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Hydrogen Sulfide Delivery to Enhance Bone Tissue Engineering Cell Survival.
- Source :
- Pharmaceuticals (14248247); May2024, Vol. 17 Issue 5, p585, 16p
- Publication Year :
- 2024
-
Abstract
- Though crucial for natural bone healing, local calcium ion (Ca<superscript>2+</superscript>) and phosphate ion (P<subscript>i</subscript>) concentrations can exceed the cytotoxic limit leading to mitochondrial overload, oxidative stress, and cell death. For bone tissue engineering applications, H<subscript>2</subscript>S can be employed as a cytoprotective molecule to enhance mesenchymal stem cell (MSC) tolerance to cytotoxic Ca<superscript>2+</superscript>/P<subscript>i</subscript> concentrations. Varied concentrations of sodium hydrogen sulfide (NaSH), a fast-releasing H<subscript>2</subscript>S donor, were applied to assess the influence of H<subscript>2</subscript>S on MSC proliferation. The results suggested a toxicity limit of 4 mM for NaSH and that 1 mM of NaSH could improve cell proliferation and differentiation in the presence of cytotoxic levels of Ca<superscript>2+</superscript> (32 mM) and/or P<subscript>i</subscript> (16 mM). To controllably deliver H<subscript>2</subscript>S over time, a novel donor molecule (thioglutamic acid—GluSH) was synthesized and evaluated for its H<subscript>2</subscript>S release profile. Excitingly, GluSH successfully maintained cytoprotective level of H<subscript>2</subscript>S over 7 days. Furthermore, MSCs exposed to cytotoxic Ca<superscript>2+</superscript>/P<subscript>i</subscript> concentrations in the presence of GluSH were able to thrive and differentiate into osteoblasts. These findings suggest that the incorporation of a sustained H<subscript>2</subscript>S donor such as GluSH into CaP-based bone graft substitutes can facilitate considerable cytoprotection, making it an attractive option for complex bone regenerative engineering applications. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 14248247
- Volume :
- 17
- Issue :
- 5
- Database :
- Complementary Index
- Journal :
- Pharmaceuticals (14248247)
- Publication Type :
- Academic Journal
- Accession number :
- 177491889
- Full Text :
- https://doi.org/10.3390/ph17050585