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Updated: Jan 25, 2026

Optical Sectioning and Visualization of the Intervertebral Disc from Embryonic Development to Degeneration
Published on: July 8, 2021
Rab7 delays intervertebral disc degeneration through the inhibition of the p38MAPK pathway
Xu Chen1, Peng Zhang2, Xun Ma1
1Department of Orthopedics, Shanxi Dayi Hospital Affiliated to Shanxi Medical University, Taiyuan, 030000, China.
Abstract:
The objective of this study is to determine whether Rab7 could delay intervertebral disc degeneration and study the mechanism. We chose old mice to established intervertebral disc degeneration model and study the effect of Rab7 on intervertebral disc by western blotting, quantitative real-time PCR, immunohistochemistry et al. Nucleus pulposus cells were cultured to study the exact mechanism. Expression of Rab7 was decreased in degenerative human nucleus pulposus tissues. With the aging of mice, the degree of intervertebral disc degeneration was aggravated and the expression of Rab7 was decreased. In addition, overexpression of Rab7 can reduce the degeneration of nucleus pulposus cells and reduce the levels of p38 and p-p38. Rab7 is a protective factor for intervertebral discs and could delays intervertebral disc degeneration through the inhibition of the p38MAPK pathway.
Insights
Rab7 protein protects against intervertebral disc degeneration. Overexpressing Rab7 in nucleus pulposus cells inhibits the p38MAPK pathway, delaying degeneration.
Area of Science:
- Biomedical research
- Cell biology
- Orthopedics
Background:
- Intervertebral disc degeneration (IVDD) is a significant cause of low back pain.
- The molecular mechanisms underlying IVDD progression remain incompletely understood.
- Rab7, a small GTPase, has emerging roles in cellular processes relevant to degeneration.
Purpose of the Study:
- To investigate the role of Rab7 in delaying intervertebral disc degeneration (IVDD).
- To elucidate the underlying molecular mechanism of Rab7's action in nucleus pulposus cells.
Main Methods:
- Established an intervertebral disc degeneration model in aged mice.
- Utilized western blotting, quantitative real-time PCR, and immunohistochemistry.
- Cultured primary nucleus pulposus cells for mechanistic studies.
Main Results:
- Rab7 expression was significantly decreased in degenerative human nucleus pulposus tissues.
- Aging in mice correlated with aggravated IVDD and reduced Rab7 expression.
- Overexpression of Rab7 reduced nucleus pulposus cell degeneration and inhibited p38 and p-p38 levels.
Conclusions:
- Rab7 acts as a protective factor against intervertebral disc degeneration.
- Rab7 delays IVDD by inhibiting the p38MAPK signaling pathway.
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