Influence of basal media composition on barrier fidelity within human pluripotent stem cell-derived blood-brain barrier models

J Neurochem. 2021 Dec;159(6):980-991. doi: 10.1111/jnc.15532. Epub 2021 Nov 18.

Abstract

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.

Keywords: blood-brain barrier; brain microvascular endothelial cell; human-induced pluripotent stem cell; in vitro model.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Blood-Brain Barrier / cytology
  • Blood-Brain Barrier / drug effects
  • Blood-Brain Barrier / metabolism*
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Cell Membrane Permeability / drug effects
  • Cell Membrane Permeability / physiology*
  • Culture Media / chemistry
  • Culture Media / pharmacology*
  • Culture Media, Serum-Free / chemistry
  • Culture Media, Serum-Free / pharmacology
  • Humans
  • Induced Pluripotent Stem Cells / drug effects
  • Induced Pluripotent Stem Cells / metabolism*

Substances

  • Culture Media
  • Culture Media, Serum-Free