Intervertebral disc progenitor cells: roles in regeneration and disease

Intervertebral disc (IVD) degenerative disease is a prevalent and debilitating spinal disease. Current treatments only focus on symptomatic relief but fail to halt disease progression or restore the native biomechanical function of the spine. Regenerative medicine strategies, particularly those harnessing endogenous progenitor cells, offer a promising avenue for achieving biological repair and functional homeostasis. The identification of intervertebral disc progenitor cells (IVD-PCs) has unveiled a potential cellular reservoir for self-repair, given their demonstrated stemness attributes, including clonogenicity and multipotent differentiation. However, the clinical translation of IVD-PCs is significantly hampered by an incomplete understanding of their inherent heterogeneity, hierarchical organization, and, most critically, the dynamic interplay with their unique microenvironment, which dictates their fate decisions. This review synthesizes recent advances in deciphering the molecular signatures and functional plasticity of IVD-PCs. We place a particular emphasis on how key physicochemical, mechanical, and cellular cues within the IVD niche orchestrate progenitor cell behavior-ranging from maintenance and activation to aberrant differentiation-during both homeostasis and degeneration. Furthermore, we propose forward-looking insights to bridge critical knowledge gaps, aiming to propel the development of novel progenitor cell-based therapeutics for IVD degeneration.

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Publication Details

Journal
Stem Cell Research & Therapy
Published
2026-03-15
DOI
https://doi.org/10.1186/s13287-026-04918-5
Primary Topic
Spine and Intervertebral Disc Pathology
Type
article
Field-Weighted Citation Impact
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article

Intervertebral disc progenitor cells: roles in regeneration and disease

P Yan, Ou Hu, Yang Li, Yue Wu et al.
Stem Cell Research & Therapy
Spine and Intervertebral Disc Pathology
article

Intervertebral disc progenitor cells: roles in regeneration and disease

P Yan, Ou Hu, Yang Li, Yue Wu, He Jin, Yingbo Wang, Sha Huang, Ya Huang, Yibo Gan, Jungang Pu, Jian Wu, Peng Lin, Qin Qin, Peng Liu, Yangli Xie, Chen Lin, Sien Lin, Jian He, Lin Chen
article en

Abstract

Intervertebral disc (IVD) degenerative disease is a prevalent and debilitating spinal disease. Current treatments only focus on symptomatic relief but fail to halt disease progression or restore the native biomechanical function of the spine. Regenerative medicine strategies, particularly those harnessing endogenous progenitor cells, offer a promising avenue for achieving biological repair and functional homeostasis. The identification of intervertebral disc progenitor cells (IVD-PCs) has unveiled a potential cellular reservoir for self-repair, given their demonstrated stemness attributes, including clonogenicity and multipotent differentiation. However, the clinical translation of IVD-PCs is significantly hampered by an incomplete understanding of their inherent heterogeneity, hierarchical organization, and, most critically, the dynamic interplay with their unique microenvironment, which dictates their fate decisions. This review synthesizes recent advances in deciphering the molecular signatures and functional plasticity of IVD-PCs. We place a particular emphasis on how key physicochemical, mechanical, and cellular cues within the IVD niche orchestrate progenitor cell behavior-ranging from maintenance and activation to aberrant differentiation-during both homeostasis and degeneration. Furthermore, we propose forward-looking insights to bridge critical knowledge gaps, aiming to propel the development of novel progenitor cell-based therapeutics for IVD degeneration.

Stem Cell Research & Therapy
Army Medical University (CN), Chinese University of Hong Kong (HK), Daping Hospital (CN), Chengdu Military General Hospital (CN), Prince of Wales Hospital (CN), People's Hospital of Bishan District (CN), First People's Hospital of Chongqing (CN)
Openalex Percentile: Top 23%
Spine and Intervertebral Disc Pathology
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