Electrosprayed Regeneration-Enhancer-Element Microspheres Power Osteogenesis and Angiogenesis Coupling.
Tianpeng XuYuhe YangDi SuoHo Pan BeiXiaoxiao XuXin ZhaoPublished in: Small (Weinheim an der Bergstrasse, Germany) (2022)
Electrosprayed microspheres for bone regeneration are conventionally restricted by the lack of osteogenic modulation for both encapsulated stem cells and surrounding cells at the defect site. Here, sodium alginate microspheres encapsulating L-arginine doped hydroxyapatite nanoparticles (Arg/HA NPs) and bone mesenchymal stem cells (BMSCs) as regeneration-enhancer-element reservoirs (Arg/HA-SA@BMSC) for bone healing are electrosprayed. The Arg/HA NPs serve as a container of L-arginine and Ca 2+ and the BMSCs inside the microspheres metabolize the released L-arginine into bioactive gas nitric oxide (NO) in the presence of Ca 2+ to activate the nitric oxide (NO)/cyclic guanosine monophosphate (cGMP) signaling pathway. Meanwhile, the generated NO diffuses out of the microspheres together with the Ca 2+ and L-arginine as exterior enhancers to promote the osteogenesis-angiogenesis coupling of surrounding BMSCs and endothelial cells (ECs) at the bone defect site, generating an internal/external modulation loop between the encapsulated cells and surrounding native cells. It is demonstrated that such regeneration-enhancer-element reservoirs could effectively increase the bone tissue formation and neovasculature using rat calvarial defect models. It is envisioned that the microsphere system could streamline vascularized bone regeneration therapy as a high throughput, minimally invasive yet highly effective strategy to accelerate bone healing.
Keyphrases
- bone regeneration
- nitric oxide
- stem cells
- induced apoptosis
- endothelial cells
- mesenchymal stem cells
- cell cycle arrest
- signaling pathway
- nitric oxide synthase
- high throughput
- minimally invasive
- hydrogen peroxide
- wound healing
- transcription factor
- molecularly imprinted
- oxidative stress
- cell death
- bone mineral density
- binding protein
- vascular endothelial growth factor
- endoplasmic reticulum stress
- pi k akt
- epithelial mesenchymal transition
- body composition
- protein kinase
- umbilical cord
- cell proliferation
- single cell
- robot assisted
- bone loss
- electron transfer