Basic research in enhancement of permeability in endothelial cells for the development of a bioartificial glomerulus

  • Minh Vu Duc
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Yokoyama Tun Aung
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Sawada Kaichiro
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Fujimura Satoshi
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Sawaya Asako
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Tatsumi Ryoko
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Miyakogawa Takayo
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Hirukawa Takashi
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Kanai Genta
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Miyamoto Yoshiyasu
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Tanaka Reika
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Suzuki Hajime
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Kakuta Takatoshi
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine
  • Saito Akira
    Division of Nephrology, Endocrinology and Metabolism, Department of Medicine, Tokai University School of Medicine

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Other Title
  • バイオ人工糸球体開発における内皮細胞の透過性亢進技術の検討
  • バイオ ジンコウ シキュウタイ カイハツ ニ オケル ナイヒ サイボウ ノ トウカセイ コウシン ギジュツ ノ ケントウ

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Abstract

For the development of a bioartificial glomerulus, in which the inner surface of hollow fibers is lined by endothelial cells, it is essential to increase the permeability of the cells in order to achieve a sufficient ultrafiltrate. We tried to increase it using an actin-microfilament polymerization inhibitor, cytochalasin B (CyB), to enlarge fenestrae diameter of the endothelial cells. CyB was added for 2h at a final concentrations of 20, 30, 40 and 50μg/mL to culture medium of confluent rat glomerular endothelial cells (RGEC) and human umbilical vein endothelial cells (HUVEC). After CyB treatment cell viability was evaluated with Cell Counting Kit-8, and fenestrae diameter of the cells was measured by scanning electron microscopy (SEM), and ultrafiltrate rate through the cell-attached semipermeable membrane was detected under 130mmHg of hydrostatic pressure at days 1, 4, 7. After exposure of platelet-rich plasma, platelet adhesions on CyB-treated and nontreated cells were determined by SEM. Fifty μg/mL of CyB was the best concentration in terms of the cell viability and enhanced ultrafiltrate rate. Scanning electron microscopy demonstrated a larger average diameter of fenestrae on CyB-treated endothelial cells at 50μg/mL of CyB, compared with non-treated cells and CyB-treated cells at 20, 30, and 40μg/mL of CyB. This phenomenon also lasted for at least 7 days. Under 130mmHg hydrostatic pressure, the CyB-treated cells at 50μg/mL of CyB produced significantly more ultrafiltration than the non-treated control group and CyB-treated group at other CyB concentrations, and this increase was maintained for at least 7 days. Horseradish peroxidase (HRP) permeability acutely and reversibly increased in the CyB-treated group compared with that in the non-treated control group. The platelet adherence test showed that CyB did not deteriorate the antithrombogenic property of endothelial cells. These findings indicate that CyB is potentially applicable for the enhancement of endothelial cell permeability in a bioartificial glomerulus.

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