Abstract

The blood-brain barrier (BBB) is formed by brain capillary endothelial cells (BECs) supported by pericytes and astrocytes. The BBB maintains homeostasis and protects the brain against toxic substances circulating in the blood, meaning that only a few drugs can pass the BBB. Thus, for drug screening, understanding cell interactions, and pathology, in vitro BBB models have been developed using BECs from various animal sources. When comparing models of different species, differences exist especially in regards to the transendothelial electrical resistance (TEER). Thus, we compared primary mice, rat, and porcine BECs (mBECs, rBECs, and pBECs) cultured in mono- and co-culture with astrocytes, to identify species-dependent differences that could explain the variations in TEER and aid to the selection of models for future BBB studies. The BBB models based on primary mBECs, rBECs, and pBECs were evaluated and compared in regards to major BBB characteristics. The barrier integrity was evaluated by the expression of tight junction proteins and measurements of TEER and apparent permeability (Papp). Additionally, the cell size, the functionality of the P-glycoprotein (P-gp) efflux transporter, and the expression of the transferrin receptor were evaluated and compared. Expression and organization of tight junction proteins were in all three species influenced by co-culturing, supporting the findings, that TEER increases after co-culturing with astrocytes. All models had functional polarised P-gp efflux transporters and expressed the transferrin receptor. The most interesting discovery was that even though the pBECs had higher TEER than rBECs and mBECs, the Papp did not show the same variation between species, which could be explained by a significantly larger cell size of pBECs. In conclusion, our results imply that the choice of species for a given BBB study should be defined from its purpose, instead of aiming to reach the highest TEER, as the models studied here revealed similar BBB properties.

Highlights

  • The blood-brain barrier (BBB) is a protective barrier formed by non-fenestrated brain capillary endothelial cells (BECs), which are supported by pericytes embedded in the basement membrane and astrocytic endfeet [1]

  • The Mouse brain capillary endothelial cells (mBECs) exhibited slower cell growth than the Rat brain capillary endothelial cells (rBECs) and Porcine brain capillary endothelial cells (pBECs) and were cultured for an extra day before being re-seeded in the hanging culture inserts (Fig 1A). mBECs were isolated on day -4, while rBECs and pBECs were isolated on day -3

  • The isolated microvessels are recognized as small pearls on a string, and after one day in culture the BECs start to proliferate from the microvessels and grow into a monolayer reaching a confluence level of 80–90% on day 0 (Fig 1B)

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Summary

Introduction

The blood-brain barrier (BBB) is a protective barrier formed by non-fenestrated brain capillary endothelial cells (BECs), which are supported by pericytes embedded in the basement membrane and astrocytic endfeet [1]. Pericytes cover approximately 30% of brain capillaries, while. In vitro blood-brain barrier models (MST, NH, AB, LBT), Kong Christian d. Leo Nielsen og Hustru Karen Margrethe Nielsens Legat for Lægevidenskabelig Grundforskning (https://www.njordlaw.com/da/om-njord/fonde-oglegater/fhv-dir-leo-nielsen-og-hustru-karenmargrethe-nielsens-legat-for-laegevidenskabeliggrundforskning/) (MST), Augustinus fonden (https://augustinusfonden.dk/) (AB, LBT), Danielsens fond (https://danielsensfond.dk/)(AB, LBT), the Lundbeck Foundation Research Initiative on Brain Barriers and Drug Delivery The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

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