Polymorphonuclear leukocyte-myocyte interaction: an early event in collar-induced rabbit carotid intimal thickening
Elena Donetti1, Roberta Baetta, Carmen Comparato
1Department of Human Anatomy, University of Milan, Milan, Italy. elena.donetti@unimi.it
Abstract:
The importance of mononuclear leukocyte (MO) adhesion to dysfunctional endothelium and migration to the subendothelial space in the early phases of atherogenesis is well established. Few studies have addressed the relevance of polymorphonuclear leukocytes (PMNs) in the context of evolving lesions, and nothing is known about PMN interaction with vascular smooth muscle cells (SMCs). In this study, we investigated leukocyte/SMC interactions in a model of rabbit carotid injury induced by placement of a silastic collar. This procedure leads to the development of intimal thickening characterized by SMC accumulation preceded by an abundant leukocyte infiltration. By transmission electron microscopy and immunocytochemistry, we demonstrated the occurrence of PMN infiltration starting at 6 h and ceasing within 72 h after collar placement. A previously unknown extensive interaction between medial myocytes and PMNs was detected, referring to emperipolesis, an active phenomenon of cells engulfing other cells in a process other than phagocytosis. PMNs, but not MOs, were internalized by SMCs, which showed ultrastructural features intermediate between the true contractile and the fully synthetic phenotype without exhibiting any sign of injury. Emperipolesis preceded any detectable cell proliferation in the vessel wall and disappeared within 72 h, following the kinetic of PMN infiltration in the vessel wall. In summary, our findings show the occurrence of an active and selective interaction between PMNs and SMCs via emperipolesis during the early phases of intimal thickening after perivascular collaring. However, the overall etiology of the phenomena described in the present study and their pathophysiological significance should be further investigated.
Insights
Polymorphonuclear leukocytes (PMNs) actively interact with vascular smooth muscle cells (SMCs) during early atherogenesis. This previously unknown emperipolesis phenomenon involves SMCs internalizing PMNs, preceding lesion development.
Area of Science:
- Vascular Biology
- Cellular Interactions
- Atherosclerosis Research
Background:
- Mononuclear leukocyte (MO) adhesion and migration are key in early atherogenesis.
- The role of polymorphonuclear leukocytes (PMNs) in evolving lesions and their interaction with vascular smooth muscle cells (SMCs) remains unclear.
Purpose of the Study:
- To investigate leukocyte/SMC interactions in a rabbit carotid artery injury model.
- To elucidate the role of PMNs in the early stages of intimal thickening.
Main Methods:
- Rabbit carotid artery injury induced by a silastic collar.
- Transmission electron microscopy and immunocytochemistry to analyze cellular interactions.
- Kinetics of PMN infiltration and SMC changes observed.
Main Results:
- PMN infiltration occurred between 6 and 72 hours post-injury.
- A novel interaction, emperipolesis, was observed where SMCs internalized PMNs.
- PMN internalization by SMCs preceded detectable cell proliferation and showed no signs of injury.
Conclusions:
- PMNs and SMCs engage in active, selective emperipolesis during early intimal thickening.
- This interaction is a novel finding in the context of vascular injury and atherogenesis.
- Further research is needed to understand the etiology and pathophysiological significance of this phenomenon.
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