PIP2 activates TRPV5 and releases its inhibition by intracellular Mg2+

Jason Lee, Seung Kuy Cha, Tie Jun Sun, Chou Long Huang

Research output: Contribution to journalArticle

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Abstract

The transient receptor potential type V5 channel (TRPV5) is a Ca 2+-selective TRP channel important for epithelial Ca2+ transport. Intracellular Mg2+ causes a fast voltage-dependent block of the TRPV5 channel by binding to the selectivity filter. Here, we report that intracellular Mg2+ binding to the selectivity filter of TRPV5 also causes a slower reversible conformational change leading to channel closure. We further report that PIP2 activates TRPV5. Activation of TRPV5 by PIP2 is independent of Mg2+. Yet, PIP2 decreases sensitivity of the channel to the Mg2+-induced slow inhibition. Mutation of aspartate-542, a critical Mg2+-binding site in the selectivity filter, abolishes Mg2+-induced slow inhibition. PIP2 has no effects on Mg2+-induced voltage-dependent block. Thus, PIP2 prevents the Mg2+-induced conformational change without affecting Mg2+ binding to the selectivity filter. Hydrolysis of PIP2 via receptor activation of phospholipase C sensitizes TRPV5 to the Mg2+-induced slow inhibition. These results provide a novel mechanism for regulation of TRP channels by phospholipase C-activating hormones via alteration of the sensitivity to intracellular Mg 2+.

Original languageEnglish (US)
Pages (from-to)439-451
Number of pages13
JournalJournal of General Physiology
Volume126
Issue number5
DOIs
StatePublished - 2005

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Transient Receptor Potential Channels
Type C Phospholipases
Aspartic Acid
Hydrolysis
Binding Sites
Hormones
Mutation

ASJC Scopus subject areas

  • Physiology

Cite this

PIP2 activates TRPV5 and releases its inhibition by intracellular Mg2+. / Lee, Jason; Cha, Seung Kuy; Sun, Tie Jun; Huang, Chou Long.

In: Journal of General Physiology, Vol. 126, No. 5, 2005, p. 439-451.

Research output: Contribution to journalArticle

Lee, Jason ; Cha, Seung Kuy ; Sun, Tie Jun ; Huang, Chou Long. / PIP2 activates TRPV5 and releases its inhibition by intracellular Mg2+. In: Journal of General Physiology. 2005 ; Vol. 126, No. 5. pp. 439-451.
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