Mesenchymal stem cells transmigrate across brain microvascular endothelial cell monolayers through transiently formed inter-endothelial gaps

• Published in: Neuroscience letters 2011-09, Vol.502 (1), p.41-45
• Main Authors: Matsushita, Takashi, Kibayashi, Tatsuya, Katayama, Takahiro, Yamashita, Yuuki, Suzuki, Syuuichirou, Kawamata, Jun, Honmou, Osamu, Minami, Masabumi, Shimohama, Shun
• Format: Article
• Language: English
• Subjects: Animals; Animals, Genetically Modified; Biological and medical sciences; Blood-Brain Barrier - physiology; Blood–brain barrier; Brain microvascular endothelial cells; Cells, Cultured; Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges; Coculture Techniques; Female; Fundamental and applied biological sciences. Psychology; Gap Junctions - physiology; Male; Mesenchymal stem cells; Mesenchymal Stromal Cells - physiology; Molecular Imaging - methods; Rats; Rats, Sprague-Dawley; Time-Lapse Imaging - methods; Transendothelial and Transepithelial Migration - physiology; Transmigration; Vertebrates: nervous system and sense organs
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2011.07.021

► We developed an in vitro model to study mesenchymal stem cell (MSC) transmigration. ► MSCs were localized predominantly in the subendothelial space after transmigration. ► MSCs transmigrated without impairing BBB barrier integrity. ► Time-lapse imaging showed MSC transendothelial migration via a paracellular pathway. Mesenchymal stem cells (MSCs) hold much promise for cell therapy for neurological diseases such as cerebral ischemia and Parkinson's disease. Intravenously administered MSCs accumulate in lesions within the brain parenchyma, but little is known of the details of MSC transmigration across the blood–brain barrier (BBB). To study MSC transmigration across the BBB, we developed an in vitro culture system consisting of rat brain microvascular endothelial cells (BMECs) and bone marrow-derived MSCs using Transwell or Millicell culture inserts. Using this system, we first investigated the influence of the number of MSCs added to the upper chamber on BMEC barrier integrity. The addition of MSCs at a density of 1.5 × 10 5 cells/cm 2 led to disruption of the BMEC monolayer structure and decreased barrier function as measured by the transendothelial electrical resistance (TEER). When applied at a density of 1.5 × 10 4 cells/cm 2, neither remarkable disruption of the BMEC monolayers nor a significant decrease in TEER was observed until at least 12 h. After cultivation for 24 h under this condition, MSCs were found in the subendothelial space or beneath the insert membrane, suggesting that MSCs transmigrate across BMEC monolayers. Time-lapse imaging revealed that MSCs transmigrated across the BMEC monolayers through transiently formed intercellular gaps between the BMECs. These results show that our in vitro culture system consisting of BMECs and MSCs is useful for investigating the molecular and cellular mechanisms underlying MSC transmigration across the BBB.