Imaging the hierarchical Ca2+ signalling system in HeLa cells.

1. Confocal microscopy was used to investigate hormone‐induced subcellular Ca2+ release signals from the endoplasmic reticulum (ER) in a prototype non‐excitable cell line (HeLa cells). 2. Histamine application evoked two types of elementary Ca2+ signals: (i) Ca2+ blips arising from single ER Ca2+ release channels (amplitude, 30 nM; lateral spreading, 1.3 microns); (ii) Ca2+ puffs resulting from the concerted activation of several Ca2+ blips (amplitude, 170 nM; spreading, 4 microns). 3. Ca2+ waves in the HeLa cells arose from a variable number of initiation sites, but for individual cells, the number and subcellular location of the initiation sites were constant. The kinetics and amplitude of global Ca2+ signals were directly proportional to the number of initiation sites recruited. 4. Reduction of the feedback inherent in intracellular Ca2+ release caused saltatoric Ca2+ waves, revealing the two principal steps underlying wave propagation: diffusion and regeneration. Threshold stimulation evoked abortive Ca2+ waves, caused by the limited recruitment of Ca2+ puffs. 5. The hierarchy of Ca2+ signalling events, from fundamental levels (blips) to intermediate levels (puffs) to Ca2+ waves, is a prototype for Ca2+ signal transduction for non‐excitable cells, and is also analogous to the Ca2+ quarks, Ca2+ sparks and Ca2+ waves in cardiac muscle cells.

[1]  M. Rubart,et al.  Relaxation of Arterial Smooth Muscle by Calcium Sparks , 1995, Science.

[2]  P. Lipp,et al.  Modulation of Ca2+ release in cultured neonatal rat cardiac myocytes. Insight from subcellular release patterns revealed by confocal microscopy. , 1994, Circulation research.

[3]  M. Berridge,et al.  Inositol Trisphosphate and Calcium Signaling , 1995, Annals of the New York Academy of Sciences.

[4]  I. Parker,et al.  Regenerative release of calcium from functionally discrete subcellular stores by inositol trisphosphate , 1991, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[5]  I. Parker,et al.  Ca2+ transients associated with openings of inositol trisphosphate‐gated channels in Xenopus oocytes. , 1996, The Journal of physiology.

[6]  Martin D. Bootman,et al.  The elemental principles of calcium signaling , 1995, Cell.

[7]  W. Lederer,et al.  Calcium sparks: elementary events underlying excitation-contraction coupling in heart muscle. , 1993, Science.

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

[9]  E Neher,et al.  Mobile and immobile calcium buffers in bovine adrenal chromaffin cells. , 1993, The Journal of physiology.

[10]  P. Lipp,et al.  Submicroscopic calcium signals as fundamental events of excitation‐‐contraction coupling in guinea‐pig cardiac myocytes. , 1996, The Journal of physiology.

[11]  C W Balke,et al.  Local calcium transients triggered by single L-type calcium channel currents in cardiac cells. , 1995, Science.

[12]  C. Petersen,et al.  Calcium and hormone action. , 1994, Annual review of physiology.

[13]  M. Berridge,et al.  Subcellular Ca2+ signals underlying waves and graded responses in HeLa cells , 1996, Current Biology.

[14]  L. Blatter,et al.  Imaging elementary events of calcium release in skeletal muscle cells. , 1995, Science.

[15]  D. Clapham,et al.  Calcium release from the nucleus by InsP3 receptor channels , 1995, Neuron.

[16]  M. G. Klein,et al.  Two mechanisms of quantized calcium release in skeletal muscle , 1996, Nature.

[17]  P. Lipp,et al.  Subcellular features of calcium signalling in heart muscle: what do we learn? , 1995, Cardiovascular research.

[18]  M. Berridge Inositol trisphosphate and calcium signalling , 1993, Nature.

[19]  M. Berridge,et al.  Smoothly graded Ca2+ release from inositol 1,4,5-trisphosphate-sensitive Ca2+ stores. , 1994, The Journal of biological chemistry.