scholarly journals Calcium- and polyphosphate-containing acidic granules of sea urchin eggs are similar to acidocalcisomes, but are not the targets for NAADP

2010 ◽  
Vol 429 (3) ◽  
pp. 485-495 ◽  
Author(s):  
Isabela B. Ramos ◽  
Kildare Miranda ◽  
Douglas A. Pace ◽  
Katherine C. Verbist ◽  
Fu-Yang Lin ◽  
...  

Acidocalcisomes are acidic calcium-storage compartments described from bacteria to humans and characterized by their high content in poly P (polyphosphate), a linear polymer of many tens to hundreds of Pi residues linked by high-energy phosphoanhydride bonds. In the present paper we report that millimolar levels of short-chain poly P (in terms of Pi residues) and inorganic PPi are present in sea urchin extracts as detected using 31P-NMR, enzymatic determinations and agarose gel electrophoresis. Poly P was localized to granules randomly distributed in the sea urchin eggs, as shown by labelling with the poly-P-binding domain of Escherichia coli exopolyphosphatase. These granules were enriched using iodixanol centrifugation and shown to be acidic and to contain poly P, as determined by Acridine Orange and DAPI (4′,6′-diamidino-2-phenylindole) staining respectively. These granules also contained large amounts of calcium, sodium, magnesium, potassium and zinc, as detected by X-ray microanalysis, and bafilomycin A1-sensitive ATPase, pyrophosphatase and exopolyphosphatase activities, as well as Ca2+/H+ and Na+/H+ exchange activities, being therefore similar to acidocalcisomes described in other organisms. Calcium release from these granules induced by nigericin was associated with poly P hydrolysis. Although NAADP (nicotinic acid–adenine dinucleotide phosphate) released calcium from the granule fraction, this activity was not significantly enriched as compared with the NAADP-stimulated calcium release from homogenates and was not accompanied by poly P hydrolysis. GPN (glycyl-L-phenylalanine-naphthylamide) released calcium when added to sea urchin homogenates, but was unable to release calcium from acidocalcisome-enriched fractions, suggesting that these acidic stores are not the targets for NAADP.

1998 ◽  
Vol 242 (1) ◽  
pp. 328-340 ◽  
Author(s):  
Shyh-Jye Lee ◽  
Patrick J. Madden ◽  
Sheldon S. Shen

2000 ◽  
Vol 92 (3-4) ◽  
pp. 197-204 ◽  
Author(s):  
Antony Galione ◽  
Sandip Patel ◽  
Grant C. Churchill

2000 ◽  
Vol 218 (2) ◽  
pp. 206-219 ◽  
Author(s):  
Yama A. Abassi ◽  
David J. Carroll ◽  
Andrew F. Giusti ◽  
Robert J. Belton ◽  
Kathy R. Foltz

1992 ◽  
Vol 116 (5) ◽  
pp. 1111-1121 ◽  
Author(s):  
S M McPherson ◽  
P S McPherson ◽  
L Mathews ◽  
K P Campbell ◽  
F J Longo

We have used an antibody against the ryanodine receptor/calcium release channel of skeletal muscle sarcoplasmic reticulum to localize a calcium release channel in sea urchin eggs. The calcium release channel is present in less than 20% of immature oocytes, where it does not demonstrate a specific cytoplasmic localization, while it is confined to the cortex of all mature eggs examined. This is in contrast to the cortical and subcortical localization of calsequestrin in mature and immature eggs. Immunolocalization of the calcium release channel reveals a cortical reticulum or honeycomb staining network that surrounds cortical granules and is associated with the plasma membrane. The network consists of some immunoreactive electron-dense material coating small vesicles and elongate cisternae of the endoplasmic reticulum. The fluorescent reticular staining pattern is lost when egg cortices are treated with agents known to affect sarcoplasmic reticulum calcium release and induce cortical granule exocytosis (ryanodine, calcium, A-23187, and caffeine). An approximately 380-kD protein of sea urchin egg cortices is identified by immunoblot analysis with the ryanodine receptor antibody. These results demonstrate: (a) the presence of a ryanodine-sensitive calcium release channel that is located within the sea urchin egg cortex; (b) an altered calcium release channel staining pattern as a result of treatments that initiate the cortical granule reaction; and (c) a spatial and functional dichotomy of the ER which may be important in serving different roles in the mobilization of calcium at fertilization.


1988 ◽  
Vol 63 (S1) ◽  
pp. 3-3a
Author(s):  
Isabelle Gillot ◽  
Brigitte Ciapa ◽  
Guy Renzis ◽  
Patrick Payan ◽  
Christian Sardet ◽  
...  

1996 ◽  
Vol 180 (1) ◽  
pp. 324-335 ◽  
Author(s):  
Shyh-Jye Lee ◽  
Leslie Christenson ◽  
Tracie Martin ◽  
Sheldon S. Shen

Zygote ◽  
1993 ◽  
Vol 1 (1) ◽  
pp. 35-42 ◽  
Author(s):  
Alex McDougall ◽  
Isabelle Gillot ◽  
Michael Whitaker

SummaryThe fertilisation calcium wave in sea urchin eggs triggers the onset of development. The wave is an explosive increase in intracellular free calcium concentration that begins at the point of sperm entry and crosses the egg in about 20 s. Thimerosal is a sulphydryl reagent that sensitises calcium release from intracellular stores in a variety of cell types. Treatment of unfertilised eggs with thimerosal causes a slow increase that results eventually in a large, spontaneous calcium transient and egg activation. At shorter times after thimerosal treatment, egg activation and the calcium transient can be triggered by calcium influx through voltage-gated calcium channels, a form of calcium-induced/calcium release (CICR). Thimerosal treatment also reduces the latency of the fertilisation calcium response and increases the velocity of the fertilisation wave. These results indicate that thimerosal can unmask CICR in sea urchin eggs and suggest that the ryanodine receptor channel based CICR may contribute to explosive calcium release during the fertilisation wave.


1965 ◽  
Vol 26 (4) ◽  
pp. 534 ◽  
Author(s):  
Bhashini Rao ◽  
R. T. Hinegardner

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