Journal
MATRIX BIOLOGY
Volume 94, Issue -, Pages 110-133Publisher
ELSEVIER
DOI: 10.1016/j.matbio.2020.09.003
Keywords
Intervertebral disc degeneration; Extracellular matrix; Sox9; Mouse model; Nucleus pulposus; Annulus fibrosus
Categories
Funding
- NIH/NIAMS [R01 AR055655, AR064733, AR074813, AR072649, T32 AR052273]
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SOX9 plays an important role in chondrocyte differentiation and, in the developing axial skeleton, maintains the notochord and the demarcation of intervertebral disc compartments. Diminished expression is linked to campomelic dysplasia, resulting in severe scoliosis and progressive disc degeneration. However, the specific functions of SOX9 in the adult spinal column and disc are largely unknown. Accordingly, employing a strategy to conditionally delete Sox9 in Acan-expressing cells (Acan(CreERT2)Sox9(fl/fl)), we delineated these functions in the adult intervertebral disc. Acan(CreERT2)Sox9(fl/fl) mice (Sox9(cKO)) showed extensive and progressive remodeling of the extracellular matrix in nucleus pulposus (NP) and annulus fibrosus (AF), consistent with human disc degeneration. Progressive degeneration of the cartilaginous endplates (EP) was also evident in Sox9(cKO) mice, and it preceded morphological changes seen in the NP and AF compartments. Fate mapping using tdTomato reporter, EdU chase, and quantitative immunohistological studies demonstrated that SOX9 is crucial for disc cell survival and phenotype maintenance. Microarray analysis showed that Sox9 regulated distinct compartment-specific transcriptomic landscapes, with prominent contributions to the ECM, cytoskeleton-related, and metabolic pathways in the NP and ion transport, the cell cycle, and signaling pathways in the AF. In summary, our work provides new insights into disc degeneration in Sox9(cKO) mice at the cellular, molecular, and transcriptional levels, underscoring tissue-specific roles of this transcription factor. Our findings may direct future cell therapies targeting SOX9 to mitigate disc degeneration. (C) 2020 Elsevier B.V. All rights reserved.
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