Skip to content

Bimetallic modified titanium carbide nanoparticles loaded with transcription factor E3 ameliorate intervertebral disc degeneration by eliminating reactive oxygen species and promoting autophagic flux.

Aug 2026 · International Journal of Biological Macromolecules · pp. 153997 · 0 citations · 36 references
Medicine

TL;DR

In a needle puncture-induced IVDD rat model, intra-disc injection of Ti3C2@PtAu@TFE3 alleviated structural deterioration and prevented ECM destruction and the potential application of Ti3C2@PtAu@TFE3 against IVDD is demonstrated.

Abstract

Intervertebral disc (IVD) degeneration (IVDD) is a major cause of lower back pain, characterized by oxidative stress accumulation and impaired autophagic flux leading to nucleus pulposus cell (NPC) degeneration. Transcription factor E3 (TFE3) is crucial in autophagy regulation. MXene, a nanomaterial known for its antioxidant capability, exhibits satisfactory therapeutic effects in various diseases. This study investigates the role of TFE3 and evaluates the therapeutic potential of Ti3C2 MXene-based nanocomposites in IVDD. The Ti3C2@PtAu@TFE3 nanocomposite was designed, with properties of anti-oxidation and pro-autophagic flux, alleviated extracellular matrix (ECM) degradation and senescence in NPCs. In a needle puncture-induced IVDD rat model, intra-disc injection of Ti3C2@PtAu@TFE3 alleviated structural deterioration and prevented ECM destruction. This study highlights the critical role of TFE3 in IVDD pathogenesis and demonstrates the potential application of Ti3C2@PtAu@TFE3 against IVDD.

View source

Similar papers

Jul 2026

Nanozyme-integrated hydrogel orchestrates mitochondrial quality control to counter inflammatory and oxidative milieu during disc degeneration.

In vitro and in vivo evidence confirms that this dual-functional hydrogel attenuates NP cell inflammation and significantly retards the progression of IDD, offering a synergistic strategy that couples nanozyme-mediated antioxidant therapy with targeted FPR1 blockade, holding substantial promise for intervertebral disc...

Zhiwei Liao, Guoqiang Yin, Jing-Pei Liu et al. · 0 citations
Jul 2026

A multifunctional injectable hydrogel co-delivering GDF6 and MnO2 nanozymes alleviates intervertebral disc degeneration by mitigating oxidative stress and promoting anabolic repair.

It is demonstrated that the multifunctional Gel@MnO2/GDF6 hydrogel effectively promotes intervertebral disc regeneration by concurrently mitigating oxidative stress and fostering an anabolic, anti-inflammatory microenvironment, validating its potential as a promising therapeutic method for IDD.

Chao Wei, Qin Tang, Yanlin Tan et al. · 0 citations
Aug 2026

Thonningianin a mitigates intervertebral disc degeneration by inhibiting ferroptosis via chelating Fe2+ and regulating the adenosine monophosphate-activated protein kinase (AMPK)/ nuclear factor erythroid 2-related factor 2 (Nrf2)/ glutathione peroxidase 4 (GPX4) pathway.

BACKGROUND Oxidative stress and ferroptosis play critical roles in the pathogenesis of intervertebral disc degeneration (IVDD). Thonningianin A (TA) is a complex polyphenolic ellagitannin found in plants like Thonningia sanguinea, and it exhibits free radical scavenging, anti-superoxide anion generation and metal-chela...

Ye-Kai Zhang, Jiawei Qiu, Han-Wen Zhang et al. · 0 citations
Jul 2026

The USP5-MATN3 axis in nucleus pulposus cell senescence: A Deubiquitination mechanism protecting against intervertebral disc degeneration.

This study clarifies the molecular mechanism by which the USP5/MATN3 axis regulates cellular senescence and affects IVDD progression, opening up new potential targets for the intervention strategy of IVDD.

Chunyang Fan, Jie-yun Xia, Yao Zhang et al. · 0 citations
Jul 2026

Youthful-state extracellular vesicles for targeted therapy of intervertebral disc degeneration: resolving inflammation and pyroptosis through NF-κB suppression and NLRP1 inactivation

It is demonstrated that youthful-state EVs (Y-EVs) outperform aged donor-derived EVs (O-EVs) in resolving inflammatory cascades within nucleus pulposus (NP) cells and establishes CD55 as a key determinant of their therapeutic superiority.

Zhi-Wei Liao, Kun Wang, M. Lei et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.