AI Article Synopsis

  • * A new thermosensitive injectable hydrogel (adEHG), made from gallic acid-modified hydroxybutyl chitosan and soluble extracellular matrix, enhances stem cell viability and function by mimicking their natural environment while protecting against oxidative stress.
  • * The adEHG hydrogel not only promotes important processes like angiogenesis and collagen deposition but also aids in wound healing by encouraging beneficial macrophage behavior, improving the prospects for using stem cell therapies in treating pressure ulcers.

Article Abstract

Pressure ulcers are a common issue in elderly and medically compromised individuals, posing significant challenges in healthcare. Human umbilical cord mesenchymal stem cells (HUMSCs) offer therapeutic benefits like inflammation modulation and tissue regeneration, yet challenges in cell survival, retention, and implantation rates limit their clinical application. Hydrogels in three-dimensional (3D) stem cell culture mimic the microenvironment, improving cell survival and therapeutic efficacy. A thermosensitive injectable hydrogel (adEHG) combining gallic acid-modified hydroxybutyl chitosan (HBC-GA) with soluble extracellular matrix (adECM) has been developed to address these challenges. The hybrid hydrogel, with favorable physical and chemical properties, shields stem cells from oxidative stress and boosts their therapeutic potential by clearing ROS. The adEHG hydrogel promotes angiogenesis, cell proliferation, and collagen deposition, further enhancing inflammation modulation and wound healing through the sustained release of therapeutic factors and cells. Additionally, the adEHG@HUMSC composite induces macrophage polarization towards an M2 phenotype, which is crucial for wound inflammation inhibition and successful healing. Our research significantly propels the field of stem cell-based therapies for pressure ulcer treatment and underscores the potential of the adEHG hydrogel as a valuable tool in advancing regenerative medicine.

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Source
http://dx.doi.org/10.1016/j.biomaterials.2024.122880DOI Listing

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