Nitric Oxide-Releasing Bioinspired Scaffold for Exquisite Regeneration of Osteoporotic Bone via Regulation of Homeostasis.
Jun-Kyu LeeDa-Seul KimSo-Yeon ParkSeung-Woon BaekJi-Won JungTae-Hyung KimDong Keun HanPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2022)
Osteoporotic bone regeneration is a challenging process which involves the occurrence of sophisticated interactions. Although various polymeric scaffolds have been proposed for bone repair, research on osteoporotic bone regeneration remains practically limited. In particular, achieving satisfactory bone regeneration when using osteoporotic drugs is challenging including bisphosphonates. Here, a novel nitric oxide-releasing bioinspired scaffold with bioactive agents for the exquisite regeneration of osteoporotic bone is proposed. The bone-like biomimetic poly(lactic-co-glycolic acid) scaffold is first prepared in combination with organic/inorganic ECM and magnesium hydroxide as the base implant material. Nanoparticles containing bioactive agents of zinc oxide (ZO), alendronate, and BMP2 are incorporated to the biomimetic scaffold to impart multifunctionality such as anti-inflammation, angiogenesis, anti-osteoclastogenesis, and bone regeneration. Especially, nitric oxide (NO) generated from ZO stimulates the activity of cGMP and protein kinase G; in addition, ZO downregulates the RANKL/osteoprotegerin ratio by suppressing the Wnt/β-catenin signaling pathway. The new bone is formed much better in the osteoporotic rat model than in the normal model through the regulation of bone homeostasis via the scaffold. These synergistic effects suggest that such a bioinspired scaffold could be a comprehensive way to regenerate exceptionally osteoporotic bones.
Keyphrases
- bone regeneration
- tissue engineering
- nitric oxide
- bone mineral density
- stem cells
- postmenopausal women
- nitric oxide synthase
- body composition
- protein kinase
- oxidative stress
- risk assessment
- cell proliferation
- drug delivery
- endothelial cells
- immune response
- mesenchymal stem cells
- soft tissue
- vascular endothelial growth factor
- drug induced
- lps induced