Sickle Red Cell-Endothelium Interactions

被引:131
作者
Kaul, Dhananjay K. [1 ]
Finnegan, Eileen [2 ]
Barabino, Gilda A. [2 ]
机构
[1] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[2] Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
基金
美国国家卫生研究院;
关键词
sickle red cell adhesion; red cell heterogeneity; vaso-occlusion; leukocytes; adhesion molecules; adhesion inhibition; VASCULAR ENDOTHELIUM; FETAL-HEMOGLOBIN; ERYTHROCYTE ADHERENCE; P-SELECTIN; ADHESIVE INTERACTIONS; PLATELET ACTIVATION; IN-VIVO; ANEMIA; DISEASE; FLOW;
D O I
10.1080/10739680802279394
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Periodic recurrence of painful vaso-occlusive crisis is the defining feature of sickle cell disease. Among multiple pathologies associated with this disease, sickle red cell-endothelium interaction has been implicated as a potential initiating mechanism in vaso-occlusive events. This review focuses on various interrelated mechanisms involved in human sickle red cell adhesion. We discuss in vitro and microcirculatory findings on sickle red cell adhesion, its potential role in vaso-occlusion, and the current understanding of receptor-ligand interactions involved in this pathological phenomenon. In addition, we discuss the contribution of other cellular interactions (leukocytes recruitment and leukocyte-red cell interaction) to vaso-occlusion, as observed in transgenic sickle mouse models. Emphasis is given to recently discovered adhesion molecules that play a predominant role in mediating human sickle red cell adhesion. Finally, we analyze various therapeutic approaches for inhibiting sickle red cell adhesion by targeting adhesion molecules and also consider therapeutic strategies that target stimuli involved in endothelial activation and initiation of adhesion.
引用
收藏
页码:97 / 111
页数:15
相关论文
共 85 条
[41]   CATION-TRANSPORT AND VOLUME REGULATION IN SICKLE RED-BLOOD-CELLS [J].
JOINER, CH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (02) :C251-C270
[42]   Peptides based on αV-binding domains of erythrocyte ICAM-4 inhibit sickle red cell-endothelial interactions and vaso-occlusion in the microcirculation [J].
Kaul, Dhananjay K. ;
Liu, Xiao-Du ;
Zhang, Xiaoqin ;
Mankelow, Tosti ;
Parsons, Stephen ;
Spring, Frances ;
An, Xiuli ;
Mohandas, Narla ;
Anstee, David ;
Chasis, Joel Anne .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 291 (05) :C922-C930
[43]   Robust vascular protective effect of hydroxamic acid derivatives in a sickle mouse model of inflammation [J].
Kaul, Dhananjay K. ;
Kollander, Rahn ;
Mahaseth, Hemchandra ;
Liu, Xiao-Du ;
Solovey, Anna ;
Belcher, John ;
Kelm, Robert J., Jr. ;
Vercellotti, Gregory M. ;
Hebbel, Robert P. .
MICROCIRCULATION, 2006, 13 (06) :489-497
[44]   Inhibition of sickle red cell adhesion and vasoocclusion in the microcirculation by antioxidants [J].
Kaul, Dhananjay K. ;
Liu, Xiao-du ;
Zhang, Xiaoqin ;
Ma, Li ;
Hsia, Carleton J. C. ;
Nagel, Ronald L. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2006, 291 (01) :H167-H175
[45]   Effect of fetal hemoglobin on microvascular regulation in sickle transgenic-knockout mice [J].
Kaul, DK ;
Liu, XD ;
Chang, HY ;
Nagel, RL ;
Fabry, ME .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (08) :1136-1145
[46]   Hypoxia/reoxygenation causes inflammatory response in transgenic sickle mice but not in normal mice [J].
Kaul, DK ;
Hebbel, RP .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (03) :411-420
[47]  
KAUL DK, 1989, ANN NY ACAD SCI, V565, P316, DOI 10.1111/j.1749-6632.1989.tb24179.x
[48]   Monoclonal antibodies to αVβ3 (7E3 and LM609) inhibit sickle red blood cell-endothelium interactions induced by platelet-activating factor [J].
Kaul, DK ;
Tsai, HM ;
Liu, XD ;
Nakada, MT ;
Nagel, RL ;
Coller, BS .
BLOOD, 2000, 95 (02) :368-374
[49]   In vivo studies of sickle red blood cells [J].
Kaul, DK ;
Fabry, ME .
MICROCIRCULATION, 2004, 11 (02) :153-165
[50]   MICROVASCULAR SITES AND CHARACTERISTICS OF SICKLE-CELL ADHESION TO VASCULAR ENDOTHELIUM IN SHEAR-FLOW CONDITIONS - PATHOPHYSIOLOGICAL IMPLICATIONS [J].
KAUL, DK ;
FABRY, ME ;
NAGEL, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (09) :3356-3360