This project will focus on chondroitin sulfate glycosaminoglycans (CS GAGs), a class of polysaccharides that play important roles in development, viral invasion, cancer, and spinal cord injury. CS GAGs display diverse sulfation patterns that are spatiotemporally regulated in vivo. However, efforts to identify functions for specific sulfation motifs have been hampered by the structural complexity of CS and a lack of tools. In this grant, we will combine the power of both organic chemistry and biology to overcome these challenges and identify novel functions for specific motifs in the nervous system. The broad objectives of this program are to: (1) advance a fundamental understanding of the structure-function relationships of CS GAGs, (2) understand the roles of CS GAGs in neuroplasticity and regeneration, and (3) develop new approaches to study and manipulate GAG-mediated biological processes, with the long-term goal of stimulating synaptic plasticity and neuronal repair. In the last granting period, we developed a set of chemical tools to study specific sulfation motifs and discovered that a particular motif, CS-E, inhibits axon regeneration after spinal cord injury. Blocking the CS-E motif using an anti-CS-E antibody stimulated axon regeneration in vivo. Moreover, we found that this same motif repels axons and plays a critical role in neural circuit formation during brain development. An important observation from this work was that the activity of CS-E required its interaction with cell-surface receptors and activation of specific inhibitory signaling pathways in neurons. In the present grant, we will develop new approaches to modulate the interactions of CS-E with neuronal receptors, including the viral-mediated delivery of single-chain anti-CS-E antibodies, small- molecule sulfotransferase inhibitors, and glycopolymer mimetics (Aim 1). We will study how CS-E regulates protein signaling complexes, with a particular focus on semaphorin-3A/neuropilin-1/plexin A (Sema3A/Nrp1/PlxnA) and ephrin/Eph receptor (Efn/Eph) complexes (Aims 2a and 3a). Finally, we will investigate the ability of the agents developed in Aim 1 to promote neuroplasticity in the visual cortex (Aims 2b,c) and axon regeneration after spinal cord injury (Aim 3b). These studies are expected to provide new chemical tools to advance an understanding of GAGs and fundamentally change how CS GAGs are viewed - from being static, passive molecules to ligands that actively regulate important signaling pathways. Finally, if successful, the agents developed in Aim 1 could lead to novel therapeutic strategies for stimulating neuronal plasticity and repair in the case of aging, injury, and disease.

Public Health Relevance

This research seeks to understand how the structure of chondroitin sulfate glycosaminoglycans regulates fundamental biological processes, such as protein recognition and regulation, signal transduction, brain development, and regeneration after injury. Through the discovery of novel small molecules, proteins and pathways involved in these processes, this work may aid ultimately in the development of new therapeutic approaches to stimulate neuronal repair in response to aging, injury, and disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM093627-08
Application #
9488501
Study Section
Synthetic and Biological Chemistry A Study Section (SBCA)
Program Officer
Marino, Pamela
Project Start
2010-04-01
Project End
2019-05-31
Budget Start
2018-06-01
Budget End
2019-05-31
Support Year
8
Fiscal Year
2018
Total Cost
Indirect Cost
Name
California Institute of Technology
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
009584210
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Griffin, Matthew E; Hsieh-Wilson, Linda C (2016) Glycan Engineering for Cell and Developmental Biology. Cell Chem Biol 23:108-121
Miller, Gregory M; Hsieh-Wilson, Linda C (2015) Sugar-dependent modulation of neuronal development, regeneration, and plasticity by chondroitin sulfate proteoglycans. Exp Neurol 274:115-25
Pulsipher, Abigail; Griffin, Matthew E; Stone, Shannon E et al. (2015) Long-lived engineering of glycans to direct stem cell fate. Angew Chem Int Ed Engl 54:1466-70
Pulsipher, Abigail; Griffin, Matthew E; Stone, Shannon E et al. (2014) Directing neuronal signaling through cell-surface glycan engineering. J Am Chem Soc 136:6794-7
Matho, Michael H; de Val, Natalia; Miller, Gregory M et al. (2014) Murine anti-vaccinia virus D8 antibodies target different epitopes and differ in their ability to block D8 binding to CS-E. PLoS Pathog 10:e1004495
Griffin, Matthew E; Hsieh-Wilson, Linda C (2013) Synthetic probes of glycosaminoglycan function. Curr Opin Chem Biol 17:1014-22
Oh, Young In; Sheng, Gloria J; Chang, Shuh-Kuen et al. (2013) Tailored glycopolymers as anticoagulant heparin mimetics. Angew Chem Int Ed Engl 52:11796-9
Sheng, Gloria J; Oh, Young In; Chang, Shuh-Kuen et al. (2013) Tunable heparan sulfate mimetics for modulating chemokine activity. J Am Chem Soc 135:10898-901
Dick, Gunnar; Tan, Chin Lik; Alves, Joao Nuno et al. (2013) Semaphorin 3A binds to the perineuronal nets via chondroitin sulfate type E motifs in rodent brains. J Biol Chem 288:27384-95
Rogers, Claude J; Hsieh-Wilson, Linda C (2012) Microarray method for the rapid detection of glycosaminoglycan-protein interactions. Methods Mol Biol 808:321-36

Showing the most recent 10 out of 15 publications