Ca2+ blinks: Rapid nanoscopic store calcium signaling

  1. Didier X. P. Brochet*,
  2. Dongmei Yang*,,
  3. Alessandro Di Maio,
  4. W. Jonathan Lederer§,
  5. Clara Franzini-Armstrong, and
  6. Heping Cheng*,,
  1. *Laboratory of Cardiovascular Science, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224; Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, PA 19104; §Medical Biotechnology Center, University of Maryland Biotechnology Institute, Baltimore, MD 21201; and Institute of Molecular Medicine and National Laboratory of Biomembrane and Membrane Biotechnology, Peking University, Beijing 100871, China
  1. Contributed by Clara Franzini-Armstrong, January 4, 2005

Abstract

Luminal Ca2+ in the endoplasmic and sarcoplasmic reticulum (ER/SR) plays an important role in regulating vital biological processes, including store-operated capacitative Ca2+ entry, Ca2+-induced Ca2+ release, and ER/SR stress-mediated cell death. We report rapid and substantial decreases in luminal [Ca2+], called “Ca2+ blinks,” within nanometer-sized stores (the junctional cisternae of the SR) during elementary Ca2+ release events in heart cells. Blinks mirror small local increases in cytoplasmic Ca2+,orCa2+ sparks, but changes of [Ca2+] in the connected free SR network were below detection. Store microanatomy suggests that diffusional strictures may account for this paradox. Surprisingly, the nadir of the store depletion trails the peak of the spark by about 10 ms, and the refilling of local store occurs with a rate constant of 35 s-1, which is ≈6-fold faster than the recovery of local Ca2+ release after a spark. These data suggest that both local store depletion and some time-dependent inhibitory mechanism contribute to spark termination and refractoriness. Visualization of local store Ca2+ signaling thus broadens our understanding of cardiac store Ca2+ regulation and function and opens the possibility for local regulation of diverse store-dependent functions.

Footnotes

  • To whom correspondence may be addressed. E-mail: yangd1{at}grc.nia.nih.gov or chengp{at}grc.nia.nih.gov.

  • Abbreviations: ER, endoplasmic reticulum; SR, sarcoplasmic reticulum; jSR, junctional SR; fSR, free SR; RyR, ryanodine receptor; FWHM, full width at half maximum.

  • Freely available online through the PNAS open access option.

« Previous | Next Article »Table of Contents