Raphanus sativus Linne Protects Human Nucleus Pulposus Cells against H2O2-Induced Damage by Inhibiting TREM2

Intervertebral disc degeneration (IDD) progresses owing to damage and depletion of nucleus pulposus (NP) cells. Cytoprotection mitigates oxidative stress, nutrient deprivation, and mechanical stress, which lead to cell damage and necrosis. We aimed to examine the protective effect of <i>Raphanus sativus</i> Linne (RSL), common radish, against oxidative stress by H<sub>2</sub>O<sub>2</sub> in human NP cells and whether the RSL extracts can inhibit triggering receptor expressed on myeloid cells 2 (TREM2), an inducer of apoptosis and degeneration in NP cells. We administered hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) to cultured human NP cells treated with RSL extracts. We used immunoblotting and quantitative PCR to investigate expression of the apoptosis-associated proteins in cultured cells. RSL significantly enhanced cell survival by suppressing the activation of cleaved caspase-3 and Bax. In contrast, RSL extract increased Bcl2 concentration to downregulate apoptosis. Additionally, RSL treatment notably enhanced the mRNA levels of <i>ACAN</i> and <i>Col2a1</i> while significantly reducing those of <i>ADAMTS-4</i>, <i>ADAMTS-5</i>, <i>MMP3</i>, and <i>MMP13</i>, key genes involved in NP degeneration. While H<sub>2</sub>O<sub>2</sub> elevated TREM2 expression, causing disc degeneration, RSL downregulated TREM2 expression. Thus, our findings imply that RSL supports human NP cells under oxidative stress and regulates the pathways underlying disc degeneration, particularly TREM2, and that RSL extracts may potentially prevent IDD.

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Publication Details

Journal
Biology
Published
2024-08-09
DOI
https://doi.org/10.3390/biology13080602
Citations
1
Primary Topic
Spine and Intervertebral Disc Pathology
Type
article
Field-Weighted Citation Impact
0.42

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article

Raphanus sativus Linne Protects Human Nucleus Pulposus Cells against H2O2-Induced Damage by Inhibiting TREM2

Seung Ho Baek, Yoon Jae Lee, In‐Hyuk Ha, Hyun Sil Kim et al.
1 citations
Biology
Spine and Intervertebral Disc Pathology
0.42
article

Raphanus sativus Linne Protects Human Nucleus Pulposus Cells against H2O2-Induced Damage by Inhibiting TREM2

Seung Ho Baek, Yoon Jae Lee, In‐Hyuk Ha, Hyun Sil Kim, Wan‐Jin Jeon, Changhwan Yeo, Junseon Lee, Jin Young Hong, Hyunseong Kim
article en
1 citations

Abstract

Intervertebral disc degeneration (IDD) progresses owing to damage and depletion of nucleus pulposus (NP) cells. Cytoprotection mitigates oxidative stress, nutrient deprivation, and mechanical stress, which lead to cell damage and necrosis. We aimed to examine the protective effect of <i>Raphanus sativus</i> Linne (RSL), common radish, against oxidative stress by H<sub>2</sub>O<sub>2</sub> in human NP cells and whether the RSL extracts can inhibit triggering receptor expressed on myeloid cells 2 (TREM2), an inducer of apoptosis and degeneration in NP cells. We administered hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) to cultured human NP cells treated with RSL extracts. We used immunoblotting and quantitative PCR to investigate expression of the apoptosis-associated proteins in cultured cells. RSL significantly enhanced cell survival by suppressing the activation of cleaved caspase-3 and Bax. In contrast, RSL extract increased Bcl2 concentration to downregulate apoptosis. Additionally, RSL treatment notably enhanced the mRNA levels of <i>ACAN</i> and <i>Col2a1</i> while significantly reducing those of <i>ADAMTS-4</i>, <i>ADAMTS-5</i>, <i>MMP3</i>, and <i>MMP13</i>, key genes involved in NP degeneration. While H<sub>2</sub>O<sub>2</sub> elevated TREM2 expression, causing disc degeneration, RSL downregulated TREM2 expression. Thus, our findings imply that RSL supports human NP cells under oxidative stress and regulates the pathways underlying disc degeneration, particularly TREM2, and that RSL extracts may potentially prevent IDD.

BiologyVol. 13(8)
Dongguk University (KR), Jaseng Medical Foundation (KR)
Korea Health Industry Development Institute
Openalex Percentile: Top 36%
Spine and Intervertebral Disc Pathology
0.42
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