Extracellularly Detectable Electrochemical Signals of Living Cells Originate from Metabolic Reactions.
Kyeong-Mo KooChang-Dae KimHuijung KimYeon-Woo ChoIntan Rosalina SuhitoTae-Hyung KimPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2023)
Direct detection of cellular redox signals has shown immense potential as a novel living cell analysis tool. However, the origin of such signals remains unknown, which hinders the widespread use of electrochemical methods for cellular research. In this study, the authors found that intracellular metabolic pathways that generate adenosine triphosphate (ATP) are the main contributors to extracellularly detectable electrochemical signals. This is achieved through the detection of living cells (4,706 cells/chip, linearity: 0.985) at a linear range of 7,466-48,866. Based on this discovery, the authors demonstrated that the cellular signals detected by differential pulse voltammetry (DPV) can be rapidly amplified with a developed medium containing metabolic activator cocktails (MACs). The DPV approach combined with MAC treatment shows a remarkable performance to detect the effects of the anticancer drug CPI-613 on cervical cancer both at a low drug concentration (2 µm) and an extremely short treatment time (1 hour). Furthermore, the senescence of mesenchymal stem cells could also be sensitively quantified using the DPV+MAC method even at a low passage number (P6). Collectively, their findings unveiled the origin of redox signals in living cells, which has important implications for the characterization of various cellular functions and behaviors using electrochemical approaches.
Keyphrases
- living cells
- fluorescent probe
- label free
- single molecule
- gold nanoparticles
- mesenchymal stem cells
- ionic liquid
- molecularly imprinted
- high throughput
- cell therapy
- stem cells
- small molecule
- emergency department
- electron transfer
- mass spectrometry
- high resolution
- circulating tumor cells
- single cell
- risk assessment
- real time pcr
- immune response
- cell proliferation
- climate change
- nuclear factor
- toll like receptor
- inflammatory response
- endoplasmic reticulum stress
- smoking cessation