Target intelligence / Profile preview

Chondroitin sulfate proteoglycan (CSPG) (CSPG)

Target
CSPG
Molecular classification
Extracellular matrix protein, Proteoglycan
01

Overview

Chondroitin sulfate proteoglycans (CSPGs) are a major class of extracellular matrix (ECM) molecules that become highly upregulated following central nervous system (CNS) injury, forming a dense inhibitory environment known as the glial scar (Silver & Miller, 2004). These molecules consist of a core protein with covalently attached glycosaminoglycan (GAG) side chains, which are primarily responsible for their potent inhibition of axonal regeneration and plasticity (Dyck & Karimi-Abdolrezaee, 2015). In the healthy brain, CSPGs contribute to structural integrity and the formation of perineuronal nets, but after trauma, they act as physical and chemical barriers to repair. Therapeutic strategies targeting CSPGs include enzymatic digestion of the inhibitory GAG chains using Chondroitinase ABC or blocking the interaction between CSPGs and their neuronal receptors, such as Protein Tyrosine Phosphatase sigma (PTPσ) (Lang et al., 2015). By neutralizing the inhibitory properties of the glial scar, these interventions aim to promote functional recovery in conditions like spinal cord injury and stroke. Current research is focused on improving the delivery of these agents and managing the potential for maladaptive plasticity, such as neuropathic pain (Bradbury & Burnside, 2019).

Other names
CSPGsLecticansGlial scar ECMChondroitin sulfate glycosaminoglycansCS-GAGsPerineuronal net components
02

Mechanism of action

Therapeutic strategies primarily involve the enzymatic digestion of the inhibitory chondroitin sulfate (CS) glycosaminoglycan (GAG) chains using Chondroitinase ABC, or the pharmacological blockade of CSPG receptors such as Protein Tyrosine Phosphatase sigma (PTPσ) and Leukocyte Common Antigen-Related (LAR) phosphatase to prevent the activation of RhoA-mediated growth cone collapse (Bradbury & Burnside, 2019; Lang et al., 2015).

03

Biological functions

Axon guidanceInhibition of neurite outgrowthCell adhesionSynaptic plasticity regulationStructural support
04

Disease associations

Spinal cord injuryTraumatic brain injuryStrokeMultiple sclerosisNeurodegenerative disease
05

Safety considerations

Off-target degradation of perineuronal netsRisk of neuropathic pain due to aberrant sproutingBlood-brain barrier penetrationImmunogenicity of bacterial enzymes
06

Interacting drugs

Chondroitinase ABC

4 more in the full profile.

07

Biomarkers

Chondroitin sulfate levelsGlial fibrillary acidic protein (GFAP)Neurofilament light chain (NfL)Scar volume (via MRI)

Beyond the preview

Go deeper on Chondroitin sulfate proteoglycan (CSPG) (CSPG).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Chondroitin sulfate proteoglycan (CSPG) (CSPG).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call