The effect of depolarization and calcium ion influx on synaptosomal microtubules

1983 ◽  
Vol 11 (1) ◽  
pp. 86-87 ◽  
Author(s):  
RICHARD CUMMING ◽  
ROBERT D. BURGOYNE ◽  
E. GEORGE GRAY
Keyword(s):  
1994 ◽  
Vol 62 (6) ◽  
pp. 1255-1261 ◽  
Author(s):  
Peter Bielfeld ◽  
Robert A. Anderson ◽  
Steven R. Mack ◽  
Christopher J. De Jonge ◽  
Lourens J.D. Zaneveld

1978 ◽  
Vol 172 (3) ◽  
pp. 549-556 ◽  
Author(s):  
J P Singh ◽  
D F Babcock ◽  
H A Lardy

Capacitation (modifications required for gamete fusion) is produced by incubating guinea-pig spermatozoa in vitro in a chemically defined medium. It is shown that during such incubation a net uptake of Ca2+ by the sperm occurs in two distinguishable phases. An initial loose association of Ca2+, possibly to surface sites, is unaffected by agents (Mg2+, inhibitors of mitochondiral function) that prevent or delay the exocytotic spermatozoal acrosome reaction. The time course of a secondary Ca2+ uptake parallels or slightly precedes the time course of the acrosome reaction. This parallelism is maintained during a variety of treatments that either expedite (local anaesthetics, ionophore A23187, Triton X-100) or delay (Mg2+, low external Ca2+) the acrosome reaction. We conclude that the secondary Ca2+ influx described herein apparently serves to link alterations of the spermatozoal membrane to subsequent contractile and secretory components of the capacitation sequence.


2021 ◽  
Author(s):  
Yunshan Guo ◽  
Dingjun Hao

Abstract Background: The molecular mechanisms by which dexamethasone (Dex) induces apoptosis in osteoblasts remain unclear.Materials and Methods: MC3T3-E1 cells were treated with 0, 10-8, 10-6, and 10-4 M Dex for 24 h. The expression of ATF6, and phosphorylated PERK and IRE1, cell apoptosis, and the activity of caspase-12 and caspase-3 were measured. The expression of CHOP and the rate of influx of calcium ions were also measured in cells treated with 0 and 10-4 M Dex for 24 h. The effect of 2-APB treatment was assessed in cells treated with 0 or 10-4 M Dex.Results: The levels of ATF6 and phosphorylated PERK and IRE1 increased in a dose-dependent manner in MC3T3-E1 cells treated with 10-8, 10-6, and 10-4 M Dex, compared to in cells treated with 0 M Dex (P <0.05). Cells treated with 10-6 and 10-4 M Dex had significantly increased cell apoptosis rates and caspase-12 and caspase-3 activity compared to the control (P <0.05). Cells treated with 10-4 M Dex had significantly increased levels of CHOP and calcium ion influx rates compared to in the control (P <0.05). Combined treatment with 10-4 M Dex and 2-APB abrogated the observed increases in cell apoptosis and the activity of caspase-12 and caspase-3 (P>0.05). Conclusion: High doses of Dex induce endoplasmic reticulum stress-mediated apoptosis by promoting calcium ion influx-dependent expression of CHOP, and the activation of caspase-12 and caspase-3 in osteoblasts. Combined treatment with 2-APB protects the cells from the effects of Dex, preventing endoplasmic reticulum stress-mediated apoptosis.


2020 ◽  
Vol 50 (7) ◽  
pp. 914-919
Author(s):  
E. F. Khaziev ◽  
D. V. Balashova ◽  
A. N. Tsentsevitsky ◽  
E. A. Bukharaeva ◽  
D. V. Samigullin

1980 ◽  
Vol 29 (4) ◽  
pp. 479-481 ◽  
Author(s):  
J.M. Van Nueten ◽  
P.M. Vanhoutte

1987 ◽  
Vol 12 (4) ◽  
pp. 345-355 ◽  
Author(s):  
Hiroshi Komada ◽  
Hiroshi Nakabayashi ◽  
Hiroshi Nakano ◽  
Hideki Takanari ◽  
Takao Takahashi ◽  
...  

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