TY  - JOUR
A1  - Hanisch, Uwe-Karsten
A1  - Van Rossum, Denise
A1  - Xie, Yiheng
A1  - Misselwitz, Rolf
A1  - Auriola, Seppo
A1  - Goldstein, Gundars
A1  - Koistinaho, Jari
A1  - Kettemann, Helmut
A1  - Möller, Thomas
A1  - Gast, Klaus
T1  - The microglia-activating potential of thrombin : the protease is not involved in the induction of proinflammatory cytokines and chemokines
N2  - The serine protease thrombin is known as a blood coagulation factor. Through limited cleavage of proteinase- activated receptors it can also control growth and functions in various cell types, including neurons, astrocytes, and microglia ( brain macrophages). A number of previous studies indicated that thrombin induces the release of proinflammatory cytokines and chemokines from microglial cells, suggesting another important role for the protease beyond hemostasis. In the present report, we provide evidence that this effect is not mediated by any proteolytic or non- proteolytic mechanism involving thrombin proper. Inhibition of the enzymatic thrombin activity did not affect the microglial release response. Instead the cyto-/chemokine-inducing activity solely resided in a high molecular weight protein fraction that could be isolated in trace amounts even from apparently homogenous alpha- and gamma-thrombin preparations. High molecular weight material contained thrombin-derived peptides as revealed by mass spectrometry but was devoid of thrombin-like enzymatic activity. Separated from the high molecular weight fraction by fast protein liquid chromatography, enzymatically intact alpha- and gamma-thrombin failed to trigger any release. Our findings may force a revision of the notion that thrombin itself is a direct proinflammatory release signal for microglia. In addition, they could be relevant for the study of other cellular activities and their assignment to this protease
Y1  - 2004
ER  -