Change of potassium current density in rabbit corneal epithelial cells during maturation and cellular senescence

被引:3
作者
Chang, SW
Chang, GJ
Su, MJ
机构
[1] Natl Taiwan Univ, Coll Med, Dept Pharmacol, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, Far Eastern Mem Hosp, Dept Ophthalmol, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Ophthalmol, Taipei, Taiwan
[4] Taipei Med Univ, Dept Ophthalmol, Taipei, Taiwan
[5] Chang Gung Univ, Grad Inst Clin Med Sci, Tao Yuan, Taiwan
关键词
cellular senescence; corneal epithelium; maturation; potassium current;
D O I
10.1016/S0929-6646(09)60103-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Voltage-gated potassium (K+) channels may participate in cellular developmental regulation, including cell differentiation, proliferation and apoptosis. This study investigated the change of K+ current densities in corneal epithelial cells during maturation and cellular senescence. Methods: New Zealand white rabbits were divided into three age groups: newborn (<= 7 days old, n = 18); young (8-12 weeks old, n = 59); and adult (20-28 weeks old, n = 16). Rabbit Corneal epithelial cells were subdivided into the following three groups: small cells with capacitance < 6.0 pF; medium cells with capacitance 6.0-10.0 pF; and large cells with capacitance > 10.0 pF. Using a whole-cell clamp technique, K+ current was recorded and current densities were calculated. Differences in K+ current densities among newborn, young and adult rabbits, as well as differences among small, medium and large cells, were analyzed. Results: We delineated two types of cells manifesting different amplitudes of depolarization-activated K+ outward currents. The averaged current density of type 1 response cells was significantly larger than that of type 2 cells in newborn, young, and adult groups. For newborn epithelial cells, the depolarization-gated outward K+ current density decreased from small to medium to large cells (p = 0.049, at a membrane potential of 140 mV). A similar pattern of change in current density was also delineated for these cell sizes in young and adult rabbit corneal cells (p < 0.001 for both young and adult rabbits). An increase in depolarizationgated outward K+ current density was also delineated from newborn to young to adult rabbits (p < 0.00 1, p < 0.001 and p < 0.006 for small, medium and large cells, respectively, at a membrane potential of 140 mV). Conclusions: Corneal epithelial cells expressed K+ channel densities that were distinct from basal to superficial cells and from newborn to adult rabbits.
引用
收藏
页码:7 / 16
页数:10
相关论文
共 49 条
  • [1] INTRACELLULAR IONIC VARIATIONS IN THE APOPTOTIC DEATH OF L-CELLS BY INHIBITORS OF CELL-CYCLE PROGRESSION
    BARBIERO, G
    DURANTI, F
    BONELLI, G
    AMENTA, JS
    BACCINO, FM
    [J]. EXPERIMENTAL CELL RESEARCH, 1995, 217 (02) : 410 - 418
  • [2] Beebe DC, 1996, INVEST OPHTH VIS SCI, V37, P1815
  • [3] Developmental changes in the functional characteristics and expression of voltage-gated K+ channel currents in rat aortic myocytes
    Belevych, AE
    Beck, R
    Tammaro, P
    Poston, L
    Smirnov, SV
    [J]. CARDIOVASCULAR RESEARCH, 2002, 54 (01) : 152 - 161
  • [4] Caspase independent/dependent regulation of K+, cell shrinkage, and mitochondrial membrane potential during lymphocyte apoptosis
    Bortner, CD
    Cidlowski, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (31) : 21953 - 21962
  • [5] A primary role for K+ and Na+ efflux in the activation of apoptosis
    Bortner, CD
    Hughes, FM
    Cidlowski, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) : 32436 - 32442
  • [6] BUCK RC, 1985, INVEST OPHTH VIS SCI, V26, P1296
  • [7] Campisi J, 2000, IN VIVO, V14, P183
  • [8] Benzalkonium chloride and gentamicin cause a leak in corneal epithelial cell membrane
    Chang, SW
    Chi, RF
    Wu, CC
    Su, MJ
    [J]. EXPERIMENTAL EYE RESEARCH, 2000, 71 (01) : 3 - 10
  • [9] INDUCTION OF MITOSIS IN MATURE NEURONS IN CENTRAL NERVOUS-SYSTEM BY SUSTAINED DEPOLARIZATION
    CONE, CD
    CONE, CM
    [J]. SCIENCE, 1976, 192 (4235) : 155 - 158
  • [10] Dallaporta B, 1998, J IMMUNOL, V160, P5605