Three-dimensional vertical micro-
and nanostructures can enhance
the signal quality of multielectrode arrays and promise to become
the prime methodology for the investigation of large networks of electrogenic
cells. So far, access to the intracellular environment has been obtained
via spontaneous poration, electroporation, or by surface functionalization
of the micro/nanostructures; however, these methods still suffer from
some limitations due to their intrinsic characteristics that limit
their widespread use. Here, we demonstrate the ability to continuously
record both extracellular and intracellular-like action potentials
at each electrode site in spontaneously active mammalian neurons and
HL-1 cardiac-derived cells via the combination of vertical nanoelectrodes
with plasmonic optoporation. We demonstrate long-term and stable recordings
with a very good signal-to-noise ratio. Additionally, plasmonic optoporation
does not perturb the spontaneous electrical activity; it permits continuous
recording even during the poration process and can regulate extracellular
and intracellular contributions by means of partial cellular poration.