Triggering the activation of Activin A type II receptor in human adipose stem cells towards tenogenic commitment using mechanomagnetic stimulation

last updated: 2018-10-17
ProjectNORTE45_3Bs - RL2 :: publications list
TitleTriggering the activation of Activin A type II receptor in human adipose stem cells towards tenogenic commitment using mechanomagnetic stimulation
Publication TypePapers in Scientific Journals
Year of Publication2018
AuthorsGonçalves A. I., Rotherham M., Markides H., Rodrigues M. T., Reis R. L., Gomes M. E., and Haj A. E.
Abstract

Stem cell therapies hold potential to stimulate tendon regeneration and homeostasis, which is maintained in response to the native mechanical environment. Activins are members of the mechano-responsive TGF-β superfamily that participates in the regulation of several downstream biological processes. Mechanosensitive membrane receptors such as activin can be activated in different types of stem cells via magnetic nanoparticles (MNPs) through remote magnetic actuation resulting in cell differentiation. In this work, we target the Activin receptor type IIA (ActRIIA) in human adipose stem cells (hASCs), using anti-ActRIIA functionalized MNPs, externally activated through a oscillating magnetic bioreactor. Upon activation, the phosphorylation of Smad2/3 is induced allowing translocation of the complex to the nucleus, regulating tenogenic transcriptional responses. Our study demonstrates the potential remote activation of MNPs tagged hASCs to trigger the Activin receptor leading to tenogenic differentiation. These results may provide insights toward tendon regeneration therapies.

JournalNanomedicine: Nanotechnology, Biology and Medicine
Volume14
Issue4
Pagination1149-1159
Date Published2018-02-19
PublisherElsevier
ISSN1549-9634
DOI10.1016/j.nano.2018.02.008
URLhttp://www.nanomedjournal.com/article/S1549-9634(18)30041-8/fulltext
KeywordsActivin A receptor, Human adipose derived stem cells, Magnetic nanoparticles, Tendon Tissue Engineering, TGF-β/Smad2/3 signaling pathway
RightsopenAccess
Peer reviewedyes
Statuspublished

Back to top