Literature DB >> 11526954

Ion channels in cultured microglia.

W Walz1, L K Bekar.   

Abstract

Inward and, depending on activation state, outward potassium currents are the dominant ion channels in microglial cells in culture. During transition between resting and activated phases, there is also an upregulated expression of stretch/swelling-activated chloride currents. Pharmacological blockade of the specific potassium channels does not prevent the transition, whereas blockade of chloride channels does, suggesting that this current may be involved in phase changes. Interestingly, this chloride current is far less studied than the potassium currents with regard to the different microglial phases. One puzzling finding when studying microglial state is that despite changes in current densities and membrane oscillations during transition, there is no evidence of an accompanying change in membrane potential. In other cells of the immune system, membrane oscillations and alterations in membrane potential are correlated with transitions in cellular phases. This discrepancy in microglia may be a result of the fact that almost all ion channel and membrane potential studies in culture are undertaken with concomitant dialysis of cytoplasm with pipette solution. Further complicating matters is that the few studies that use microglia in situ, find fundamental differences in ion channel current patterns of "resting" microglia as well as different temporal changes to pathological events or stimuli.

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Year:  2001        PMID: 11526954     DOI: 10.1002/jemt.1117

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  6 in total

1.  Protein 4.1 G localizes in rodent microglia.

Authors:  Nobuhiko Ohno; Nobuo Terada; Junya Tanaka; Akiko Yokoyama; Hisashi Yamakawa; Yasuhisa Fujii; Takeshi Baba; Osamu Ohara; Shinichi Ohno
Journal:  Histochem Cell Biol       Date:  2005-09-24       Impact factor: 4.304

Review 2.  Transient Receptor Potential Channels in Microglia: Roles in Physiology and Disease.

Authors:  Santiago Echeverry; María Juliana Rodriguez; Yolima P Torres
Journal:  Neurotox Res       Date:  2016-06-03       Impact factor: 3.911

3.  HIV-1 gp120 enhances outward potassium current via CXCR4 and cAMP-dependent protein kinase A signaling in cultured rat microglia.

Authors:  Changshui Xu; Jianuo Liu; Lina Chen; Shangdong Liang; Nobutaka Fujii; Hirokazu Tamamura; Huangui Xiong
Journal:  Glia       Date:  2011-03-24       Impact factor: 7.452

4.  Lipopolysaccharide-induced down-regulation of Ca2+ release-activated Ca2+ currents (I CRAC) but not Ca2+-activated TRPM4-like currents (I CAN) in cultured mouse microglial cells.

Authors:  Andreas Beck; Reinhold Penner; Andrea Fleig
Journal:  J Physiol       Date:  2007-11-08       Impact factor: 5.182

5.  Involvement of Kv1.3 and p38 MAPK signaling in HIV-1 glycoprotein 120-induced microglia neurotoxicity.

Authors:  J Liu; C Xu; L Chen; P Xu; H Xiong
Journal:  Cell Death Dis       Date:  2012-01-19       Impact factor: 8.469

6.  HIV-1 Tat protein increases microglial outward K(+) current and resultant neurotoxic activity.

Authors:  Jianuo Liu; Peng Xu; Cory Collins; Han Liu; Jingdong Zhang; James P Keblesh; Huangui Xiong
Journal:  PLoS One       Date:  2013-05-30       Impact factor: 3.240

  6 in total

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