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Migratory response of human natural killer cells to lymphotactin.

作者信息

Giancarlo B, Silvano S, Albert Z, Mantovani A, Allavena P

机构信息

Department of Immunology and Cell Biology, Mario Negri Institute, Milano, Italy.

出版信息

Eur J Immunol. 1996 Dec;26(12):3238-41. doi: 10.1002/eji.1830261260.

DOI:10.1002/eji.1830261260
PMID:8977329
Abstract

Lymphotactin (Lptn) is a new protein belonging to the C or gamma subfamily of chemokines with only two of the four cysteine residues. Lptn was reported to act specifically on T lymphocytes and not on monocytes and neutrophils. To understand better the spectrum of action of Lptn we have examined its ability to induce natural killer (NK) cell migration. Freshly isolated human NK cells as well as long-term cultured NK cells propagated in interleukin-2 (IL-2)-containing medium migrated in response to Lptn. Optimal activity was observed at concentrations ranging from 50 to 200 ng/ml, and the efficacy was comparable to that of MCP-1, the prototype of C-C chemokines. Migration in response to Lptn was chemotaxis rather than chemokinesis as determined in a checkerboard analysis. Migration of NK cells was comparable to that observed with T lymphocytes from the same donor, under the same experimental conditions. Finally, in contrast to other cytokines (IL-2 and IL-12) which in addition to chemotaxis augment NK cell adhesion to endothelial cells in vitro, Lptn did not affect the adhesiveness of NK cells to vascular endothelium.

摘要

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