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DOI: 10.1055/s-0038-1661231
Phosphorus Labeling of Proteins and Phospholipids in Intact Platelets in Response to pH 5.3
Publikationsverlauf
Received 02. Mai 1984
Accepted 22. Oktober 1984
Publikationsdatum:
18. Juli 2018 (online)
Summary
Previous studies had shown that when gel-filtered or washed human platelets were incubated at pH 5.3, the cells secreted their granule-stored materials suggesting that low pH can act as a platelet activator. We determined here whether the effects of low pH on platelet protein phosphorylation and on platelet lipid metabolism were consistent with this view. When washed human platelets were incubated for 20 min at pH 5.3 and electrophoresed on SDS-PAGE, there was a great increase in 32P-label in the 20,000 and 47,000 dalton protein bands. There was also an increase in the labeling of phosphatidic acid and a small decrease in phosphatidyl inositol. When the platelets were returned to pH 7.6, the 32P labeling of the 20,000 and 47,000 dalton bands was greatly reduced, and that of phosphatidic acid reduced to the control value, while the labeling of phosphatidyl inositol was increased above control. Incubation at pH 5.3 for 60 min gave the same pattern, but return to pH 7.6 resulted in only partial reversal of labeling of the two protein bands and little decrease in the label associated with phosphatidic acid, but the radioactivity in phosphatidyl inositol was greatly increased. The changes in the 32P-labeling of phospholipids and proteins after incubation of platelets at pH 5.3 may reflect an increase in cytoplasmic Ca++ resulting from leakage of Ca++ from intracellular storage sites, a process which becomes irreversible after longer time exposure to the low pH. The activation of human platelets at pH 5.3 is a slow process which may not be directly comparable to the fast events in the normal stimulation-response coupling, but which is accompanied by changes common to platelet activation. Most interesting in this respect is that a return to physiological conditions will reverse these events, although prolonged exposure will make them irreversible. These studies may therefore present a way to study the boundary between reversible and irreversible processes in platelets.
