Long-term mechanical loading is required for the formation of 3D bioprinted functional osteocyte bone organoids.
Jianhua ZhangJulia GriesbachMarsel GaneyevAnna-Katharina ZehnderPeng ZengGian Nutal SchädliAnke de LeeuwYu-Xiao LaiMarina RubertRalph MüllerPublished in: Biofabrication (2022)
Mechanical loading has been shown to influence various osteogenic responses of bone-derived cells and bone formation in vivo . However, the influence of mechanical stimulation on the formation of bone organoid in vitro is not clearly understood. Here, three-dimensional (3D) bioprinted human mesenchymal stem cells-laden graphene oxide composite scaffolds were cultured in a novel cyclic-loading bioreactors for up to 56 d. Our results showed that mechanical loading from day 1 (ML01) significantly increased organoid mineral density, organoid stiffness, and osteoblast differentiation compared with non-loading and mechanical loading from day 21. Importantly, ML01 stimulated collagen I maturation, osteocyte differentiation, lacunar-canalicular network formation and YAP expression on day 56. These finding are the first to reveal that long-term mechanical loading is required for the formation of 3D bioprinted functional osteocyte bone organoids. Such 3D bone organoids may serve as a human-specific alternative to animal testing for the study of bone pathophysiology and drug screening.
Keyphrases
- bone mineral density
- mesenchymal stem cells
- endothelial cells
- bone regeneration
- soft tissue
- bone loss
- induced pluripotent stem cells
- bone marrow
- emergency department
- postmenopausal women
- poor prognosis
- induced apoptosis
- gene expression
- wastewater treatment
- signaling pathway
- genome wide
- single cell
- dna methylation
- cell therapy
- cell death
- binding protein
- drug induced
- pi k akt