The probability of triggering calcium puffs is linearly related to the number of inositol trisphosphate receptors in a cluster.

Puffs are local Ca(2+) signals that arise by Ca(2+) liberation from the endoplasmic reticulum through concerted opening of tightly clustered inositol trisphosphate receptor/channels (IP(3)R). They serve both local signaling functions and trigger global Ca(2+) waves. The numbers of functional IP(3)R within clusters differ appreciably between different puff sites, and we investigated how the probability of puff occurrence varies with cluster size. We imaged puffs in SH-SY5Y cells using total internal fluorescence microscopy, and estimated cluster sizes from the magnitude of the largest puff observed at each site relative to the signal from a single channel. We find that the initial triggering rate of puffs following photorelease of IP(3), and the average frequency of subsequent repetitive puffs, vary about linearly with cluster size. These data accord well with stochastic simulations in which opening of any individual IP(3)R channel within a cluster triggers a puff via Ca(2+)-induced Ca(2+) release. An important consequence is that the signaling power of a puff site (average amount of Ca(2+) released per puff × puff frequency) varies about the square of cluster size, implying that large clusters contribute disproportionately to cellular signaling and, because of their higher puff frequency, preferentially act as pacemakers to initiate Ca(2+) waves.

[1]  J. Keizer,et al.  A single-pool inositol 1,4,5-trisphosphate-receptor-based model for agonist-stimulated oscillations in Ca2+ concentration. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[2]  Ian Parker,et al.  Localization of puff sites adjacent to the plasma membrane: functional and spatial characterization of Ca2+ signaling in SH-SY5Y cells utilizing membrane-permeant caged IP3. , 2009, Cell calcium.

[3]  Ghanim Ullah,et al.  Erratum: A simple sequential-binding model for calcium puffs [ Chaos 19, 037109 (2009) ]. , 2010 .

[4]  I. Parker,et al.  Superresolution localization of single functional IP3R channels utilizing Ca2+ flux as a readout. , 2010, Biophysical journal.

[5]  P. Jung,et al.  The role of agonist-independent conformational transformation (AICT) in IP₃ cluster behavior. , 2011, Cell calcium.

[6]  Ian Parker,et al.  Analysis of puff dynamics in oocytes: interdependence of puff amplitude and interpuff interval. , 2006, Biophysical journal.

[7]  J. Shuai,et al.  'Trigger' events precede calcium puffs in Xenopus oocytes. , 2006, Biophysical journal.

[8]  Suman Datta,et al.  Rapid ligand‐regulated gating kinetics of single inositol 1,4,5‐trisphosphate receptor Ca2+ release channels , 2007, EMBO reports.

[9]  Martin Falcke,et al.  Derivation of Ca2+ signals from puff properties reveals that pathway function is robust against cell variability but sensitive for control , 2010, Proceedings of the National Academy of Sciences.

[10]  P. Jung,et al.  Optimal ion channel clustering for intracellular calcium signaling , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[11]  D Swaminathan,et al.  A simple sequential-binding model for calcium puffs. , 2009, Chaos.

[12]  D Thomas,et al.  Hormone-evoked Elementary Ca2+ Signals Are Not Stereotypic, but Reflect Activation of Different Size Channel Clusters and Variable Recruitment of Channels within a Cluster* , 1998, The Journal of Biological Chemistry.

[13]  Ian Parker,et al.  A kinetic model of single and clustered IP3 receptors in the absence of Ca2+ feedback. , 2007, Biophysical journal.

[14]  Ian Parker,et al.  Timescales of IP(3)-evoked Ca(2+) spikes emerge from Ca(2+) puffs only at the cellular level. , 2011, Biophysical journal.

[15]  Ian Parker,et al.  Spatiotemporal patterning of IP3‐mediated Ca2+ signals in Xenopus oocytes by Ca2+‐binding proteins , 2004, The Journal of physiology.

[16]  J. Pearson,et al.  Fire-diffuse-fire model of dynamics of intracellular calcium waves. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[17]  I. Parker,et al.  Quantal puffs of intracellular Ca2+ evoked by inositol trisphosphate in Xenopus oocytes. , 1995, The Journal of physiology.

[18]  P. Jung,et al.  Endoplasmic Reticulum Remodeling Tunes IP3-Dependent Ca2+ Release Sensitivity , 2011, PloS one.

[19]  J. Marchant,et al.  Role of elementary Ca(2+) puffs in generating repetitive Ca(2+) oscillations. , 2001, The EMBO journal.

[20]  Peter Lipp,et al.  Cooking with Calcium: The Recipes for Composing Global Signals from Elementary Events , 1997, Cell.

[21]  Ian Parker,et al.  The number and spatial distribution of IP3 receptors underlying calcium puffs in Xenopus oocytes. , 2006, Biophysical journal.

[22]  Recording single-channel activity of inositol trisphosphate receptors in intact cells with a microscope, not a patch clamp , 2010 .

[23]  Martin Falcke,et al.  Clustering of IP3 receptors by IP3 retunes their regulation by IP3 and Ca2+ , 2009, Nature.

[24]  B. Schwaller,et al.  Spatiotemporal patterning of IP 3-mediated Ca 2 + signals in Xenopus oocytes by Ca 2 +-binding proteins , 2004 .

[25]  Ian Parker,et al.  Activation and co‐ordination of InsP3‐mediated elementary Ca2+ events during global Ca2+ signals in Xenopus oocytes , 1998, The Journal of physiology.

[26]  Ian Parker,et al.  Role of elementary Ca2+ puffs in generating repetitive Ca2+ oscillations , 2001 .

[27]  Don-On Daniel Mak,et al.  Inositol trisphosphate receptor Ca2+ release channels. , 2007, Physiological reviews.

[28]  Ian Parker,et al.  Ca2+ Puffs Originate from Preestablished Stable Clusters of Inositol Trisphosphate Receptors , 2009, Science Signaling.

[29]  Ian Parker,et al.  Imaging the quantal substructure of single IP3R channel activity during Ca2+ puffs in intact mammalian cells , 2009, Proceedings of the National Academy of Sciences.