Direct electrical stimulation enhances osteogenesis by inducing Bmp2 and Spp1 expressions from macrophages and preosteoblasts

Kasama Srirussamee, Sahba Mobini, Nigel J. Cassidy, Sarah H. Cartmell

Research output: Contribution to journalArticlepeer-review

Abstract

The capability of electrical stimulation (ES) in promoting bone regeneration has already been addressed in clinical studies. However, its mechanism is still being investigated and discussed. This study aims to investigate the responses of macrophages (J774A.1) and preosteoblasts (MC3T3-E1) to ES and the faradic by-products from ES. It is found that pH of the culture media was not significantly changed, whereas the average hydrogen peroxide concentration was increased by 3.6 and 5.4 µM after 1 and 2 hr of ES, respectively. The upregulation of Bmp2 and Spp1 messenger RNAs was observed after 3 days of stimulation, which is consistent among two cell types. It is also found that Spp1 expression of macrophages was partially enhanced by faradic by-products. Osteogenic differentiation of preosteoblasts was not observed during the early stage of ES as the level of Runx2 expression remains unchanged. However, cell proliferation was impaired by the excessive current density from the electrodes, and also faradic by-products in the case of macrophages. This study shows that macrophages could respond to ES and potentially contribute to the bone formation alongside preosteoblasts. The upregulation of Bmp2 and Spp1 expressions induced by ES could be one of the mechanisms behind the electrically stimulated osteogenesis.

Original languageEnglish
Pages (from-to)3421-3432
Number of pages12
JournalBiotechnology and Bioengineering
Volume116
Issue number12
Early online date20 Aug 2019
DOIs
Publication statusPublished - 1 Dec 2019

Keywords

  • bone regeneration
  • electrical stimulation
  • faradic by-products
  • macrophages
  • preosteoblasts

Fingerprint

Dive into the research topics of 'Direct electrical stimulation enhances osteogenesis by inducing Bmp2 and Spp1 expressions from macrophages and preosteoblasts'. Together they form a unique fingerprint.

Cite this