Effect of thrombin on permeability of human epithelial cell monolayers

被引:19
|
作者
Hayashi, S [1 ]
Takeuchi, K [1 ]
Suzuki, S [1 ]
Tsunoda, T [1 ]
Tanaka, C [1 ]
Majima, Y [1 ]
机构
[1] Mie Univ, Sch Med, Dept Otorhinolaryngol, Tsu, Mie 5148507, Japan
关键词
thrombin; receptor; PAR-1; airway barrier; asthma; calu-3; monolayer; mannitol; albumin; electrical resistance; stress fibers;
D O I
10.1159/000089718
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Epithelial cells play an important role in maintaining the airway barrier, which is impaired in inflammatory conditions. Recently, thrombin was reported to be increased in the airway of patients with asthma, and thrombin has been shown to increase the permeability of endothelial cell monolayers. Therefore, we suspected that thrombin affects airway permeability. Calu-3 cell monolayers were established on microporous membranes of tissue culture cell inserts. We examined the effects of topically applied thrombin or thrombin receptor-activating peptide (TRAP) on: (1) transepithelial permeability (luminal to serosal transfer) of radiolabeled mannitol and albumin, (2) changes in electrical resistance, and (3) actin fiber content as assessed by fluorescence microscopy. Compared with untreated control cultures, treatment of the monolayers for 24 h with thrombin or TRAP significantly decreased the electrical resistance and increased the permeability to mannitol and albumin. In addition, these treatments enhanced the appearance of actin stress fibers, and small gaps became visible at areas of cell-cell contact. Thrombin appears to increase epithelial permeability by receptor-mediated reorganization of the actin network in airway epithelial cells. This is likely to contribute to the impairment of the airway barrier function. Copyright (C) 2006 S. Karger AG, Basel.
引用
收藏
页码:46 / 52
页数:7
相关论文
共 50 条
  • [11] PROTAMINE INCREASES THE PERMEABILITY OF CULTURED EPITHELIAL MONOLAYERS
    PETERSON, MW
    GRUENHAUPT, D
    JOURNAL OF APPLIED PHYSIOLOGY, 1990, 68 (01) : 220 - 227
  • [12] Permeability properties of monolayers of the human trophoblast cell line BeWo
    Liu, F
    Soares, MJ
    Audus, KL
    AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 273 (05): : C1596 - C1604
  • [13] EFFECT OF ETHANOL ON PARACELLULAR PERMEABILITY OF CACO-2 INTESTINAL EPITHELIAL MONOLAYERS
    MA, TY
    HOA, N
    NGUYEN, D
    GASTROENTEROLOGY, 1995, 108 (04) : A155 - A155
  • [14] Local Influence of Cell Viability on Stretch-Induced Permeability of Alveolar Epithelial Cell Monolayers
    Song, M. J.
    Davis, C. I.
    Lawrence, G. G.
    Margulies, S. S.
    CELLULAR AND MOLECULAR BIOENGINEERING, 2016, 9 (01) : 65 - 72
  • [15] Local Influence of Cell Viability on Stretch-Induced Permeability of Alveolar Epithelial Cell Monolayers
    M. J. Song
    C. I. Davis
    G. G. Lawrence
    S. S. Margulies
    Cellular and Molecular Bioengineering, 2016, 9 : 65 - 72
  • [16] EFFECTS OF HUMAN NEUTROPHIL CHEMOTAXIS ACROSS HUMAN-ENDOTHELIAL CELL MONOLAYERS ON THE PERMEABILITY OF THESE MONOLAYERS TO IONS AND MACROMOLECULES
    HUANG, AJ
    FURIE, MB
    NICHOLSON, SC
    FISCHBARG, J
    LIEBOVITCH, LS
    SILVERSTEIN, SC
    JOURNAL OF CELLULAR PHYSIOLOGY, 1988, 135 (03) : 355 - 366
  • [17] Selective increase of the permeability of polarized epithelial cell monolayers by Helicobacter pylori vacuolating toxin
    Papini, E
    Satin, B
    Norais, N
    de Bernard, M
    Telford, JL
    Rappuoli, R
    Montecucco, C
    JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (04): : 813 - 820
  • [18] EFFECT OF CHITOSAN ON THE PERMEABILITY OF MONOLAYERS OF INTESTINAL EPITHELIAL-CELLS (CACO-2)
    ARTURSSON, P
    LINDMARK, T
    DAVIS, SS
    ILLUM, L
    PHARMACEUTICAL RESEARCH, 1994, 11 (09) : 1358 - 1361
  • [19] Increased permeability of intestinal epithelial monolayers mediated by electroporation
    Ghartey-Tagoe, EB
    Morgan, JS
    Neish, AS
    Prausnitz, MR
    JOURNAL OF CONTROLLED RELEASE, 2005, 103 (01) : 177 - 190
  • [20] CALCIUM IONOPHORE INCREASES THE PERMEABILITY OF CULTURED EPITHELIAL MONOLAYERS
    PETERSON, MW
    GRUENHAUPT, D
    CLINICAL RESEARCH, 1989, 37 (04): : A920 - A920