Physiological properties of retinal Müller glial cells from the cynomolgus monkey, Macaca fascicularis - A comparison to human Müller cells

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Thomas Pannicke - , Leipzig University (Author)
  • Bernd Biedermann - , Leipzig University (Author)
  • Ortrud Uckermann - , University Hospital Leipzig, Leipzig University (Author)
  • Michael Weick - , Leipzig University (Author)
  • Andreas Bringmann - , Leipzig University (Author)
  • Sebastian Wolf - , Leipzig University, Inselspital University Hospital Bern (Author)
  • Peter Wiedemann - , Leipzig University (Author)
  • Gunnar Habermann - , Covance Laboratories GmbH (Author)
  • Eberhard Buse - , Covance Laboratories GmbH (Author)
  • Andreas Reichenbach - , Leipzig University (Author)

Abstract

Retinae from rabbits and laboratory rodents are often used as 'models' of the human retina, although there are anatomical differences. To test whether monkey eyes provide a better model, a physiological study of Müller glial cells was performed comparing isolated cells and retinal wholemounts from the cynomolgus monkey, Macaca fascicularis and from man. The membrane conductance of Müller cells from both species was dominated by inward and outward K + currents. Cells displayed glutamate uptake currents and responded to nucleotides by intracellular Ca2+ increases. However, there were also species differences, such as a lack of GABAA receptors and of Ca2+-dependent K+ currents in monkey cells. Thus, the use of Müller cells from cynomolgus monkeys may be advantageous for investigating a few specific properties; in general, monkey cells are no more similar to human cells than those from standard laboratory animals.

Details

Original languageEnglish
Pages (from-to)1781-1791
Number of pages11
JournalVision Research
Volume45
Issue number14
Publication statusPublished - Jun 2005
Peer-reviewedYes
Externally publishedYes

External IDs

PubMed 15797768

Keywords

ASJC Scopus subject areas

Keywords

  • Ca microfluorimetry, K currents, Membrane channels, P2 receptors, Patch-clamp methodology