Mitochondria-engine with self-regulation to restore degenerated intervertebral disc cells via bioenergetic robust hydrogel design.

Bioact Mater

Analytical & Testing Center, Department of Orthopedic Surgery and Orthopedic Research Institute, West China Hospital, Sichuan University, Chengdu, 610065, China.

Published: October 2024

AI Article Synopsis

  • Intervertebral disc degeneration (IDD) is linked to inflammation and decreased mitochondrial membrane potential (MMP), with reactive oxygen species (ROS) playing a significant role in this process.
  • * Researchers proposed a "mitochondrion-engine" system that cools inflammatory environments and restores mitochondrial function, using a composite hydrogel and 3D-printed scaffold to enhance cell energy metabolism.
  • * The system demonstrated improved cell proliferation, collagen synthesis, and mitochondrial activity under oxidative stress, suggesting it could be an effective treatment for IDD.

Article Abstract

Previous studies have confirmed that intervertebral disc degeneration (IDD) is closely associated with inflammation-induced reactive oxygen species (ROS) and resultant cell mitochondrial membrane potential (MMP) decline. Clearance of ROS in an inflammatory environment is essential for breaking the vicious cycle of MMP decline. Additionally, re-energizing the mitochondria damaged in the inflammatory milieu to restore their function, is equally important. Herein, we proposed an interesting concept of mitochondrion-engine equipped with coolant, which enables first to "cool-down" the inflammatory environment, next to restore the MMP, finally to allow cells to regain normal energy metabolism through materials design. As such, we developed a multi-functional composite composed of a reactive oxygen species (ROS)-responsive sodium alginate/gelatin hydrogel infused into a rigid 3D-printed thermoplastic polyurethane (TPU) scaffold. The TPU scaffold was coated with conductive polypyrrole (PPy) to electrophoretically deposit l-arginine, which could upregulate the Mammalian target of rapamycin () pathway, thus increasing MMP and energy metabolism to stimulate extracellular matrix synthesis for IVD repair. While the ROS-responsive hydrogel acting as the "mito-engine coolant" could scavenge the excessive ROS to create a favorable environment for IVD cells recovery. Demonstrated by and evaluations, the mito-engine system markedly promoted the proliferation and collagen synthesis of nucleus pulposus cells while enhancing the mitochondrial respiration and MMP under oxidative stress. Radiological and histological assessments revealed the efficacy of this system in IVD repair. This unique bioinspired design integrated biomaterial science with mitochondrial biology, presents a promising paradigm for IDD treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11167444PMC
http://dx.doi.org/10.1016/j.bioactmat.2024.05.044DOI Listing

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