Planta Med 2004; 70(2): 127-131
DOI: 10.1055/s-2004-815488
Original Paper
Biochemistry
© Georg Thieme Verlag Stuttgart · New York

Secondary Metabolites from Marine Cyanobacteria and Algae Inhibit LFA-1/ICAM-1 Mediated Cell Adhesion

Satoshi Takamatsu1 , Dale G. Nagle2 , William H. Gerwick3
  • 1National Center for Natural Products Research
  • 2Department of Pharmacognosy, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS 38677-1848
  • 3College of Pharmacy, Oregon State University, Corvallis, Oregon 97331
Further Information

Publication History

Received: July 7, 2003

Accepted: October 3, 2003

Publication Date:
02 March 2004 (online)

Abstract

An assay for inhibitors of LFA-1/ICAM-1 mediated cell-cell adhesion has been employed to identify new pharmacologically active compounds from marine cyanobacteria and algae. From a panel of sixty unusual marine natural products, seventeen compounds inhibited LFA-1/ICAM-1-based cell aggregation without showing significant cytotoxicity in the primary assay. Six compounds inhibited the cell-cell adhesion of HL-60 cells to CHO-ICAM-1 cells. The unusual oxylipin Cymathere aldehyde methyl ester (IC50 3.5 μM), cyanobacterial lipopeptides microcolins B (IC50 0.15 μM) and D (IC50 0.9 μM), bromophenol avrainvilleol (IC50 2.2 μM), sesquiterpene cymopol (IC50 2.7 μM), and cryptophyte derived compound styrylchromone hormothamnione diacetate (IC50 1.5 μM) significantly inhibited LFA-1/ICAM-1 mediated cell adhesion. The pharmacological activity and structure-activity relationships of selected marine algal metabolites are described.

Abbreviations

LFA-1:Lymphocyte function-associated molecule-1

ICAM-1:Intercellular cell adhesion molecule-1

PMA:Phorbol 12-myristate 13-acetate

HL-60:Promyelocytic human leukemia-60

CHO:Chinese hamster ovary

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Satoshi Takamatsu

Phone: 662-915-1139

Fax: 662-915-7062

Email: stakamat@olemiss.edu

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