Chondroitin-4-sulfation negatively regulates axonal guidance and growth

Author:

Wang Hang1,Katagiri Yasuhiro1,McCann Thomas E.1,Unsworth Edward2,Goldsmith Paul2,Yu Zu-Xi3,Tan Fei1,Santiago Lizzie1,Mills Edward M.4,Wang Yu5,Symes Aviva J.5,Geller Herbert M.1

Affiliation:

1. Developmental Neurobiology Section, National Institutes of Health, Bethesda, MD 20892, USA

2. Basic Research Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA

3. Pathology Core, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA

4. Division of Pharmacology/Toxicology, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA

5. Department of Pharmacology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA

Abstract

Glycosaminoglycan (GAG) side chains endow extracellular matrix proteoglycans with diversity and complexity based upon the length, composition and charge distribution of the polysaccharide chain. Using cultured primary neurons, we show that specific sulfation in the GAG chains of chondroitin sulfate mediates neuronal guidance cues and axonal growth inhibition. Chondroitin-4-sulfate (CS-A), but not chondroitin-6-sulfate (CS-C), exhibits a strong negative guidance cue to mouse cerebellar granule neurons. Enzymatic and gene-based manipulations of 4-sulfation in the GAG side chains alter their ability to direct growing axons. Furthermore, 4-sulfated chondroitin sulfate GAG chains are rapidly and significantly increased in regions that do not support axonal regeneration proximal to spinal cord lesions in mice. Thus, our findings show that specific sulfation along the carbohydrate backbone carries instructions to regulate neuronal function.

Publisher

The Company of Biologists

Subject

Cell Biology

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