4.7 Article

Wireless Force-Inducing Neuronal Stimulation Mediated by High Magnetic Moment Microdiscs

期刊

ADVANCED HEALTHCARE MATERIALS
卷 11, 期 6, 页码 -

出版社

WILEY
DOI: 10.1002/adhm.202101826

关键词

alternating magnetic fields; lithography; magnetic nanomaterials; magnetic vortices; mechanotransduction; neurostimulation

资金

  1. European Unions Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant [734801]
  2. Spanish AEI grant [PID2019-104604RB]
  3. Basque Country grant [IT1162-19]
  4. University of Texas at San Antonio, Office of the Vice President for Research, Economic Development, and Knowledge Enterprise
  5. National Science Foundation under a CAREER award [CBET - 2044713]
  6. US National Science Foundation [ECCS-1542148]
  7. NSF [DMR 1805585, DMR 1804414]
  8. MARC*U-Star program at the University of Texas at San Antonio [NIH GM007717]

向作者/读者索取更多资源

This study presents a noninvasive technique for manipulating neural activity through magneto-mechanical stimulation using magnetic microdiscs. By inducing mechanical forces on primary neuronal circuits with low-intensity and low-frequency magnetic fields, specific mechanosensitive ion channels can be activated, leading to effective stimulation of hippocampal and cortical neurons.
Noninvasive manipulation of cell signaling is critical in basic neuroscience research and in developing therapies for neurological disorders and psychiatric conditions. Here, the wireless force-induced stimulation of primary neuronal circuits through mechanotransduction mediated by magnetic microdiscs (MMDs) under applied low-intensity and low-frequency alternating magnetic fields (AMFs), is described. MMDs are fabricated by top-down lithography techniques that allow for cost-effective mass production of biocompatible MMDs with high saturation and zero magnetic magnetic moment at remanence. MMDs are utilized as transducers of AMFs into mechanical forces. When MMDs are exposed to primary rat neuronal circuits, their magneto-mechanical actuation triggers the response of specific mechanosensitive ion channels expressed on the cell membranes activating approximate to 50% of hippocampal and approximate to 90% of cortical neurons subjected to the treatment. Mechanotransduction is confirmed by the inhibition of mechanosensitive transmembrane channels with Gd3+. Mechanotransduction mediated by MMDs cause no cytotoxic effect to neuronal cultures. This technology fulfills the requirements of cell-type specificity and weak magnetic fields, two limiting factors in the development of noninvasive neuromodulation therapies and clinical equipment design. Moreover, high efficiency and long-lasting stimulations are successfully achieved. This research represents a fundamental step forward for magneto-mechanical control of neural activity using disc-shaped micromaterials with tailored magnetic properties.

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