Heparan sulfate proteoglycans: The sweet side of development turns sour in mucopolysaccharidoses

被引:68
作者
De Pasquale, Valeria [1 ]
Pavone, Luigi Michele [1 ]
机构
[1] Univ Naples Federico II, Med Sch, Dept Mol Med & Med Biotechnol, Via S Pansini 5, I-80131 Naples, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2019年 / 1865卷 / 11期
关键词
Heparan sulfate proteoglycans (HSPGs); Glycosaminoglycans (GAGS); Central nervous system (CNS) and skeletal system development; Lysosomal storage diseases (LSDs); Mucopolysaccharidoses (MPSs); FIBROBLAST-GROWTH; LYSOSOMAL STORAGE; AXON GUIDANCE; CELL-SURFACE; MOUSE MODEL; MITOCHONDRIAL DEFECTS; SKELETAL-MUSCLE; JOINT DISEASE; BONE; STEM;
D O I
10.1016/j.bbadis.2019.165539
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Heparan sulfate proteoglycans (HSPGs) are complex carbohydrate-modified proteins ubiquitously expressed on cell surfaces, extracellular matrix and basement membrane of mammalian tissues. Beside to serve as structural constituents, they regulate multiple cellular activities. A critical involvement of HSPGs in development has been established, and perturbations of HSPG-dependent pathways are associated with many human diseases. Recent evidence suggest a role of HSPGs in the pathogenesis of mucopolysaccharidoses (MPSs) where the accumulation of undigested HS results in the loss of cellular functions, tissue damage and organ dysfunctions accounting for clinical manifestations which include central nervous system (CNS) involvement, degenerative joint disease and reduced bone growth. Current therapies are not curative but only ameliorate the disease symptoms. Here, we highlight the link between HSPG functions in the development of CNS and musculoskeletal structures and the etiology of some MPS phenotypes, suggesting that HSPGs may represent potential targets for the therapy of such incurable diseases.
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页数:11
相关论文
共 157 条
[1]   Syndecans - key regulators of cell signaling and biological functions [J].
Afratis, Nikolaos A. ;
Nikitovic, Dragana ;
Multhaupt, Hinke A. B. ;
Theocharis, Achilleas D. ;
Couchman, John R. ;
Karamanos, Nikos K. .
FEBS JOURNAL, 2017, 284 (01) :27-41
[2]   Astrocyte glypicans 4 and 6 promote formation of excitatory synapses via GluA1 AMPA receptors [J].
Allen, Nicola J. ;
Bennett, Mariko L. ;
Foo, Lynette C. ;
Wang, Gordon X. ;
Chakraborty, Chandrani ;
Smith, Stephen J. ;
Barres, Ben A. .
NATURE, 2012, 486 (7403) :410-+
[3]   Augmented synthesis and differential localization of heparan sulfate proteoglycans in Duchenne muscular dystrophy [J].
Alvarez, K ;
Fadic, R ;
Brandan, E .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2002, 85 (04) :703-713
[4]   Mucopolysaccharide diseases: A complex interplay between neuroinflammation, microglial activation and adaptive immunity [J].
Archer, Louise D. ;
Langford-Smith, Kia J. ;
Bigger, Brian W. ;
Fildes, James E. .
JOURNAL OF INHERITED METABOLIC DISEASE, 2014, 37 (01) :1-12
[5]   Lysosomal disorders: From storage to cellular damage [J].
Ballabio, Andrea ;
Gieselmann, Volkmar .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2009, 1793 (04) :684-696
[6]   Sweet on Hedgehogs: Regulatory Roles of Heparan Sulfate Proteoglycans in Hedgehog-Dependent Cell Proliferation and Differentiation [J].
Bandari, Shyam ;
Exner, Sebastian ;
Ortmann, Corinna ;
Bachvarova, Velina ;
Vortkamp, Andrea ;
Grobe, Kay .
CURRENT PROTEIN & PEPTIDE SCIENCE, 2015, 16 (01) :66-76
[7]   Extracellular matrix components: An intricate network of possible biomarkers for lysosomal storage disorders? [J].
Batzios, Spyros P. ;
Zafeiriou, Dimitrios I. ;
Papakonstantinou, Eleni .
FEBS LETTERS, 2013, 587 (08) :1258-1267
[8]  
Bellesso S, 2018, HUM MOL GENET, V27, P2262, DOI 10.1093/hmg/ddy131
[9]   Pathophysiology of neuropathic lysosomal storage disorders [J].
Bellettato, Cinzia Maria ;
Scarpa, Maurizio .
JOURNAL OF INHERITED METABOLIC DISEASE, 2010, 33 (04) :347-362
[10]   Bone development [J].
Berendsen, Agnes D. ;
Olsen, Bjorn R. .
BONE, 2015, 80 :14-18