scholarly journals Rapid Morphological Changes of Bovine Brain Microvascular Endothelial Cells on Extracellular Matrices

1992 ◽  
Vol 32 (8) ◽  
pp. 549-553
Author(s):  
Takaaki KANEKO ◽  
Izumi NAGATA ◽  
Susumu MIYAMOTO ◽  
Hiroaki KUBO ◽  
Haruhiko KIKUCHI ◽  
...  
Keyword(s):  
Endothelial Cells ◽  
Morphological Changes ◽  
Bovine Brain ◽  
Extracellular Matrices ◽  
Microvascular Endothelial Cells ◽  
Brain Microvascular Endothelial Cells ◽  
Microvascular Endothelial

Hypoxia-induced alterations in Ca2+mobilization in brain microvascular endothelial cells

2000 ◽  
Vol 279 (5) ◽  
pp. H2310-H2318 ◽  
Author(s):  
Chiwaka Kimura ◽  
Masahiro Oike ◽  
Yushi Ito
Keyword(s):  
Endothelial Cells ◽  
Bovine Brain ◽  
Microvascular Endothelial Cells ◽  
Dependent Manner ◽  
Brain Microvascular Endothelial Cells ◽  
Cellular Mechanisms ◽  
Concentration Dependent Manner ◽  
Intracellular Ca ◽  
Microvascular Endothelial ◽  
Hypoxia Reoxygenation

To investigate the possible cellular mechanisms of the ischemia-induced impairments of cerebral microcirculation, we investigated the effects of hypoxia/reoxygenation on the intracellular Ca2+ concentration ([Ca2+]i) in bovine brain microvascular endothelial cells (BBEC). In the cells kept in normal air, ATP elicited Ca2+ oscillations in a concentration-dependent manner. When the cells were exposed to hypoxia for 6 h and subsequent reoxygenation for 45 min, the basal level of [Ca2+]i was increased from 32.4 to 63.3 nM, and ATP did not induce Ca2+ oscillations. Hypoxia/reoxygenation also inhibited capacitative Ca2+entry (CCE), which was evoked by thapsigargin (Δ[Ca2+]i-CCE: control, 62.3 ± 3.1 nM; hypoxia/reoxygenation, 17.0 ± 1.8 nM). The impairments of Ca2+ oscillations and CCE, but not basal [Ca2+]i, were restored by superoxide dismutase and the inhibitors of mitochondrial electron transport, rotenone and thenoyltrifluoroacetone (TTFA). By using a superoxide anion (O2 −)-sensitive luciferin derivative MCLA, we confirmed that the production of O2 − was induced by hypoxia/reoxygenation and was prevented by rotenone and TTFA. These results indicate that hypoxia/reoxygenation generates O2 − at mitochondria and impairs some Ca2+mobilizing properties in BBEC.

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