Cyclic ADP-ribose activates caffeine-sensitive calcium channels from sea urchin egg microsomes

Ferez C.F.; Marengo, J.J.; Bull, R; Hidalgo C.

Keywords: magnesium, sequence, ruthenium, acid, transport, animals, cell, chloride, ryanodine, caffeine, channel, calcium, sea, channels, ribose, potassium, heparin, bilayers, microsomes, level, ovum, adenosine, indicators, article, 1,4,5-trisphosphate, phosphatase, red, sulfonamides, reagents, calmodulin, lipid, microsome, echinoidea, inositol, animal, amino, priority, cyclic, nonhuman, journal, Animalia, triphosphate, reticulum, and, endoplasmic, urchin, Urchins, Diphosphate, ADP-Ribose

Abstract

Adenosine 5'-cyclic diphosphoribose [cyclic ADP-ribose (cADPR)], a metabolite of NAD+ that promotes Ca2+ release from sea urchin egg homogenates and microsomal fractions, has been proposed to act as an endogenous agonist of Ca2+ release in sea urchin eggs. We describe experiments showing that a microsomal fraction isolated from Tetrapigus nyger sea urchin eggs displayed Ca2+-selective single channels with conductances of 155.0 ± 8.0 pS in asymmetric Cs+ solutions and 47.5 ± 1.1 pS in asymmetric Ca2+ solutions. These channels were sensitive to stimulation by Ca2+, ATP, and caffeine, but not inositol 1,4,5-trisphosphate, and were inhibited by ruthenium red. The channels were also activated by cADP-ribose in a Ca2+-dependent fashion. Calmodulin and Mg2+, but not heparin, modulated channel activity in the presence of cADP-ribose. We propose that these Ca2+ channels constitute the intracellular Ca2+-induced Ca2+ release pathway that is activated by cADP-ribose in sea urchin eggs.

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Título de la Revista: AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volumen: 274
Número: 2 43-2
Editorial: AMER PHYSIOLOGICAL SOC
Fecha de publicación: 1998
URL: http://www.scopus.com/inward/record.url?eid=2-s2.0-0031935931&partnerID=q2rCbXpz