Chondroitin Sulfate Proteoglycans: Structure-Function Relationship with Implication in Neural Development and Brain Disorders

被引:75
作者
Avram, Speranta [1 ]
Shaposhnikov, Sergey [2 ]
Buiu, Catalin [1 ,3 ]
Mernea, Maria [1 ]
机构
[1] Univ Bucharest, Fac Biol, Anat Anim Physiol & Biophys Dept, Bucharest 050095, Romania
[2] Norgenotech AS, N-2848 Skreia, Norway
[3] Univ Politehn Bucuresti, Fac Automat Control & Comp, Automat Control & Syst Engn Dept, Bucharest 060042, Romania
关键词
C-TYPE LECTINS; EXTRACELLULAR-MATRIX MOLECULES; HYALURONAN-BINDING DOMAINS; CELL-ADHESION; ANTIPSYCHOTIC-DRUGS; BIPOLAR DISORDER; INHIBITORY-ACTIVITY; COMMON VARIATION; DENDRITIC CELLS; NEURITE GROWTH;
D O I
10.1155/2014/642798
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chondroitin sulfate proteoglycans (CSPGs) are extracellular matrix components that contain two structural parts with distinct functions: a protein core and glycosaminoglycan (GAG) side chains. CSPGs are known to be involved in important cell processes like cell adhesion and growth, receptor binding, or cell migration. It is recognized that the presence of CSPGs is critical in neuronal growth mechanisms including axon guidance following injury of nervous system components such as spinal cord and brain. CSPGs are upregulated in the central nervous system after injury and participate in the inhibition of axon regeneration mainly through their GAG side chains. Recently, it was shown that some CSPGs members like aggrecan, versican, and neurocan were strongly involved in brain disorders like bipolar disorder (BD), schizophrenia, and ADHD. In this paper, we present the chemical structure-biological functions relationship of CSPGs, both in health state and in genetic disorders, addressing methods represented by genome-wide and crystallographic data as well as molecular modeling and quantitative structure-activity relationship.
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页数:11
相关论文
共 94 条
[1]  
[Anonymous], PYMOL MOL GRAPH SYST
[2]   The Different Roles of Aggrecan Interaction Domains [J].
Aspberg, Anders .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2012, 60 (12) :987-996
[3]   Quantitative structure - activity relationship studies on membrane receptors inhibition by antipsychotic drugs. Application to schizophrenia treatment [J].
Avram, Speranta ;
Berner, Heinz ;
Milac, Adina L. ;
Wolschann, Peter .
MONATSHEFTE FUR CHEMIE, 2008, 139 (04) :407-426
[4]   3D-QSAR study indicates an enhancing effect of membrane ions on psychiatric drugs targeting serotonin receptor 5-HT1A [J].
Avram, Speranta ;
Milac, Adina-Luminita ;
Mihailescu, Dan .
MOLECULAR BIOSYSTEMS, 2012, 8 (05) :1418-1425
[5]   QSAR-CoMSIA applied to antipsychotic drugs with their dopamine D2 and serotonine 5HT2A membrane receptors [J].
Avram, Speranta ;
Duda-Seiman, Daniel ;
Borcan, Florin ;
Wolschann, Peter .
JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 2011, 76 (02) :263-281
[6]   Evaluation of Antimicrobial Activity of New Mastoparan Derivatives Using QSAR and Computational Mutagenesis [J].
Avram, Speranta ;
Duda-Seiman, Daniel ;
Borcan, Florin ;
Radu, Beatrice ;
Duda-Seiman, Corina ;
Mihailescu, Dan .
INTERNATIONAL JOURNAL OF PEPTIDE RESEARCH AND THERAPEUTICS, 2011, 17 (01) :7-17
[7]   Proteoglycans in the developing brain: New conceptual insights for old proteins [J].
Bandtlow, CE ;
Zimmermann, DR .
PHYSIOLOGICAL REVIEWS, 2000, 80 (04) :1267-1290
[8]   Neurocan contributes to the molecular heterogeneity of the perinodal ECM [J].
Bekku, Yoko ;
Oohashi, Toshitaka .
ARCHIVES OF HISTOLOGY AND CYTOLOGY, 2010, 73 (02) :95-102
[9]   Molecular surface generation using a variable-radius solvent probe [J].
Bhat, S ;
Purisima, EO .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2006, 62 (01) :244-261
[10]   Axonal Regrowth after Spinal Cord Injury via Chondroitinase and the Tissue Plasminogen Activator (tPA)/Plasmin System [J].
Bukhari, Noreen ;
Torres, Luisa ;
Robinson, John K. ;
Tsirka, Stella E. .
JOURNAL OF NEUROSCIENCE, 2011, 31 (42) :14931-14943