Plasma membrane localization and function of TRPC1 is dependent on its interaction with β-tubulin in retinal epithelium cells

Sunitha Bollimuntha, Eric Cornatzer, Brij B. Singh

Research output: Contribution to journalArticle

39 Scopus citations


Mammalian homologues of the Drosophila canonical Transient Receptor Potential (TRPC) protein have been proposed to encode the store-operated Ca 2+ influx (SOC) channel(s). This study examines the role of TRPC1 in the SOC mechanism of retinal cells, htrpc1 transcript was detected in bovine retinal and in human adult retinal pigment epithelial (ARPE) cells. Western blot analysis also confirmed the expression of TRPC1 protein in neuronal cells including retina and ARPE cells. To determine the role of TRPC1 protein in retinal cells, TRPC1 was recombinantly expressed in ARPE cells and changes in intracellular Ca2+ were analyzed. ARPE cells stably transfected with htrp1 cDNA displayed 2-fold higher Ca2+ influx with no significant increase in the basal influx. Consistent with this the overexpressed TRPC1 protein was localized in the plasma membrane region of ARPE cells. Interestingly, both bovine retinal tissues and ARPE cells showed that TRPC1 protein co-localizes and could be co-immunoprecipitated with β-tubulin. Disruption of tubulin by colchicine significantly decreased both plasma membrane staining of the TRPC1 protein and Ca2+ influx in ARPE cells. These results suggest that TRPC1 channel protein is expressed in retinal cells, further, targeting/retention of the TRPC1 protein to the plasma membrane in retinal cells is mediated via its interaction with β-tubulin.

Original languageEnglish (US)
Pages (from-to)163-170
Number of pages8
JournalVisual Neuroscience
Issue number2
StatePublished - Mar 1 2005



  • Retina
  • Store-operated calcium entry
  • Trafficking
  • Transient receptor potential protein
  • β-tubulin

ASJC Scopus subject areas

  • Physiology
  • Sensory Systems

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