(Circulation. 2007;115:e187.)
© 2007 American Heart Association, Inc.
Correspondence |
Millennium Pharmaceuticals, Inc, Cambridge, Mass
Cardiovascular Division, Brigham and Womens Hospital, Harvard Medical School, Boston, Mass
Division of Cardiovascular Medicine, Case Cardiovascular Center, University HospitalsCase Medical Center, Case Western Reserve University School of Medicine, Cleveland, Ohio
Cardiology Division, Massachusetts General Hospital, Harvard Medical School, Boston, Mass
We would like to thank Dr Krishnan and colleagues for their interest in our work. They have raised additional limitations of our work and question whether platelets express myeloid-related protein-14 (MRP-14). Their caution is reasonable. However, we have provided additional evidence that MRP-14 is expressed in bone marrowderived human megakaryocytes and megakaryocytes differentiated in vitro from CD34-positive peripheral blood cells (Data Supplement Figure I of our article1). We also have detected MRP-8/14 protein in human platelets by flow cytometry (data not shown). Double antibody experiments show costaining for the platelet-specific marker glycoprotein IIb/IIIa and for MRP-8/14. MRP-8/14positive platelets were negative for the leukocyte marker CD45, ruling out leukocyte contamination as a source of the MRP-8/14 signal.
| Acknowledgments |
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This study was funded in part by Millennium Pharmaceuticals. Drs Healy, Damokosh, and Lillie and M.D. Pickard, T.L. Dowie, and L. Poisson are employees of Millennium Pharmaceuticals and played roles in the design of the study, data collection, data analysis, data interpretation, and the writing of the report. Drs Simon and Libby report having served as consultants and advisors to Millennium Pharmaceuticals. Dr Ridker is named as a coinventor on patents filed by Brigham and Womens Hospital that relate to the use of inflammatory biological markers in cardiovascular disease. The other authors report no conflicts of interest.
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