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Tytuł pozycji:

The absence of an early calcium response to heavy-ion radiation in Mammalian cells.

Tytuł:
The absence of an early calcium response to heavy-ion radiation in Mammalian cells.
Autorzy:
Du G; Department of Materials Science, Gesellschaft für Schwerionenforschung mbH (GSI), Darmstadt 64291, Germany. />Fischer BE
Voss KO
Becker G
Taucher-Scholz G
Kraft G
Thiel G
Źródło:
Radiation research [Radiat Res] 2008 Sep; Vol. 170 (3), pp. 316-26.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: Bozeman, MT : Radiation Research Society
Original Publication: Charlottesville, VA : Kluge Carden Jennnings Pub. Co.
MeSH Terms:
Heavy Ions*
Calcium/*metabolism
Epithelial Cells/*metabolism
Epithelial Cells/*radiation effects
Cell Line ; Dose-Response Relationship, Radiation ; HeLa Cells ; Humans ; Radiation Dosage
Substance Nomenclature:
SY7Q814VUP (Calcium)
Entry Date(s):
Date Created: 20080904 Date Completed: 20081016 Latest Revision: 20131121
Update Code:
20240104
DOI:
10.1667/RR1270.1
PMID:
18763861
Czasopismo naukowe
Intracellular calcium is an important second messenger that regulates many cell functions. Recent studies have shown that calcium ions can also regulate the cellular responses to ionizing radiation. However, previous data are restricted to cells treated with low-LET radiations (X rays, gamma rays and beta particles). In this work, we investigated the calcium levels in cells exposed to heavy-ion radiation of high LET. The experiments were performed at the single ion hit facility of the GSI heavy-ion microprobe. Using a built-in online calcium imaging system, the intracellular calcium concentrations were examined in HeLa cells and human foreskin fibroblast AG1522-D cells before and after irradiation with 4.8 MeV/nucleon carbon or argon ions. Although the experiment was sensitive enough to detect the calcium response to other known stimuli, no response to heavy-ion radiation was found in these two cell types. We also found that heavy-ion radiation has no impact on calcium oscillation induced by hypoxia stress in fibroblast cells.

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