Influence of basal media composition on barrier fidelity within human pluripotent stem cell-derived blood-brain barrier models.
Emma H NealKetaki A KatdareYajuan ShiNicholas A MarinelliKameron A HagerlaEthan S LippmannPublished in: Journal of neurochemistry (2021)
It is increasingly recognized that brain microvascular endothelial cells (BMECs), the principal component of the blood-brain barrier (BBB), are highly sensitive to soluble cues from both the bloodstream and the brain. This concept extends in vitro, where the extracellular milieu can also influence BBB properties in cultured cells. However, the extent to which baseline culture conditions can affect BBB properties in vitro remains unclear, which has implications for model variability and reproducibility, as well as downstream assessments of molecular transport and disease phenotypes. Here, we explore this concept by examining BBB properties within human-induced pluripotent stem cell (iPSC)-derived BMEC-like cells cultured under serum-free conditions in DMEM/F12 and Neurobasal media, which have fully defined compositions. We demonstrate notable differences in both passive and active BBB properties as a function of basal media composition. Further, RNA sequencing and phosphoproteome analyses revealed alterations to various signaling pathways in response to basal media differences. Overall, our results demonstrate that baseline culture conditions can have a profound influence on the performance of in vitro BBB models, and these effects should be considered when designing experiments that utilize such models for basic research and preclinical assays.
Keyphrases
- blood brain barrier
- endothelial cells
- high glucose
- cerebral ischemia
- stem cells
- induced apoptosis
- induced pluripotent stem cells
- signaling pathway
- white matter
- single cell
- vascular endothelial growth factor
- resting state
- cell therapy
- high throughput
- pluripotent stem cells
- multiple sclerosis
- cell cycle arrest
- cell death
- multidrug resistant
- mass spectrometry
- pi k akt
- klebsiella pneumoniae
- endoplasmic reticulum stress
- molecularly imprinted
- fluorescent probe