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JCI table of contents: Nov. 21, 2007
Date:11/21/2007

Lo
National Institutes of Health, Bethesda, Maryland, USA.
Phone: (301) 451-8041, Fax: (301) 480-4581, Email: loc@nhlbi.nih.gov.

View the PDF of this article at: https://www.the-jci.org/article.php?id=33284


HEMATOLOGY: New role for intestinal protein in blood clotting

An intestinal protein known as BSDL that helps the body breakdown and absorb cholesterol is also found circulating in our bloodstream, where its role has been an enigma. However, in a new study, Laurence Panicot-Dubois and his colleagues at the Universit de la Mditerrane, France, have identified a role for blood-borne BSDL in blood clot formation.

In vitro analysis showed that BSDL enhances the activation of human platelets cells found in the blood that when activated are key to the formation of blood clots. In addition, in normal mice BSDL accumulated at sites of blood clot formation and in BSDL-deficient mice tail injury resulted in increased bleeding time. Further analysis revealed that BSDL mediated its effects on platelets in vitro and in vivo by binding a protein on the surface of platelets known as CXCR4. Indeed, inhibition of CXCR4 prevented BSDL-mediated human platelet activation, and eliminated BSDL accumulation and reduced blot clot size in mice. These data led the authors to conclude that the interaction between BSDL and CXCR4 might be a new target for therapies to treat conditions in which blood clots form inappropriately inside blood vessels, such as occurs in individuals with pancreatic cancer.

TITLE: Bile saltdependent lipase interacts with platelet CXCR4 and modulates thrombus formation in mice and humans

AUTHOR CONTACT:

Laurence Panicot-Dubois
Universit de la Mditerrane, Facult de Mdecine Timone, Marseille, France
Phone: 33-491-324-400; Fax: 33-491-830-187; E-mail: '/>"/>

Contact: Karen Honey
press_releases@the-jci.org
215-573-1850
Journal of Clinical Investigation
Source:Eurekalert

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