Ingramon, a Peptide Inhibitor of MCP-1 Chemokine, Reduces Migration of Blood Monocytes Stimulated by Glioma-Conditioned Medium


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Abstract

Malignant gliomas are most common and fatal primary brain tumors. In addition to neoplastic cells, the tumor tissue contains microglial cells and monocyte-derived macrophages. It is an established fact that monocyte recruiting promotes the tumor growth and dissemination. Monocyte chemotactic protein-1 (MCP-1) is the major attractant for monocytes. We have previously synthesized an MCP-1 antagonist ingramon, a synthetic peptide fragment (65–76) of this chemokine. In the present study, we demonstrated that glioma-conditioned medium contains MCP-1 and stimulates migration of blood monocytes. Ingramon inhibited the effect of glioma-conditioned medium on monocyte migration.

About the authors

T. L. Krasnikova

Russian Cardiology Research-and-Development Centre, |Ministry of Health of the Russian Federation

Author for correspondence.
Email: tlkrasnikova@gmail.com
Russian Federation, Moscow

T. I. Arefieva

Russian Cardiology Research-and-Development Centre, |Ministry of Health of the Russian Federation

Email: tlkrasnikova@gmail.com
Russian Federation, Moscow

E. A. Pylaeva

Russian Cardiology Research-and-Development Centre, |Ministry of Health of the Russian Federation

Email: tlkrasnikova@gmail.com
Russian Federation, Moscow

M. V. Sidorova

Russian Cardiology Research-and-Development Centre, |Ministry of Health of the Russian Federation

Email: tlkrasnikova@gmail.com
Russian Federation, Moscow


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