Jenner S, Farndale R W, Sage S O
Physiological Laboratory, University of Cambridge, U.K.
Biochem J. 1994 Oct 15;303 ( Pt 2)(Pt 2):337-9. doi: 10.1042/bj3030337.
To investigate the possible involvement of tyrosine phosphorylation in the process of store-regulated Ca2+ entry, ionomycin (in the presence of EGTA) was used to deplete the intracellular Ca2+ stores of fura-2-loaded human platelets, and the effect of refilling with Ca2+, Ba2+ or Sr2+ evaluated. Depletion of the intracellular Ca2+ stores resulted in an increase in protein tyrosine phosporylation. This increase is reversed when the stores were refilled in Ca2+ or Sr2+, but not Ba2+. Refilling of the stores with Ca2+ or Sr2+, but not Ba2+, suppressed Mn2+ entry. These findings support the hypothesis that tyrosine phosphorylation plays a role in mediating store-regulated Ca2+ entry in human platelets and provides evidence for tyrosine phosphatase activity regulated by the Ca2+ content of the intracellular stores.
为了研究酪氨酸磷酸化在储存调控的Ca2+内流过程中可能的作用,使用离子霉素(在乙二醇双四乙酸存在下)耗尽负载fura-2的人血小板的细胞内Ca2+储存,并评估用Ca2+、Ba2+或Sr2+重新填充的效果。细胞内Ca2+储存的耗尽导致蛋白质酪氨酸磷酸化增加。当储存用Ca2+或Sr2+重新填充时,这种增加被逆转,但用Ba2+重新填充则不会。用Ca2+或Sr2+而不是Ba2+重新填充储存会抑制Mn2+内流。这些发现支持了酪氨酸磷酸化在介导人血小板中储存调控的Ca2+内流中起作用的假设,并为受细胞内储存Ca2+含量调节的酪氨酸磷酸酶活性提供了证据。