37094730
Fibrinogen facilitates the anti-tumor effect of nonnative endostatinQ37177297
Revisiting the glomerular charge barrier in the molecular era.Q37228168
Heparanase: one molecule with multiple functions in cancer progressionQ37228578
Muscular dystrophies due to glycosylation defectsQ37329563
Heparan sulfate in perlecan promotes mouse atherosclerosis: roles in lipid permeability, lipid retention, and smooth muscle cell proliferationQ37395446
QSulf1, a heparan sulfate 6-O-endosulfatase, inhibits fibroblast growth factor signaling in mesoderm induction and angiogenesisQ37415156
Essential and separable roles for Syndecan-3 and Syndecan-4 in skeletal muscle development and regeneration.Q37522362
Mice lacking the syndecan-3 gene are resistant to diet-induced obesity.Q37591908
Characterization of heparan sulfate oligosaccharides that bind to hepatocyte growth factorQ38288128
6-O-sulfation of heparan sulfate differentially regulates various fibroblast growth factor-dependent signalings in cultureQ38293479
Loss of HSulf-1 expression enhances autocrine signaling mediated by amphiregulin in breast cancer.Q38303667
Heparan sulfate Ndst1 gene function variably regulates multiple signaling pathways during mouse developmentQ38306324
Sequence analysis of heparan sulphate and heparin oligosaccharidesQ38325522
Structure of a heparan sulphate oligosaccharide that binds to basic fibroblast growth factorQ38327052
Perlecan binds to the beta-amyloid proteins (A beta) of Alzheimer's disease, accelerates A beta fibril formation, and maintains A beta fibril stability.Q39115406
Overproduction of perlecan core protein in cultured cells and transgenic miceQ39121464
Collagen XVIII/endostatin is essential for vision and retinal pigment epithelial function.Q39315528
Tyrosine dephosphorylation of the syndecan-1 PDZ binding domain regulates syntenin-1 recruitmentQ39882042
The frizzled extracellular domain is a ligand for Van Gogh/Stbm during nonautonomous planar cell polarity signalingQ39937859
A novel peptide sequence in perlecan domain IV supports cell adhesion, spreading and FAK activationQ40053261
Heparanase expression and function during early pregnancy in mice.Q40131935
Endorepellin in vivo: targeting the tumor vasculature and retarding cancer growth and metabolismQ40208428
Syndecan-2 is expressed in the microvasculature of gliomas and regulates angiogenic processes in microvascular endothelial cellsQ40297851
Structure and laminin-binding specificity of the NtA domain expressed in eukaryotic cells.Q40461722
Sodium channel beta1 subunits promote neurite outgrowth in cerebellar granule neuronsQ40510241
Differential regulation of hepatocyte growth factor/scatter factor by cell surface proteoglycans and free glycosaminoglycan chainsQ40952245
Acetylcholine receptors and the cytoskeletal connectionQ41143605
The core protein of growth plate perlecan binds FGF-18 and alters its mitogenic effect on chondrocytesQ41489080
Processing by proprotein convertases is required for glypican-3 modulation of cell survival, Wnt signaling, and gastrulation movementsQ41871371
Molecular behavior adapts to context: heparanase functions as an extracellular matrix-degrading enzyme or as a T cell adhesion molecule, depending on the local pH.Q41880677
Syndecan-3-deficient mice exhibit enhanced LTP and impaired hippocampus-dependent memoryQ42526526
Motifs of cadherin- and fibronectin type III-related sequences and evolution of the receptor-type-protein tyrosine kinases: sequence similarity between proto-oncogene ret and cadherin familyQ42616776
Reduced perlecan in mice results in chondrodysplasia resembling Schwartz-Jampel syndromeQ42832135
HIP/RPL29 antagonizes VEGF and FGF2 stimulated angiogenesis by interfering with HS-dependent responses.Q43096150
Defects in keratinocyte activation during wound healing in the syndecan-1-deficient mouseQ44204092
Lack of type XVIII collagen results in anterior ocular defectsQ44606546
Transgenic expression of mammalian heparanase uncovers physiological functions of heparan sulfate in tissue morphogenesis, vascularization, and feeding behaviorQ44760488
Heparan sulfate synthesized by mouse embryonic stem cells deficient in NDST1 and NDST2 is 6-O-sulfated but contains no N-sulfate groupsQ45023582
Inhibition by the soluble syndecan-1 ectodomains delays wound repair in mice overexpressing syndecan-1.Q47283049
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).Q47810194
Heparan sulphation patterns generated by specific heparan sulfotransferase enzymes direct distinct aspects of retinal axon guidance at the optic chiasm.Q48484123
Amyloid beta induces cellular relocalization and production of agrin and glypican-1.Q48790464
Perlecan is critical for heart stability.Q48975311
Heparanase is expressed in osteoblastic cells and stimulates bone formation and bone mass.Q51816706
Juvenile syndecan-1 null mice are protected from carcinogen-induced tumor development.Q52007642
Heparan sulfate biosynthetic gene Ndst1 is required for FGF signaling in early lens development.Q52575004
Agrin binds alpha-synuclein and modulates alpha-synuclein fibrillation.Q53271067
Interaction between beta-amyloid protein and heparan sulfate proteoglycans from the cerebral capillary basement membrane in Alzheimer's disease.Q53397484
