Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 11 May 1979:
Vol. 204. no. 4393, pp. 631 - 633
DOI: 10.1126/science.86210

Articles

Science, Vol 204, Issue 4393, 631-633
Copyright © 1979 by American Association for the Advancement of Science


articles

Inhibition of mast cell histamine secretion by N-substituteed derivatives of phosphatidylserine

TW Martin and D Lagunoff

The structural basis for the highly specific action of phosphatidylserine in enhancing mast cell histamine secretion induced by concanavalin A was investigated by studying the activities of three N-substituted derivatives: N-acetyl phosphatidylserine, N-1-dimethylaminonaphthalene-5-sulfonly phosphatidylserine, and N-4-nitrobenzo-2-oxa-1,3-diazole phosphatidylserine. None of the derivatives was capable of activating concanavalin A-induced histamine secretion at concentrations two to three times that required for maximal activation by phosphatidylserine. Instead, the derivatives were found to inhibit the secretory response of mast cells to the calcium ionophore A23187 as well as to concanavalin A. The inhibition was noncytotoxic, partially reversible by washing, and associated with binding of N-substituted phosphatidylserine to the mast cell.





To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)