Key result
Monocyte trafficking advances reveal distinct subsets and identify the spleen as an inflammatory monocyte reservoir.
Why the study?
Monocytes have diverse trafficking and migration behaviors critical to immune functions and inflammatory diseases, but recent advances in understanding these mechanisms needed synthesis.
Understanding monocyte trafficking and migration mechanisms is critical for elucidating their roles in cardiovascular diseases like atherosclerosis and for developing targeted therapeutics.
May guide targeted anti-inflammatory therapies in atherosclerosis; leaves open validation of splenic monocyte recruitment in clinical cohorts.
PURPOSE OF REVIEW: Monocytes play multiple roles in immune system functions and inflammatory diseases such as atherosclerosis. These roles are coupled to diverse trafficking and cellular migration behaviors. Here, we review recent advances in our understanding of such behaviors with emphasis on broad scale trafficking patterns and the cellular and molecular mechanisms regulating diapedesis, a central aspect of trafficking. RECENT FINDINGS: Monocytes consist of 'inflammatory' and 'resident' subsets, which exhibit differential functions and trafficking properties. Notably, the spleen has recently been identified as a reservoir of inflammatory monocytes, which are readily recruited to injured myocardium and possibly other tissues. Resident monocytes have been shown to undergo long-range crawling within the lumen of the microvasculature, which facilitates immune surveillance and rapid response to infection. Monocyte diapedesis has been demonstrated to utilize both para and transcellular migration routes facilitated by endothelial 'transmigratory cups'. A significant number of new adhesion molecules and signaling pathways have recently been uncovered as functional mediators and modulators of these processes. SUMMARY: Our improving understanding of monocyte trafficking and migration mechanisms has begun to shed light on the functions of these often enigmatic cells. Continued progress in this area will be critical for elucidating roles of monocytes in disease and for developing therapeutics that target monocytes.
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Kamei et al. (2009) conducted a review in Inflammatory diseases and atherosclerosis. Recent advances in monocyte trafficking reveal distinct inflammatory and resident subsets, with the spleen acting as a reservoir for inflammatory monocytes recruited to injured tissues.
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