Agrin is highly expressed by chondrocytes and is required for normal growth.Q53581329
Evidence of neuronal migration disorders in Knobloch syndrome: Clinical and molecular analysis of two novel familiesQ53654237
[Adhesive glycoproteins of the extracellular matrix]Q55476925
Spectrum ofHSPG2(Perlecan) mutations in patients with Schwartz-Jampel syndromeQ57639997
Syndecan-4 deficiency impairs the fetal vessels in the placental labyrinthQ58211928
Exploitation of syndecan-1 shedding by Pseudomonas aeruginosa enhances virulenceQ59092900
Evidence of a dosage effect and a physiological endplate acetylcholinesterase deficiency in the first mouse models mimicking Schwartz–Jampel syndrome neuromyotoniaQ62023500
Purification and characterization of placental heparanase and its expression by cultured cytotrophoblastsQ73549528
Syndecan-1 is required for Wnt-1-induced mammary tumorigenesis in miceQ73977149
Heparanase as mediator of angiogenesis: mode of actionQ74101720
Increased intimal hyperplasia and smooth muscle cell proliferation in transgenic mice with heparan sulfate-deficient perlecanQ75318637
Transgenic expression of the EXT2 gene in developing chondrocytes enhances the synthesis of heparan sulfate and bone formation in miceQ77912584
Double knockout mice reveal a lack of major functional compensation between collagens XV and XVIIIQ79291370
Identification of proteoglycan-binding proteinsQ79369814
Syndecan-1/CD147 association is essential for cyclophilin B-induced activation of p44/42 mitogen-activated protein kinases and promotion of cell adhesion and chemotaxisQ79700174
A polymorphism in the angiogenesis inhibitor, endostatin, in lung cancer susceptibilityQ80135645
Altered heparan sulfate structure in mice with deleted NDST3 gene function.Q30488977
Heparan sulfate: lessons from knockout miceQ30689506
Cloning, expression, and purification of mouse heparanaseQ33185312
Characterization of growth factor-binding structures in heparin/heparan sulfate using an octasaccharide libraryQ33196496
Eosinophil major basic protein: first identified natural heparanase-inhibiting proteinQ33202066
Structural specificity in a FGF7-affinity purified heparin octasaccharide required for formation of a complex with FGF7 and FGFR2IIIbQ33228058
Preparation and use of microarrays containing synthetic heparin oligosaccharides for the rapid analysis of heparin-protein interactions.Q33261613
The elusive functions of proteoglycans: in vivo veritasQ33825069
Extracellular matrix components in retrocorneal fibrous membrane in comparison to corneal endothelium and Descemet's membrane.Q33895529
A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinomaQ34095548
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumoursQ34108448
Pathogenesis of beta2-microglobulin amyloidosisQ34124669
Processing of macromolecular heparin by heparanaseQ34210691
Molecular properties and involvement of heparanase in cancer metastasis and angiogenesisQ34328744
Interaction of hepatocyte growth factor with heparan sulfate. Elucidation of the major heparan sulfate structural determinantsQ34339506
Cloning of cDNA and genomic DNA encoding human type XVIII collagen and localization of the alpha 1(XVIII) collagen gene to mouse chromosome 10 and human chromosome 21.Q34341595
Proteoglycans: pericellular and cell surface multireceptors that integrate external stimuli in the mammary glandQ34362776
Physiological role of collagen XVIII and endostatinQ34414325
Merging extracellular domains: fold prediction for laminin G-like and amino-terminal thrombospondin-like modules based on homology to pentraxinsQ34457974
Sulf1 expression pattern and its role in cartilage and joint developmentQ34576249
Heparan sulfate and development: differential roles of the N-acetylglucosamine N-deacetylase/N-sulfotransferase isozymesQ34989516
New insights into the roles of agrinQ35097331
Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivityQ35928165
Matrix revolutions: "tails" of basement-membrane components with angiostatic functionsQ36010882
Heparan sulfate proteoglycans: key players in cartilage biology.Q36098139
Linker molecules between laminins and dystroglycan ameliorate laminin-alpha2-deficient muscular dystrophy at all disease stagesQ36118063
Endostatin signaling and regulation of endothelial cell-matrix interactionsQ36226744
Assembly of the postsynaptic membrane at the neuromuscular junction: paradigm lostQ36357189
Syndecans in wound healing, inflammation and vascular biologyQ36649995
The heparanome--the enigma of encoding and decoding heparan sulfate sulfation.Q36751291
Perlecan--a multifunctional extracellular proteoglycan scaffold.Q36795158
PI-88 and novel heparan sulfate mimetics inhibit angiogenesis.Q36880841
Constitutive and accelerated shedding of murine syndecan-1 is mediated by cleavage of its core protein at a specific juxtamembrane siteQ36898627
Diverse cell signaling events modulated by perlecan.Q37020797
P433issue21
P921main subjectheparan sulfate proteoglycansQ66589633
P304page(s)3421-3434
P577publication date2009-07-24
P1433published inCellular and Molecular Life SciencesQ5058352
P1476titleMultifunctionality of extracellular and cell surface heparan sulfate proteoglycans
P478volume66

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