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Publication : α1β1 integrin-mediated adhesion inhibits macrophage exit from a peripheral inflammatory lesion.

First Author  Becker HM Year  2013
Journal  J Immunol Volume  190
Issue  8 Pages  4305-14
PubMed ID  23509351 Mgi Jnum  J:195298
Mgi Id  MGI:5477868 Doi  10.4049/jimmunol.1202097
Citation  Becker HM, et al. (2013) alpha1beta1 Integrin-Mediated Adhesion Inhibits Macrophage Exit from a Peripheral Inflammatory Lesion. J Immunol 190(8):4305-14
abstractText  Integrins are adhesion molecules critical for the recruitment of leukocytes from blood into peripheral tissues. However, whether integrins are also involved in leukocyte exit from peripheral tissues via afferent lymphatics to the draining lymph node remains poorly understood. In this article, we show that adhesion by the collagen IV-binding integrin alpha1beta1 unexpectedly inhibited macrophage exit from inflamed skin. We monitored macrophages exiting mouse footpads using a newly developed in situ pulse labeling technique. Blockade of alpha1beta1 integrin or genetic deletion (Itga1(-/-)) increased macrophage exit efficiency. Chemotaxis assays through collagen IV showed more efficient migration of Itga1(-/-) macrophages relative to wild type. Given that macrophages are key orchestrators of inflammation, alpha1beta1 integrin adhesion may represent a mechanism for regulating inflammatory responses by controlling macrophage exit or persistence in inflamed tissues.
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