THE CA2-MOBILIZING ACTIONS OF A JURKAT CELL EXTRACT ON MAMMALIAN-CELLS XENOPUS-LAEVIS OOCYTES()

Citation
P. Gilon et al., THE CA2-MOBILIZING ACTIONS OF A JURKAT CELL EXTRACT ON MAMMALIAN-CELLS XENOPUS-LAEVIS OOCYTES(), The Journal of biological chemistry, 270(14), 1995, pp. 8050-8055
Citations number
19
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
270
Issue
14
Year of publication
1995
Pages
8050 - 8055
Database
ISI
SICI code
0021-9258(1995)270:14<8050:TCAOAJ>2.0.ZU;2-E
Abstract
Randriamampita and Tsien (Randriamampita, C., and Tsien, R. Y, (1993) Nature 364, 809-814) suggested that an acid-extracted fraction from a Jurkat cell line contains a messenger responsible for the coupling of calcium entry to the depletion of intracellular stores, i.e. capacitat ive calcium entry, We found that the extract, prepared as described by Randriamampita and Tsien, caused Ca2+ entry in 1321N1 astrocytoma cel ls which was not blocked by the D-myo-1,4,5-trisphosphate-receptor ant agonist, heparin. In contrast to astrocytoma cells, when applied to mo use lacrimal acinar cells and rat hepatocytes the Jurkat extract alway s caused the release of intracellular Ca2+, followed by Ca2+ entry acr oss the plasma membrane, This activity of the extract on lacrimal cell s was blocked by either intracellular injection of heparin or extracel lular atropine, Similarly prepared lacrimal cell extracts gave Ca2+ re sponses when applied to astrocytoma cells or lacrimal cells which were similar to Obese for Jurkat-derived extract, However, extracts from h epatocytes had no effect, In most Xenopus oocytes, the Jurkat extract had no effect, while in a few oocytes, the extract gave a [Ca2+](i) re sponse similar to that seen in lacrimal cells, that is, release of Ca2 + followed by Ca2+ entry. We conclude that the actions of the Jurkat c ell extract are not consistent with its containing the long sought mes senger for capacitative calcium entry, It is Likely that this fraction contains a number of factors that mediate Ca2+ response in different cell types, possibly through receptor-mediated mechanisms.