Loss of HIF-1α in the notochord results in cell death and complete disappearance of the nucleus pulposus

Christophe Merceron, Laura Mangiavini, Alexander Robling, Tremika Leshan Wilson, Amato J. Giaccia, Irving M. Shapiro, Ernestina Schipani, Makarand V. Risbud

Research output: Contribution to journalArticle

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Abstract

The intervertebral disc (IVD) is one of the largest avascular organs in vertebrates. The nucleus pulposus (NP), a highly hydrated and proteoglycan-enriched tissue, forms the inner portion of the IVD. The NP is surrounded by a multi-lamellar fibrocartilaginous structure, the annulus fibrosus (AF). This structure is covered superior and inferior side by cartilaginous endplates (CEP). The NP is a unique tissue within the IVD as it results from the differentiation of notochordal cells, whereas, AF and CEP derive from the sclerotome. The hypoxia inducible factor-1a (HIF-1a) is expressed in NP cells but its function in NP development and homeostasis is largely unknown. We thus conditionally deleted HIF-1α in notochordal cells and investigated how loss of this transcription factor impacts NP formation and homeostasis at E15.5, birth, 1 and 4 months of age, respectively. Histological analysis, cell lineage studies, and TUNEL assay were performed. Morphologic changes of the mutant NP cells were identified as early as E15.5, followed, postnatally, by the progressive disappearance and replacement of the NP with a novel tissue that resembles fibrocartilage. Notably, lineage studies and TUNEL assay unequivocally proved that NP cells did not transdifferentiate into chondrocyte-like cells but they rather underwent massive cell death, and were completely replaced by a cell population belonging to a lineage distinct from the notochordal one. Finally, to evaluate the functional consequences of HIF-1α deletion in the NP, biomechanical testing of mutant IVD was performed. Loss of the NP in mutant mice significantly reduced the IVD biomechanical properties by decreasing its ability to absorb mechanical stress. These findings are similar to the changes usually observed during human IVD degeneration. Our study thus demonstrates that HIF-1α is essential for NP development and homeostasis, and it raises the intriguing possibility that this transcription factor could be involved in IVD degeneration in humans.

Original languageEnglish (US)
Article numberA1852
JournalPLoS One
Volume9
Issue number10
DOIs
StatePublished - Oct 22 2014

Fingerprint

Notochord
intervertebral disks
Cell death
cell death
Cell Death
Tissue
Assays
Transcription Factors
Cells
Intervertebral Disc
cell nucleus
Lamellar structures
homeostasis
Proteoglycans
mutants
transcription factors
Intervertebral Disc Degeneration
cells
Homeostasis
In Situ Nick-End Labeling

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Merceron, C., Mangiavini, L., Robling, A., Wilson, T. L., Giaccia, A. J., Shapiro, I. M., ... Risbud, M. V. (2014). Loss of HIF-1α in the notochord results in cell death and complete disappearance of the nucleus pulposus. PLoS One, 9(10), [A1852]. https://doi.org/10.1371/journal.pone.0110768

Loss of HIF-1α in the notochord results in cell death and complete disappearance of the nucleus pulposus. / Merceron, Christophe; Mangiavini, Laura; Robling, Alexander; Wilson, Tremika Leshan; Giaccia, Amato J.; Shapiro, Irving M.; Schipani, Ernestina; Risbud, Makarand V.

In: PLoS One, Vol. 9, No. 10, A1852, 22.10.2014.

Research output: Contribution to journalArticle

Merceron, C, Mangiavini, L, Robling, A, Wilson, TL, Giaccia, AJ, Shapiro, IM, Schipani, E & Risbud, MV 2014, 'Loss of HIF-1α in the notochord results in cell death and complete disappearance of the nucleus pulposus', PLoS One, vol. 9, no. 10, A1852. https://doi.org/10.1371/journal.pone.0110768
Merceron, Christophe ; Mangiavini, Laura ; Robling, Alexander ; Wilson, Tremika Leshan ; Giaccia, Amato J. ; Shapiro, Irving M. ; Schipani, Ernestina ; Risbud, Makarand V. / Loss of HIF-1α in the notochord results in cell death and complete disappearance of the nucleus pulposus. In: PLoS One. 2014 ; Vol. 9, No. 10.
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