The adhesion molecule L1, which is extensively characterized in the nervous system, is also expressed in dendritic cells(DCs), but its function there has remained elusive. To address this issue, we ablated L1 expression in DCs of conditional knockout mice. L1-deficient DCs were impaired in adhesion to and transmigration through monolayers of either lymphatic or blood vessel endothelial cells, implicating L1 in transendothelial migration of DCs. In agreement with these findings, L1 was expressed in cutaneous DCs that migrated to draining lymph nodes, and its ablation reduced DC trafficking in vivo. Within the skin, L1 was found in Langerhans cells but not in dermal DCs, and L1 deficiency impaired Langerhans cell migration. Under inflammatory conditions, L1 also became expressed in vascular endothe- lium and enhanced transmigration of DCs, likely through L1 homophilic interactions. Our results implicate L1 in the regulation of DC trafficking and shed light on novel mechanisms underlying transendothelial migration of DCs. These observations might offer novel therapeutic perspectives for the treatment of certain immunological disorders.

The adhesion molecule L1 regulates transendothelial migration and trafficking of dendritic cells / L. Maddaluno, S.E. Verbrugge, C. Martinoli, G. Matteoli, A. Chiavelli, Y. Zeng, E.D. Williams, M. Rescigno, U. Cavallaro. - In: JOURNAL OF EXPERIMENTAL MEDICINE. - ISSN 0022-1007. - 206:3(2009 Mar 16), pp. 623-635.

The adhesion molecule L1 regulates transendothelial migration and trafficking of dendritic cells

L. Maddaluno
Primo
;
A. Chiavelli;M. Rescigno
Penultimo
;
2009-03-16

Abstract

The adhesion molecule L1, which is extensively characterized in the nervous system, is also expressed in dendritic cells(DCs), but its function there has remained elusive. To address this issue, we ablated L1 expression in DCs of conditional knockout mice. L1-deficient DCs were impaired in adhesion to and transmigration through monolayers of either lymphatic or blood vessel endothelial cells, implicating L1 in transendothelial migration of DCs. In agreement with these findings, L1 was expressed in cutaneous DCs that migrated to draining lymph nodes, and its ablation reduced DC trafficking in vivo. Within the skin, L1 was found in Langerhans cells but not in dermal DCs, and L1 deficiency impaired Langerhans cell migration. Under inflammatory conditions, L1 also became expressed in vascular endothe- lium and enhanced transmigration of DCs, likely through L1 homophilic interactions. Our results implicate L1 in the regulation of DC trafficking and shed light on novel mechanisms underlying transendothelial migration of DCs. These observations might offer novel therapeutic perspectives for the treatment of certain immunological disorders.
animals; blood vessels; cell adhesion; cell communication; dendritic cells; dermatitis, contact; endothelial cells; endothelium; female; humans; langerhans cells; lymph nodes; male; mice; mice, knockout; neural cell adhesion molecule l1; tumor necrosis factor-alpha; cell movement; immunology; immunology and allergy; medicine (all)
Settore MED/04 - Patologia Generale
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/425560
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