Source:http://linkedlifedata.com/resource/pubmed/id/17349690
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2007-10-2
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pubmed:abstractText |
Ca2+ is a fundamental intracellular signal that mediates a variety of disparate physiological functions often in the same cell. Ca2+ signals span a wide range of spatial and temporal scales, which endow them with the specificity required to induce defined cellular functions. Furthermore, Ca2+ signaling is highly plastic as it is modulated dynamically during normal physiological development and under pathological conditions. However, the molecular mechanisms underlying Ca2+ signaling differentiation during cellular development remain poorly understood. Oocyte maturation in preparation for fertilization provides an exceptionally well-suited model to elucidate Ca2+ signaling regulation during cellular development. This is because a Ca2+ signal with specialized spatial and temporal dynamics is universally essential for egg activation at fertilization. Here we use mathematical modeling to define the critical determinants of Ca2+ signaling differentiation during oocyte maturation. We show that increasing IP3 receptor (IP3R) affinity replicates both elementary and global Ca2+ dynamics observed experimentally following oocyte maturation. Furthermore, our model reveals that because of the Ca2+ dependency of both SERCA and the IP3R, increased IP3R affinity shifts the system's equilibrium to a new steady state of high cytosolic Ca2+, which is essential for fertilization. Therefore our model provides unique insights into how relatively small alterations of the basic molecular mechanisms of Ca2+ signaling components can lead to dramatic alterations in the spatio-temporal properties of Ca2+ dynamics.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0143-4160
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
556-64
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pubmed:meshHeading |
pubmed-meshheading:17349690-Algorithms,
pubmed-meshheading:17349690-Animals,
pubmed-meshheading:17349690-Calcium,
pubmed-meshheading:17349690-Calcium Signaling,
pubmed-meshheading:17349690-Cell Differentiation,
pubmed-meshheading:17349690-Female,
pubmed-meshheading:17349690-Inositol 1,4,5-Trisphosphate Receptors,
pubmed-meshheading:17349690-Models, Biological,
pubmed-meshheading:17349690-Oocytes,
pubmed-meshheading:17349690-Plasma Membrane Calcium-Transporting ATPases,
pubmed-meshheading:17349690-Xenopus
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pubmed:year |
2007
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pubmed:articleTitle |
Modeling Ca2+ signaling differentiation during oocyte maturation.
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pubmed:affiliation |
Department of Physics and Astronomy and Quantitative Biology Institute, Ohio University, Athens, OH 45701, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, N.I.H., Extramural
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