An enzyme-proof glycan glue for extracellular matrix to ameliorate intervertebral disc degeneration

Intervertebral disc degeneration (IDD) remains a global healthcare challenge. Here, by analyzing clinical samples, we discover the loss of milk fat globule-EGF factor 8 (MFG-E8) from the nucleus pulposus (NP) tissue-along with increased enzymatic breakdown of glycosaminoglycans (GAGs)-as an overlooked factor for IDD development. Repairing the degraded NP extracellular matrix (ECM) with a structurally-mimicking glycan glue to enrich MFG-E8 may counter the degeneration. Accordingly, we synthesize a glucomannan octanoate (GMOC) with robust resistance to ECM-cleaving enzymes, which forms assemblies with MFG-E8 to maintain a healthy NP cell phenotype. GMOC injected into the degenerated intervertebral disc enriches MFG-E8 in situ, leading to NP tissue regeneration in a rat and a rabbit model, which represent two clinical scenarios of pre-surgical intervention and post-surgical regeneration of IDD, respectively. In summary, we report enriching MFG-E8 in ECM with a glycan glue as a mechanism to promote NP regeneration for IDD treatment.

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Publication Details

Journal
Nature Communications
Published
2025-04-16
DOI
https://doi.org/10.1038/s41467-025-58946-5
Citations
5
Primary Topic
Spine and Intervertebral Disc Pathology
Type
article
Field-Weighted Citation Impact
7.36
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An enzyme-proof glycan glue for extracellular matrix to ameliorate intervertebral disc degeneration

Dechun Geng, Lei Dong, Tzuwei Chao, Yuwei Li et al.
5 citations
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Spine and Intervertebral Disc Pathology
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article

An enzyme-proof glycan glue for extracellular matrix to ameliorate intervertebral disc degeneration

Dechun Geng, Lei Dong, Tzuwei Chao, Yuwei Li, Peng Peng, Chunming Wang, Gaoran Ge, Yu Liu
article en
5 citations

Abstract

Intervertebral disc degeneration (IDD) remains a global healthcare challenge. Here, by analyzing clinical samples, we discover the loss of milk fat globule-EGF factor 8 (MFG-E8) from the nucleus pulposus (NP) tissue-along with increased enzymatic breakdown of glycosaminoglycans (GAGs)-as an overlooked factor for IDD development. Repairing the degraded NP extracellular matrix (ECM) with a structurally-mimicking glycan glue to enrich MFG-E8 may counter the degeneration. Accordingly, we synthesize a glucomannan octanoate (GMOC) with robust resistance to ECM-cleaving enzymes, which forms assemblies with MFG-E8 to maintain a healthy NP cell phenotype. GMOC injected into the degenerated intervertebral disc enriches MFG-E8 in situ, leading to NP tissue regeneration in a rat and a rabbit model, which represent two clinical scenarios of pre-surgical intervention and post-surgical regeneration of IDD, respectively. In summary, we report enriching MFG-E8 in ECM with a glycan glue as a mechanism to promote NP regeneration for IDD treatment.

Nature CommunicationsVol. 16(1)
China Pharmaceutical University (CN), University of Macau (MO), Soochow University (CN), First Affiliated Hospital of Soochow University (CN), The Synergetic Innovation Center for Advanced Materials (CN), Zhuhai Institute of Advanced Technology (CN), Nanjing University (CN)
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Openalex Percentile: Top 3%
Spine and Intervertebral Disc Pathology
7.36
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