Intracellular calcium stores modulation in lymph vessels depends on wall stretch

1998 ◽  
Vol 76 (4) ◽  
pp. 367-372 ◽  
Author(s):  
D J Atchison ◽  
H Rodela ◽  
M G Johnston

We studied the effect of intracellular calcium stores modulation on the ability of lymph vessels to propel fluid in a preparation of actively contracting isolated bovine mesenteric lymph vessels. Vessels were cannulated at each end, placed in a temperature-controlled organ bath, and circulated with oxygenated Krebs solution. Vessel wall tension (transmural pressure) was changed by raising the height of the fluid-filled reservoir and outflow catheters appropriately. When transmural pressure was set and maintained at 6 cmH2O (1 cmH2O = 98.1 Pa), caffeine (10-3 M), ryanodine (10-7 M), and cyclopiazonic acid (CPA; 7 x 10-6 M) inhibited lymphatic pumping. We also studied the effect of these agents on the relationship between lymph pump activity and transmural pressure, a relationship normally described by a bell-shaped curve. When transmural pressure was increased at 5-min intervals, the magnitude of inhibition by caffeine (10-3 M) and CPA (7 x 10-6 M) was greater than when transmural pressure was held constant. Ryanodine, on the other hand, had no effect on lymphatic contractility when transmural pressure was manipulated. The ryanodine results suggest the existence of an interaction between vessel wall stretch and intracellular calcium stores modulation that is not seen with caffeine or CPA.Key words: caffeine, ryanodine,cyclopiazonic acid, calcium-induced calcium release.

Cell Calcium ◽  
1998 ◽  
Vol 23 (1) ◽  
pp. 43-52 ◽  
Author(s):  
LászlóG. Mészáros ◽  
Alexandra Zahradnikova ◽  
Pompeo Volpe

1999 ◽  
Vol 77 (7) ◽  
pp. 520-528 ◽  
Author(s):  
Audrey Petit ◽  
Catherine Bleicher ◽  
Benoît T Lussier

In rat pituitary somatotrophs, the stimulation of growth hormone secretion by growth hormone-releasing hormone (GHRH) is a Ca2+-dependent event involving Ca2+ influx. The presence of calcium-induced calcium release (CICR) Ca2+ stores has been suggested in these cells. The aim of our study was to demonstrate the presence of CICR stores in rat somatotrophs and to determine their function in GHRH Ca2+ signalling. To this end we measured cytosolic free Ca2+ concentration ([Ca2+]i), using indo-1 in purified rat somatotrophs in primary culture, while altering intracellular Ca2+ stores. Ionomycin (10 µM) or 4-bromo-A23187 (10 µM), used to mobilise organelle-bound Ca2+, raised [Ca2+]i in the absence of extracellular Ca2+. Caffeine (5 to 50 mM), used to mobilise Ca2+ from CICR stores, transiently raised [Ca2+]i in 65% of cells tested. The response to 40 mM caffeine was abolished when Ca2+ stores were depleted, with 1 µM thapsigargin or with 10 µM ryanodine. All cells that responded to 40 mM caffeine responded to 10 nM GHRH. The [Ca2+]i response to 10 nM GHRH was reversible and repeatable. However, the second response was 38% smaller than the first. Ryanodine treatment abolished the reduction in the second [Ca2+]i response, while thapsigargin increased the reduction by 67%. We conclude that rat somatotrophs possess CICR Ca2+ stores and that they account for 30-35% of the GHRH-induced increase in [Ca2+]i, and that their partial depletion is involved in somatotroph desensitization.Key words: somatotrophs, growth hormone-releasing hormone, intracellular calcium, calcium stores, calcium-induced calcium release.


1996 ◽  
Vol 271 (9) ◽  
pp. 4601-4604 ◽  
Author(s):  
Ludwig Missiaen ◽  
Humbert De Smedt ◽  
Jan B. Parys ◽  
Ilse Sienaert ◽  
Sara Vanlingen ◽  
...  

2000 ◽  
Vol 115 (3) ◽  
pp. 339-346 ◽  
Author(s):  
Mary D. Womack ◽  
Jeffery W. Walker ◽  
Kamran Khodakhah

Cerebellar Purkinje neurons demonstrate a form of synaptic plasticity that, in acutely prepared brain slices, has been shown to require calcium release from the intracellular calcium stores through inositol trisphosphate (InsP3) receptors. Similar studies performed in cultured Purkinje cells, however, find little evidence for the involvement of InsP3 receptors. To address this discrepancy, the properties of InsP3- and caffeine-evoked calcium release in cultured Purkinje cells were directly examined. Photorelease of InsP3 (up to 100 μM) from its photolabile caged analogue produced no change in calcium levels in 70% of cultured Purkinje cells. In the few cells where a calcium increase was detected, the response was very small and slow to peak. In contrast, the same concentration of InsP3 resulted in large and rapidly rising calcium responses in all acutely dissociated Purkinje cells tested. Similar to InsP3, caffeine also had little effect on calcium levels in cultured Purkinje cells, yet evoked large calcium transients in all acutely dissociated Purkinje cells tested. The results demonstrate that calcium release from intracellular calcium stores is severely impaired in Purkinje cells when they are maintained in culture. Our findings suggest that cultured Purkinje cells are an unfaithful experimental model for the study of the role of calcium release in the induction of cerebellar long term depression.


2004 ◽  
Vol 88 (6) ◽  
pp. 1361-1372 ◽  
Author(s):  
Yaxiong Yang ◽  
Gregory A. Kinney ◽  
William J. Spain ◽  
John C. S. Breitner ◽  
David G. Cook

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