Sphingosine-1-phosphate (Sph-1-P) is the initial product of catabolism of sphingosine by sphingosine kinase and is cleaved by Sph-1-P lyase to a fatty aldehyde and ethanolamine phosphate. This phosphorylated sphingoid base is not only an intermediary catabolite, but also a bioactive lipid with important functions, including stimulation of cell proliferation in Swiss 3T3 fibroblasts and inhibition of tumor cell motility. In the present study, we examined functional roles of Sph-1-P in human platelets. Sph-1-P induced platelet shape change and aggregation reactions, although it failed to elicit secretion. Sphingosine, ceramide, sphingomyelin, and N,N-dimethylsphingosine did not mimic the positive effects of Sph-1-P on platelets. Subthreshold concentrations of Sph-1-P and weak platelet agonists such as adenosine diphosphate (ADP) and epinephrine synergistically elicited aggregation, which may be important for efficient amplification of platelet activation. Sph-1-P induced intracellular Ca2+ mobilization and the dose-response for Ca2+ release correlated closely with the concentration required for induction of shape change. On addition of [3H]sphingosine to intact platelets, the label was rapidly converted to Sph-1-P, and subsequently to ceramide and sphingomyelin. Interestingly, the Sph-1-P formed was specifically released into medium on stimulation of platelets with physiologic agonists. The amount of Sph-1-P in platelets, as measured by its conversion into radiolabeled N-acetyl-Sph- 1-P, was 1.4 nmol/10(9) cells and was about four times higher than the mass of Sph present. When compared by mole percent Sph-1- P/phospholipid, the value for platelets is over 10 times higher than that for neutrophils. Our results suggest that Sph-1-P, rapidly converted from sphingosine, abundantly stored in platelets, and released on the cell activation, may play a physiologic role in thrombosis, hemostasis, and the natural wound-healing processes.
Skip Nav Destination
ARTICLES|
July 1, 1995
Sphingosine-1-phosphate: a platelet-activating sphingolipid released from agonist-stimulated human platelets
Y Yatomi,
Y Yatomi
Biomembrane Institute, University of Washington, Seattle 98119, USA.
Search for other works by this author on:
F Ruan,
F Ruan
Biomembrane Institute, University of Washington, Seattle 98119, USA.
Search for other works by this author on:
S Hakomori,
S Hakomori
Biomembrane Institute, University of Washington, Seattle 98119, USA.
Search for other works by this author on:
Y Igarashi
Y Igarashi
Biomembrane Institute, University of Washington, Seattle 98119, USA.
Search for other works by this author on:
Blood (1995) 86 (1): 193–202.
Citation
Y Yatomi, F Ruan, S Hakomori, Y Igarashi; Sphingosine-1-phosphate: a platelet-activating sphingolipid released from agonist-stimulated human platelets. Blood 1995; 86 (1): 193–202. doi: https://doi.org/10.1182/blood.V86.1.193.bloodjournal861193
Download citation file:
July 1 1995
Advertisement intended for health care professionals
Cited By
Advertisement intended for health care professionals
This feature is available to Subscribers Only
Sign In or Create an Account Close Modal