A Polymer Bio–Photoelectrolytic Platform for Electrical Signal Measurement and for Light Modulation of Ion Fluxes and Proliferation in a Neuroblastoma Cell Line

Author:

Ciocca Manuela12ORCID,Marcozzi Serena3,Mariani Paolo1,Lacconi Valentina3,Di Carlo Aldo4,Cinà Lucio5,Rosato-Siri Marcelo D.6,Zanon Alessandra6,Cattelan Giada6,Avancini Enrico2,Lugli Paolo2,Priya Shashank7,Camaioni Antonella3,Brown Thomas M.1ORCID

Affiliation:

1. Department of Electronic Engineering University of Rome Tor Vergata Via del Politecnico 1 00133 Rome Italy

2. Faculty of Science and Technology Free University of Bozen-Bolzano Piazza Università 1 39100 Bolzano Italy

3. Department of Biomedicine and Prevention University of Rome Tor Vergata Via Montpellier 1 00133 Rome Italy

4. Istituto di Struttura della Materia CNR-ISM via Fosso del Cavaliere 100 00133 Rome Italy

5. Cicci Research srl. Via Giordania 227 58100 Grosseto Italy

6. Institute for Biomedicine, Eurac Research Affiliated Institute of the University of Lübeck 39100 Bolzano Italy

7. Department of Materials Science and Engineering Pennsylvania State University University Park PA 16802 USA

Abstract

Light control of living systems is an emerging field in bioelectronics, in regenerative medicine and cell‐based therapy. Herein, the design of a semitransparent bio–photoelectrolytic platform for control of a neuroblastoma cell line via light pulses is laid out. The platform is based on conjugated polymer films interfaced with a biological electrolyte solution confined in a compact chamber. Human SH‐SY5Y neuroblastoma cells are cultured for 3 days on the organic semiconductor and subjected to a pulsed light protocol. At the end of the culture time, proliferative activity of cells on the polymer film subjected to light pulses is reduced by 50% compared to the cultures kept in dark. An increase in intracellular Ca2+ level is observed, indicating a significant perturbation of the equilibrium potential of the cells. It is shown that the platform, in a sandwich‐type closed architecture with two transparent electrodes, can provide a tool for the initial recording of bioelectrical photovoltage signals (mV) that can complement analysis with more sophisticated electrophysiological tools. Obtained results can pave the way to new noninvasive photomanipulation techniques to stimulate/control living cells and their proliferation through both optical and electrical stimulation and probes, for application in the fields of biosensing and biomedicine.

Funder

Air Force Office of Scientific Research

Regione Lazio

Università degli Studi di Roma Tor Vergata

Publisher

Wiley

Subject

General Medicine

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