By CIBA Foundation Symposium
Popular individuals offer entire assurance of calcium gradients, waves and oscillations in diversified platforms. Discusses the mechanisms beginning and maintaining calcium waves and their function in mobile functionality. Describes stories utilizing the newest recommendations for measuring calcium ion gradients together with chemiluminescent signs.
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Additional resources for Ciba Foundation Symposium 188 - Calcium Waves, Gradients and Oscillations
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Could you elaborate on what is special about that particular point? Thomas: The distribution of InsP3-sensitive pools does not seem to be the explanation. My hypothesis is that this site contains the InsP3-generating machinery, the phospholipase C or the hormone receptor. The liver has a relatively high standing concentration of InsP3 such that a small additional stimulation of the InsP3 receptor is enough to initiate the Ca2+ waves. My idea, and I think Tobias Meyer would probably disagree with this, is that there’s an area of the cell which has all the signal transduction mechanisms and perhaps Ca2+ pools that are more sensitive to InsP3 and/or a slightly higher concentration of InsP3.
Therefore, you are getting a push in the system. Ca2 activates the dehydrogenase, and NADH levels are increased, which will push the respiratory chain and more ATP will be made. Fay: With L. Loew, we have measured mitochondrial membrane potential with dyes in cultured neurons and found that mitochondria become depolarized in response to an increase in cytosolic [ C a 2 + ] (Loew et a1 1994). The + + Subcellular organization of hepatic Ca2+ signals 41 predominant effect in the cells is that Ca2+ influx causes a fall in mitochondrial membrane potential rather than stimulation of the electron transport chain, which might be expected to increase membrane potential.
In this preparation, GTP increases the Mn2+-quenchable pool size by adding a slowly accessible pool without increasing the initial rate of quenching (Hajnoczky et al 1994). Significantly, this effect is blocked by cytochalasin B, suggesting a role for the cytoskeleton in the process as it occurs in the permeabilized hepatocyte. Furthermore, addition of GTP can reverse the functional fragmentation of Ca2+ stores that occurs when the cytoskeleton of attached permeabilized hepatocytes is disrupted by prolonged cold treatment.