4.3 Article

Thrombin regulates CD40 expression in microglial cells

Journal

NEUROREPORT
Volume 19, Issue 7, Pages 757-760

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/WNR.0b013e3282fdf4e7

Keywords

CD40; microglia; multiple sclerosis; pharmaceutical-grade thrombin; proteinase-activated receptor; stroke

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Funding

  1. NINDS NIH HHS [K08 NS047309, R01 NS044337-04, NS44337, NS047309] Funding Source: Medline

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Microglial cells are the innate immune cells of the central nervous system and quickly respond to injury by proliferation, cytokine release, and increased cell surface antigen expression. Thrombin is a multifunctional serine proteinase, which has the capability to activate microglial cells. Here, we report that pharmaceutical-grade thrombin dose-dependently increases the expression of CD40 in N9 microglial cells. This effect is blocked by a thrombin inhibitor, mimicked by thrombin receptor-activating peptide and modified by mitogen-activated protein kinase pathway inhibitors. Thrombin-induced CD40 regulation might play a role in diseases with breakdown of the blood-brain barrier such as multiple sclerosis or stroke.

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