Format

Send to

Choose Destination
J Biomed Mater Res A. 2018 Mar;106(3):629-640. doi: 10.1002/jbm.a.36267. Epub 2017 Oct 23.

Hydrostatic pressure in combination with topographical cues affects the fate of bone marrow-derived human mesenchymal stem cells for bone tissue regeneration.

Author information

1
Institute of Science and Technology in Medicine, Keele University, Medical School, Guy Hilton Research Centre, UHNM, Stoke-on-Trent, United Kingdom.
2
Department of Engineering, School of Science and Technology, Nottingham Trent University, Nottingham, United Kingdom.

Abstract

Topographical and mechanical cues are vital for cell fate, tissue development in vivo, and to mimic the native cell growth environment in vitro. To date, the combinatory effect of mechanical and topographical cues as not been thoroughly investigated. This study investigates the effect of PCL nanofiber alignment and hydrostatic pressure on stem cell differentiation for bone tissue regeneration. Bone marrow-derived human mesenchymal stem cells were seeded onto standard tissue culture plastic and electrospun random and aligned nanofibers. These substrates were either cultured statically or subjected to intermittent hydrostatic pressure at 270 kPa, 1 Hz for 60 min daily over 21 days in osteogenic medium. Data revealed higher cell metabolic activities for all mechanically stimulated cell culture formats compared with non-stimulated controls; and random fibers compared with aligned fibers. Fiber orientation influenced cell morphology and patterns of calcium deposition. Significant up-regulation of Collagen-I, ALP, and Runx-2 were observed for random and aligned fibers following mechanical stimulation; highest levels of osteogenic markers were expressed when hydrostatic pressure was applied to random fibers. These results indicate that fiber alignment and hydrostatic pressure direct stem cell fate and are important stimulus for tissue regeneration.

KEYWORDS:

bone regeneration; hydrostatic pressure; mechanical stimulation; nano-topography; stem cells

Supplemental Content

Full text links

Icon for Wiley Icon for PubMed Central
Loading ...
Support Center