Autophagy in the Degenerating Human Intervertebral Disc: In Vivo Molecular and Morphological Evidence, and Induction of Autophagy in Cultured Annulus Cells Exposed to Proinflammatory Cytokines—Implications for Disc Degeneration. Issue 11 (1st June 2015)

• Record Type: Journal Article
• Authors: Gruber, Helen E.; Hoelscher, Gretchen L.; Ingram, Jane A.; Bethea, Synthia; Hanley, Edward N.
• Is Part Of: Spine. Volume 40:Issue 11(2015)
• Publication Date: 2015-06-01
• Subjects: intervertebral disc -- autophagy -- p62/SQSTM1 -- IL-1β -- PIM-2 oncogene -- WIPI49 -- TNF-α -- proinflammatory cytokines -- disc degeneration; Spine -- Abnormalities -- Periodicals; Spine -- Diseases -- Periodicals; Spine -- Surgery -- Periodicals; 616.73005
• DOI: 10.1097/BRS.0000000000000865
• Languages: English
• ISSNs: 0362-2436

Abstract

Abstract : Study Design: Autophagy-related gene expression and ultrastructural features of autophagy were studied in human discs. Objective: To obtain molecular/morphological data on autophagy in human disc degeneration and cultured human annulus cells exposed to proinflammatory cytokines. Summary of Background Data: Autophagy is an important process by which cytoplasm and organelles are degraded; this adaptive response to sublethal stresses (such as nutrient deprivation present in disc degeneration) supplies needed metabolites. Little is known about autophagic processes during disc degeneration. Methods: Human disc specimens were obtained after institutional review board approval. Annulus mRNA was analyzed to determine autophagy-related gene expression levels. Immunolocalization and ultrastructural studies for p62, ATG3, ATG4B, ATG4C, ATG7, L3A, ULK-2, and beclin were conducted. In vitro experiments used IL-1β- or TNF-α–treated human annulus cells to test for autophagy-related gene expression. Results: More degenerated versus healthier discs showed significantly greater upregulation of well-recognized autophagy-related genes ( P ⩽ 0.028): beclin 1 (upregulated 1.6-fold); ATG8 (LC3) (upregulated 2.0-fold); ATG12 (upregulated 4.0-fold); presenilin 1 (upregulated 1.6-fold); cathepsin B (upregulated 4.5-fold). p62 was localized, and ultrastructure showed autophagic vacuolization and autophagosomes with complex, redundant whorls of membrane-derived material. In vitro, proinflammatory cytokines significantly upregulated autophagy-related genes ( P ⩽ 0.04): DRAM1 (6.24-fold); p62 (4.98-fold); PIM-2 oncogene, a positive regulator of autophagy (3-fold); WIPI49 (linked to starvation-induced autophagy) (upregulated 2.3-fold). Conclusion: Data provide initial molecular and morphological evidence for the presence of autophagy in the degenerating human annulus. In vivo gene analyses showed greater autophagy-related gene expression in more degenerated than healthier discs. In vitro data suggested a mechanism implicating a role of TNF-α and IL-1β in disc autophagy. Findings suggest the importance of future work to investigate the relationship of autophagy to apoptosis, cell death, cell senescence, and mitochondrial dysfunction in the aging and degenerating disc. Level of Evidence: N/A Abstract : More degenerated versus less degenerated discs showed greater upregulation of autophagy-related genes (beclin 1, ATG8, ATG12, presenilin 1, and cathepsin B). Proinflammatory cytokine exposure in vitro upregulated autophagy-related genes (DRAM1, p62, and PIM-2 oncogene). Data stress the need for increased understanding of autophagy in disc cell biology and disc degeneration.