Related Experiment Video
Updated: May 12, 2026

Optical Sectioning and Visualization of the Intervertebral Disc from Embryonic Development to Degeneration
Published on: July 8, 2021
Characterization of miRNA expression in human degenerative lumbar disks
Søren Ohrt-Nissen1, Kristina B V Døssing, Maria Rossing
1Genomic Medicine, Department of Clinical Biochemistry, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark. ohrtnissen@gmail.com
Background Data:
microRNAs (miRNAs) are short ∼22 nucleotide RNA sequences that regulate messengerRNA translation. miRNAs have shown to play a role in synthesis of inflammatory mediators. Since inflammation play a role in intervertebral disk (IVD) degeneration, the objective was to isolate miRNA from human lumbar intervertebral disks and subsequently characterize the difference in miRNA expression between the annulus fibrosus (AF) and nucleus pulposus (NP).
Methods:
Fourteen patients undergoing anterior interbody fusion for degenerative disk disease of the lumbar spine were included. During surgery biopsies from the intervertebral disks were obtained and immediately placed in RNAlater. The RNAlater was decanted and the samples frozen at -80˚C until RNA extraction. This was performed using the Trizol method. Global miRNA expression analysis was performed using the Affymetrix GeneChip® miRNA array.
Results:
We developed a method allowing the extraction of miRNA from human intervertebral disks usually yielding 1-4 µg of total RNA pr. 100 mg of disk. Twenty-seven miRNAs had a higher expression in the AF and 10 had the highest expression in the NP. Among the top 15 signaling pathways most likely to be controlled by these miRNAs were the transforming growth factor β (TGFβ), platelet-derived growth factor (PDGF), insulin-like growth factor (IGF) epidermal growth factor (EGF), and actin cytoskeletal pathway.
Conclusion:
We have demonstrated the presence of miRNA in the human IVD. The miRNA expression differs from muscle tissue and there are differences between the miRNA expressed in the NP and AF. The miRNAs identified control signaling pathways important for maintenance of the IVD. Future studies may determine the importance of miRNA in the development of IVD disease.
Insights
microRNAs (miRNAs) are present in human intervertebral discs (IVDs). Their expression differs between the nucleus pulposus and annulus fibrosus, impacting key signaling pathways involved in IVD health.
Area of Science:
- Molecular Biology
- Biochemistry
- Genetics
Background:
- MicroRNAs (miRNAs) are short RNA sequences regulating gene expression.
- Inflammation is implicated in intervertebral disc (IVD) degeneration.
- Understanding miRNA roles in IVD is crucial for degenerative disc disease research.
Purpose of the Study:
- To isolate and characterize microRNAs (miRNAs) from human lumbar intervertebral discs (IVDs).
- To compare miRNA expression profiles between the annulus fibrosus (AF) and nucleus pulposus (NP) of human IVDs.
- To identify signaling pathways regulated by differentially expressed miRNAs in IVDs.
Main Methods:
- RNA extraction from human lumbar IVD biopsies using the Trizol method.
- Global miRNA expression profiling via Affymetrix GeneChip® miRNA array.
- Analysis of miRNA expression differences between AF and NP tissues.
Main Results:
- Successful isolation of miRNA from human IVDs, yielding 1-4 µg of total RNA per 100 mg of tissue.
- Twenty-seven miRNAs showed higher expression in AF, while 10 showed higher expression in NP.
- Identified key signaling pathways regulated by these miRNAs, including TGFβ, PDGF, IGF, EGF, and actin cytoskeletal pathways.
Conclusions:
- Confirmed the presence of miRNAs in human IVDs.
- Demonstrated distinct miRNA expression patterns in NP and AF compared to muscle tissue.
- Highlighted the role of identified miRNAs in regulating critical signaling pathways for IVD maintenance, suggesting potential involvement in IVD disease pathogenesis.
Related Concept Videos
Degenerative Disc Disease I: Introduction
Degenerative Disc Disease ll: Pathophysiology
MicroRNAs
MicroRNAs
Herniated Intervertebral Disc l: Introduction

