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PMID: 2749601 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Heparin inhibition of endotoxin-dependent Limulus amebocyte lysate coagulation.

Thrombosis and haemostasis ·Vol. 61 ·No. 2 ·1989-04-25 ·Pages 294-7

Marcum JA, Levin J

Abstract

Addition of commercial heparin to preparations of the coagulation system obtained by hypotonic lysis of Limulus amebocytes, prior to the addition of endotoxin from gram-negative bacteria, inhibited gelation. Activation of the cell-lysate proclotting enzyme, utilizing a diluted lysate preparation and synthetic substrates, was inhibited to a comparable extent with either anticoagulantly active or inactive heparin. Other glycosaminoglycans, including heparan sulfate, dermatan sulfate, chondroitin 4-sulfate, and chondroitin 6-sulfate, did not inhibit the generation of clotting enzyme activity. Experiments conducted with preparations of proactivator(s) and proclotting enzyme, obtained by fractionation of lysate with heparin-Sepharose, revealed that inhibition of endotoxin-dependent activation of amebocyte lysate by heparin is mediated by precipitation of the proactivator(s) and can be prevented by increasing the salt concentration.

MeSH Terms
Animals Chemical Precipitation Endotoxins/pharmacology Heparin/pharmacology Limulus Test
Chemicals
Endotoxins Heparin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Marcum J A
Marine Biological Laboratory, Woods Hole, MA.
Levin J
Article Info
Journal
Thrombosis and haemostasis
Abbr.
Thromb Haemost
ISSN
0340-6245
Published
1989-04-25
Pages
294-7
Language
English
Region
Germany
NLM ID
7608063
Subset
IM
Grants
NHLBI NIH HHS · HL31035 · United States
NHLBI NIH HHS · HL34800 · United States
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