» Articles » PMID: 28736980

Diverse Roles for Glycosaminoglycans in Neural Patterning

Overview
Journal Dev Dyn
Publisher Wiley
Date 2017 Jul 25
PMID 28736980
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

The nervous system coordinates the functions of most multicellular organisms and their response to the surrounding environment. Its development involves concerted cellular interactions, including migration, axon guidance, and synapse formation. These processes depend on the molecular constituents and structure of the extracellular matrices (ECM). An essential component of ECMs are proteoglycans, i.e., proteins containing unbranched glycan chains known as glycosaminoglycans (GAGs). A defining characteristic of GAGs is their enormous molecular diversity, created by extensive modifications of the glycans during their biosynthesis. GAGs are widely expressed, and their loss can lead to catastrophic neuronal defects. Despite their importance, we are just beginning to understand the function and mechanisms of GAGs in neuronal development. In this review, we discuss recent evidence suggesting GAGs have specific roles in neuronal patterning and synaptogenesis. We examine the function played by the complex modifications present on GAG glycans and their roles in regulating different aspects of neuronal patterning. Moreover, the review considers the function of proteoglycan core proteins in these processes, stressing their likely role as co-receptors of different signaling pathways in a redundant and context-dependent manner. We conclude by discussing challenges and future directions toward a better understanding of these fascinating molecules during neuronal development. Developmental Dynamics 247:54-74, 2018. © 2017 Wiley Periodicals, Inc.

Citing Articles

Knockout of the intellectual disability-linked gene Hs6st2 in mice decreases heparan sulfate 6-O-sulfation, impairs dendritic spines of hippocampal neurons, and affects memory.

Moon S, Lee H, Archer-Hartmann S, Nagai N, Mubasher Z, Parappurath M Glycobiology. 2023; 34(2).

PMID: 38015989 PMC: 10969535. DOI: 10.1093/glycob/cwad095.


A novel cytoskeletal action of xylosides.

Mencio C, Tilve S, Suzuki M, Higashi K, Katagiri Y, Geller H PLoS One. 2022; 17(6):e0269972.

PMID: 35763520 PMC: 9239447. DOI: 10.1371/journal.pone.0269972.


Specific N-glycans regulate an extracellular adhesion complex during somatosensory dendrite patterning.

Rahman M, Ramirez-Suarez N, Diaz-Balzac C, Bulow H EMBO Rep. 2022; 23(7):e54163.

PMID: 35586945 PMC: 9253746. DOI: 10.15252/embr.202154163.


Imaging Glycosaminoglycan Modification Patterns In Vivo.

Bulow H Methods Mol Biol. 2021; 2303:539-557.

PMID: 34626406 DOI: 10.1007/978-1-0716-1398-6_42.


The HSPG syndecan is a core organizer of cholinergic synapses.

Zhou X, Vachon C, Cizeron M, Romatif O, Bulow H, Jospin M J Cell Biol. 2021; 220(9).

PMID: 34213535 PMC: 8258370. DOI: 10.1083/jcb.202011144.


References
1.
Martini F, Valiente M, Lopez Bendito G, Szabo G, Moya F, Valdeolmillos M . Biased selection of leading process branches mediates chemotaxis during tangential neuronal migration. Development. 2008; 136(1):41-50. DOI: 10.1242/dev.025502. View

2.
Sundararajan L, Norris M, Lundquist E . SDN-1/Syndecan Acts in Parallel to the Transmembrane Molecule MIG-13 to Promote Anterior Neuroblast Migration. G3 (Bethesda). 2015; 5(8):1567-74. PMC: 4528313. DOI: 10.1534/g3.115.018770. View

3.
Hao J, Yu T, Fujisawa K, Culotti J, Mitani S, Moulder G . C. elegans slit acts in midline, dorsal-ventral, and anterior-posterior guidance via the SAX-3/Robo receptor. Neuron. 2001; 32(1):25-38. DOI: 10.1016/s0896-6273(01)00448-2. View

4.
Coles C, Shen Y, Tenney A, Siebold C, Sutton G, Lu W . Proteoglycan-specific molecular switch for RPTPσ clustering and neuronal extension. Science. 2011; 332(6028):484-8. PMC: 3154093. DOI: 10.1126/science.1200840. View

5.
Aono S, Tokita Y, Shuo T, Yamauchi S, Matsui F, Nakanishi K . Glycosylation site for chondroitin sulfate on the neural part-time proteoglycan, neuroglycan C. J Biol Chem. 2004; 279(45):46536-41. DOI: 10.1074/jbc.M403263200. View