# Non-physiological potassium concentrations in commercial culture media trigger acute seizure-like activity in human iPSC-derived neurons

**Authors:** Tim Lyckenvik, Julia Izsak, Erik Arthursson, My Forsberg, Kalle Johansson, Henrik Zetterberg, Markus Axelsson, Pontus Wasling, Eric Hanse, Stephan Theiss, Sebastian Illes

PMC · DOI: 10.1038/s41598-026-43094-7 · 2026-03-18

## TL;DR

Common cell culture media cause abnormal seizure-like activity in human neurons due to incorrect potassium levels.

## Contribution

The study reveals that standard culture media have non-physiological potassium levels, leading to abnormal neuronal activity.

## Key findings

- Commercial culture media have higher potassium than human CSF, causing seizure-like activity in neurons.
- Neurons in human CSF show different activity than those in standard culture media.
- This suggests in vitro experiments may not accurately reflect physiological brain activity.

## Abstract

Neuronal in vitro cultures are pivotal for studying brain electrophysiological function and dysfunction. Neuronal activity and communication are regulated by extracellular ion concentrations. Therefore, cell culture medium ion concentrations should ideally mimic those of cerebrospinal fluid (CSF)—considered as the milieu for brain cells in vivo. In this study, we demonstrate that commonly used cell culture media, including NeurobasalTM (+ /− A), Neurobasal PlusTM, and BrainPhysTM media, do not accurately replicate human CSF ion concentrations. Using human iPSC-derived neuronal networks on microelectrode arrays, we compare neuronal activity in standard culture media with that in physiological artificial cerebrospinal fluid (aCSF) and in human cerebrospinal fluid. We show that supraphysiological potassium levels in culture media acutely induce seizure-like neuronal network activity compared with both physiological aCSF and human CSF. Importantly, human neurons exposed to human CSF obtained from healthy individuals show fundamentally different neuronal network activity than neurons exposed to currently used cell culture media. These findings raise a critical question: How can human in vitro neuronal activity be defined as physiological and reliably distinguished from pathophysiological activity, if the routinely used ion concentrations in in vitro experiments are causing aberrant neuronal activity that is fundamentally different from that of human neurons exposed to human CSF?

The online version contains supplementary material available at 10.1038/s41598-026-43094-7.

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** GDNF (glial cell derived neurotrophic factor) [NCBI Gene 2668] {aka ATF, ATF1, ATF2, HFB1-GDNF, HSCR3}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, MRAP (melanocortin 2 receptor accessory protein) [NCBI Gene 56246] {aka B27, C21orf61, FALP, GCCD2, MRAP1}
- **Diseases:** seizure (MESH:D012640), spike (MESH:D031261), aCSF (MESH:D002559)
- **Chemicals:** K+ (MESH:D011188), N2 (MESH:D009584), D-glucose (MESH:D005947), NaCl (MESH:D012965), lipids (MESH:D008055), bicarbonate (MESH:D001639), GlutaMAX (MESH:C054122), 4-AP (MESH:D015761), F12 (MESH:C007782), Cl- (MESH:D002713), ascorbic acid (MESH:D001205), Ti (MESH:D014025), CO2 (MESH:D002245), penicillin (MESH:D010406), chloride (MESH:D002712), PLO (MESH:C008973), glutamine (MESH:D005973), vitamin A (MESH:D014801), amino acids (MESH:D000596), KCl (MESH:D011189), calcium (MESH:D002118), streptomycin (MESH:D013307), Magnesium (MESH:D008274), Na+ (MESH:D012964), NaHCO (-), 2-mercaptoethanol (MESH:D008623)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Rodentia (rodent, order) [taxon 9989]
- **Cell lines:** hCSF — Homo sapiens (Human), Transformed cell line (CVCL_XY86)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13000296/full.md

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Source: https://tomesphere.com/paper/PMC13000296