Inflammaging determines health and disease in lumbar discs: evidence from differing proteomic signatures of healthy, aging and degenerating discs

Abstract

BACKGROUND CONTEXT The true understanding of aging and disc degeneration (DD) is still elusive. MRI has not helped our attempts to understand the health and disease status of the discs as it reflects mainly the end morphological changes and not the changes at a molecular level. Understanding degeneration at a molecular level through proteomics might allow differentiation from normal aging and also aid in the development of biomarkers for early diagnosis and preventive therapies. PURPOSE To utilize proteomics to understand the molecular basis of healthy, aging and degenerating discs and conclusively differentiate normal aging and degeneration. STUDY DESIGN Proteomic analysis of human intervertebral disc samples. METHODS L4-L5 disc samples from three groups were acquired and subjected to proteomic analysis. Samples from individuals aged in the 2nd, 3rd, and 4th decades were used to represent young healthy discs (Group A). Those from MRI normal donors aged in the 5th, 6th and 7th decades represented normal aging (Group B). Five degenerated discs obtained from patients at surgery represented degeneration (Group C). The entire proteome map and alteration in protein expressions were further analyzed using bioinformatics analysis. This was a self-funded project. RESULTS There were 84 common proteins. Specific proteins numbered 225 in A, 315 in B and 283 in C. By gene ontology biological process identification, Group A predominated with extracellular matrix organization, cytoskeletal structural and normal metabolic proteins. Group B differed in having additional basal expression of immune response, complement inhibitors and senescence proteins. Group C was different, with up regulation of proteins associated with oxidative stress response, positive regulators of apoptosis, innate immune response, complement activation and defense response to gram positive bacteria indicating ongoing inflammaging. CONCLUSIONS Our study documented diverse proteome signatures between the young, aging and degenerating discs. Inflammaging was the main differentiation between normal biological aging and DD. CLINICAL SIGNIFICANCE Multiple inflammatory molecules unique to DD were identified, allowing the possibility of developing specific biomarkers for early diagnosis and thereby provide evidence-based metrics for preventive measures rather than surgical intervention and also to monitor progress of the disease. FDA DEVICE/DRUG STATUS This abstract does not discuss or include any applicable devices or drugs. The true understanding of aging and disc degeneration (DD) is still elusive. MRI has not helped our attempts to understand the health and disease status of the discs as it reflects mainly the end morphological changes and not the changes at a molecular level. Understanding degeneration at a molecular level through proteomics might allow differentiation from normal aging and also aid in the development of biomarkers for early diagnosis and preventive therapies. To utilize proteomics to understand the molecular basis of healthy, aging and degenerating discs and conclusively differentiate normal aging and degeneration. Proteomic analysis of human intervertebral disc samples. L4-L5 disc samples from three groups were acquired and subjected to proteomic analysis. Samples from individuals aged in the 2nd, 3rd, and 4th decades were used to represent young healthy discs (Group A). Those from MRI normal donors aged in the 5th, 6th and 7th decades represented normal aging (Group B). Five degenerated discs obtained from patients at surgery represented degeneration (Group C). The entire proteome map and alteration in protein expressions were further analyzed using bioinformatics analysis. This was a self-funded project. There were 84 common proteins. Specific proteins numbered 225 in A, 315 in B and 283 in C. By gene ontology biological process identification, Group A predominated with extracellular matrix organization, cytoskeletal structural and normal metabolic proteins. Group B differed in having additional basal expression of immune response, complement inhibitors and senescence proteins. Group C was different, with up regulation of proteins associated with oxidative stress response, positive regulators of apoptosis, innate immune response, complement activation and defense response to gram positive bacteria indicating ongoing inflammaging. Our study documented diverse proteome signatures between the young, aging and degenerating discs. Inflammaging was the main differentiation between normal biological aging and DD.