4.8 Article

Stretchable Mesh Nanoelectronics for 3D Single-Cell Chronic Electrophysiology from Developing Brain Organoids

Journal

ADVANCED MATERIALS
Volume 34, Issue 11, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202106829

Keywords

bioelectronics; brain organoids; electrophysiology; nanoelectronics; neural interface; stretchable electronics

Funding

  1. NIH/NIMH [1RF1MH123948]
  2. NSF through the Harvard University Materials Research Science and Engineering Center Grant [DMR-2011754]
  3. Harvard University Center for Nanoscale Systems - NSF
  4. Aramont Fund for Emerging Science Research
  5. William F. Milton Fund

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This study reports a cyborg brain organoid platform that utilizes stretchable electrode arrays to establish long-term stable electrical contacts with brain organoids, enabling continuous recording and analysis of the electrical properties during the development of brain organoids.
Human induced pluripotent stem cell derived brain organoids have shown great potential for studies of human brain development and neurological disorders. However, quantifying the evolution of the electrical properties of brain organoids during development is currently limited by the measurement techniques, which cannot provide long-term stable 3D bioelectrical interfaces with developing brain organoids. Here, a cyborg brain organoid platform is reported, in which tissue-like stretchable mesh nanoelectronics are designed to match the mechanical properties of brain organoids and to be folded by the organogenetic process of progenitor or stem cells, distributing stretchable electrode arrays across the 3D organoids. The tissue-wide integrated stretchable electrode arrays show no interruption to brain organoid development, adapt to the volume and morphological changes during brain organoid organogenesis, and provide long-term stable electrical contacts with neurons within brain organoids during development. The seamless and noninvasive coupling of electrodes to neurons enables long-term stable, continuous recording and captures the emergence of single-cell action potentials from early-stage brain organoid development.

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