Detailed Information on Publication Record
2016
Transient suppression of gap junctional intercellular communication after exposure to 100-nanosecond pulsed electric fields
STEUER, Anna, Anke SCHMIDT, Petra LABOHÁ, Pavel BABICA, Juergen F. KOLB et. al.Basic information
Original name
Transient suppression of gap junctional intercellular communication after exposure to 100-nanosecond pulsed electric fields
Authors
STEUER, Anna (276 Germany), Anke SCHMIDT (276 Germany), Petra LABOHÁ (203 Czech Republic, belonging to the institution), Pavel BABICA (203 Czech Republic, guarantor, belonging to the institution) and Juergen F. KOLB (276 Germany)
Edition
Bioelectrochemistry, SWITZERLAND, Elsevier, 2016, 1567-5394
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10405 Electrochemistry
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.346
RIV identification code
RIV/00216224:14310/16:00093524
Organization unit
Faculty of Science
UT WoS
000383523800005
Keywords in English
GJIC; nsPEF; Connexin 43; Cx43; MAP kinase; Actin
Tags
International impact, Reviewed
Změněno: 14/4/2017 21:10, Ing. Andrea Mikešková
Abstract
V originále
Gap junctional intercellular communication (GJIC) is an important mechanism that is involved and affected in many diseases and injuries. So far, the effect of nanosecond pulsed electric fields (nsPEFs) on the communication between cells was not investigated. An in vitro approach is presented with rat liver epithelial WB-F344 cells grown and exposed in a monolayer. In order to observe sub-lethal effects, cells were exposed to pulsed electric fields with a duration of 100 ns and amplitudes between 10 and 20 kV/cm. GJIC strongly decreased within 15 min after treatment but recovered within 24 h. Gene expression of Cx43 was significantly decreased and associated with a reduced total amount of Cx43 protein. In addition, MAP kinases p38 and Erk1/2, involved in Cx43 phosphorylation, were activated and Cx43 became hyperphosphorylated. Immunofluorescent staining of Cx43 displayed the disassembly of gap junctions. Further, a reorganization of the actin cytoskeleton was observed whereas tight junction protein ZO-1 was not significantly affected. All effects were field- and time-dependent and most pronounced within 30 to 60 min after treatment. A better understanding of a possible manipulation of GJIC by nsPEFs might eventually offer a possibility to develop and improve treatments.
Links
LM2015051, research and development project |
| ||
LO1214, research and development project |
|