A separate role for ICAM-1 and fluid shear in regulating leukocyte interactions with straight regions of venular wall and venular convergences

ICAM-1 和流体剪切在调节白细胞与小静脉壁和小静脉汇聚处直线区域的相互作用中起着独立作用

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作者:Ronen Sumagin, Kathleen A Lamkin-Kennard, Ingrid H Sarelius

Conclusions

In straight regions of different-sized venules, the variability in ICAM-1 expression accounts for the differences in leukocyte behavior; in converging regions, fluid shear potentially has a greater effect on leukocyte endothelial cell interactions.

Methods

Leukocyte behavior was quantified in blood-perfused microvascular networks in anesthetized mouse cremaster muscle, using intravital confocal microscopy. ICAM-1 expression and fluid shear rate were quantified by using ICAM-1 fluorescent labeling, fluorescent particle tracking, and computational fluid dynamics.

Objective

Variation in expression of adhesion molecules plays a key role in regulating leukocyte behavior, but the contribution of fluid shear to these interactions cannot be ignored. Here, we dissected the effects of each of these factors on leukocyte behavior in different venular regions. Materials and

Results

Tumor necrosis factor alpha induced an increase in ICAM-1 expression and abolished the differences observed among control venules of different sizes. Consequently, leukocyte adhesion was increased to a similar level across all vessel sizes [5.1+/-0.46 leukocytes/100 microm vs. 2.1+/-0.47 (control)], but remained significantly higher in venular convergences (7.8+/-0.4). Leukocyte transmigration occurred primarily in the smallest venules and venular convergences (23.9+/-5.1 and 31.9+/-2.7 leukocytes/10,000 microm(2) tissue, respectively). In venular convergences, the two inlet vessels are predicted to create a region of low velocity, increasing leukocyte adhesion probability. Conclusions: In straight regions of different-sized venules, the variability in ICAM-1 expression accounts for the differences in leukocyte behavior; in converging regions, fluid shear potentially has a greater effect on leukocyte endothelial cell interactions.

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