2005
DOI: 10.1016/j.ceca.2004.06.010
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Calcium channels, transporters and exchangers in placenta: a review

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Cited by 119 publications
(64 citation statements)
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“…Fetal accretion of Ca 2+ increases exponentially over the last third of pregnancy, concomitant with the development of the fetal skeleton (Comar, 1956), suggesting that there is cross talk between the two processes. Data suggest that in the mouse and rat placenta, as in other epithelia, Ca 2+ transport is likely to involve three main steps (Atkinson et al, 2006;Belkacemi et al, 2005): firstly, diffusion into the trophoblast from maternal plasma down an electrochemical gradient through epithelial Ca 2+ channels of the transient receptor potential (TRP) gene family; secondly, transfer across the trophoblast cytoplasm bound to the calcium binding protein calbindin-D 9K (Glazier et al, 1992); and, thirdly, active extrusion into the fetal compartment via plasma membrane Ca 2+ -ATPase (PMCA) localized to the BM (Borke et al, 1989;Fisher et al, 1987). Over the last third of gestation, gene and protein expression for calbindin-D 9K increases markedly in both mouse and rat placenta Glazier et al, 1992;Hamilton et al, 2000;Mathieu et al, 1989) and correlates with the increase in unidirectional maternofetal 45 Ca clearance measured over the same period (Glazier et al, 1992), suggesting that transcytosolic transfer on this protein and the dynamic equilibrium between bound and free Ca 2+ in the syncytiotrophoblast might be the rate limiting step of transfer in these species.…”
Section: Ca 2+ Transportmentioning
confidence: 99%
“…Fetal accretion of Ca 2+ increases exponentially over the last third of pregnancy, concomitant with the development of the fetal skeleton (Comar, 1956), suggesting that there is cross talk between the two processes. Data suggest that in the mouse and rat placenta, as in other epithelia, Ca 2+ transport is likely to involve three main steps (Atkinson et al, 2006;Belkacemi et al, 2005): firstly, diffusion into the trophoblast from maternal plasma down an electrochemical gradient through epithelial Ca 2+ channels of the transient receptor potential (TRP) gene family; secondly, transfer across the trophoblast cytoplasm bound to the calcium binding protein calbindin-D 9K (Glazier et al, 1992); and, thirdly, active extrusion into the fetal compartment via plasma membrane Ca 2+ -ATPase (PMCA) localized to the BM (Borke et al, 1989;Fisher et al, 1987). Over the last third of gestation, gene and protein expression for calbindin-D 9K increases markedly in both mouse and rat placenta Glazier et al, 1992;Hamilton et al, 2000;Mathieu et al, 1989) and correlates with the increase in unidirectional maternofetal 45 Ca clearance measured over the same period (Glazier et al, 1992), suggesting that transcytosolic transfer on this protein and the dynamic equilibrium between bound and free Ca 2+ in the syncytiotrophoblast might be the rate limiting step of transfer in these species.…”
Section: Ca 2+ Transportmentioning
confidence: 99%
“…They are also expressed in the placenta and trophoblast and play an important role in the delivery of calcium to the foetus [189,190].Heavy metal cations, particularly lead and mercury, are potent calcium channel blockers but can also permeate these channels, gaining access to the cell [191]. The enrichment ratio and the total number of genes affected by each compound are shown after each compound name.…”
Section: Autism Genes Are Targeted By Relevant Hormones and Transmittmentioning
confidence: 99%
“…In mammalian intestine, the transcellular Ca 2+ transport system plays a crucial role in maintaining Ca 2+ homeostasis, which is a three-step process, comprising the passive entry of Ca 2+ into enterocytes via the transient receptor potential vanilloid channel type 5 or 6 (TRPV5, TRPV6); the cytosolic transfer of Ca 2+ bound to the protein calbindin D 9k (avian and other lower species' tissues contain calbindin D 28K ); and the extrusion of Ca 2+ across the basolateral membrane via Ca 2+ -ATPase (PMCA 1b) and/or a Na + -Ca 2+ exchanger (NCX 1b) (van Abel et al, 2005). A similar mechanism exists in tissues such as the kidney, uterus, and placenta (Belkacemi et al, 2005;Hirnet et al, 2003;Kim et al, 2006;Suzuki et al, 2008;Lee and Jeung, 2007).…”
Section: Introductionmentioning
confidence: 99%