Ion channels in the RPE

Research output: Contribution to journalReview articleContributedpeer-review

Contributors

  • Sönke Wimmers - , University Hospital Hamburg Eppendorf (Author)
  • Mike O. Karl - , University Hospital Hamburg Eppendorf (Author)
  • Olaf Strauss - , University Hospital Hamburg Eppendorf (Author)

Abstract

In close interaction with photoreceptors, the retinal pigment epithelium (RPE) plays an essential role for visual function. The analysis of RPE functions, specifically ion channel functions, provides a basis to understand many degenerative diseases of the retina. The invention of the patch-clamp technique significantly improved the knowledge of ion channel structure and function, which enabled a new understanding of cell physiology and patho-physiology of many diseases. In this review, ion channels identified in the RPE will be described in terms of their specific functional role in RPE physiology. The RPE expresses voltage- and ligand-gated K+, Cl-, and Ca2+-conducting channels. K+ and Cl- channels are involved in transepithelial ion transport and volume regulation. Voltage-dependent Ca2+ channels act as regulators of secretory activity, and ligand-gated cation channels contribute to RPE function by providing driving forces for ion transport or by influencing intracellular Ca2+ homoeostasis. Collectively, activity of these ion channels determines the physiology of the RPE and its interaction with photoreceptors. Furthermore, changes in ion channel function, such as mutations in ion channel genes or a changed regulation of ion channel activity, have been shown to lead to degenerative diseases of the retina. Increasing knowledge about the properties of RPE ion channels has not only provided a new understanding of RPE function but has also provided greater understanding of RPE function in health and disease.

Details

Original languageEnglish
Pages (from-to)263-301
Number of pages39
JournalProgress in retinal and eye research
Volume26
Issue number3
Publication statusPublished - May 2007
Peer-reviewedYes
Externally publishedYes

External IDs

Scopus 33947639553
PubMed 17258931

Keywords