Lysophosphatidic acid (LPA) plays various roles in the regulation of cell growth as a lipid mediator. We studied the effect of LPA on intracellular Ca 2ุ concentration ([Ca 2ุ ] i ) with Fura-2 in the neural retina of chick embryo during neurogenesis. Bath application of LPA (1-100 M) to the embryon
Capacitative Ca2+ influx in the neural retina of chick embryo
โ Scribed by Sakaki, Yoko ;Sugioka, Miho ;Fukuda, Yutaka ;Yamashita, Masayuki
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 245 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0022-3034
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โฆ Synopsis
Depletion of intracellular Ca 2/ gradually until E13, when the Ca 2/ rise almost disapstores induces a capacitative Ca 2/ influx in non-neural peared. This developmental profile correlated with the cells. It has been unknown whether the capacitative Ca 2/ influx occurs in the cells of nervous systems. We decline in the mitotic activities of the retinal cells studfound the capacitative Ca 2/ influx in the neural retina ied by Prada et al. The fluorescence imaging with the of early embryonic chick with Fura-2 fluorescence
vertical slice of the E9 retina showed that the site at measurements. A Ca 2/ -free medium containing thapwhich the thapsigargin-induced Ca 2/ rise was largest sigargin (500 nM), an inhibitor of Ca 2/ -ATPase of was the most outer layer of the retina, where proliferintracellular Ca 2/ stores, was applied to the neural ating cells are located. This spatial distribution and retina of embryonic day 3 (E3) chick. A rise in intrathe above developmental profile may suggest that the cellular Ca 2/ concentration was evoked after the reincapacitative Ca 2/ influx occurs at the early period of troduction of extracellular Ca 2/ , and this Ca 2/ rise neurogenesis when the cells have mitotic activities. was suppressed by Zn 2/ (1 mM) and Ni 2/ (5 mM).
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