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Differential Kv1.3, KCa3.1, and Kir2.1 expression in "classically" and "alternatively" activated microglia.

Glia (2016-10-04)
Hai M Nguyen, Eva M Grössinger, Makoto Horiuchi, Kyle W Davis, Lee-Way Jin, Izumi Maezawa, Heike Wulff
ABSTRACT

Microglia are highly plastic cells that can assume different phenotypes in response to microenvironmental signals. Lipopolysaccharide (LPS) and interferon-γ (IFN-γ) promote differentiation into classically activated M1-like microglia, which produce high levels of pro-inflammatory cytokines and nitric oxide and are thought to contribute to neurological damage in ischemic stroke and Alzheimer's disease. IL-4 in contrast induces a phenotype associated with anti-inflammatory effects and tissue repair. We here investigated whether these microglia subsets vary in their K

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Sigma-Aldrich
Triton X-100, laboratory grade
Sigma-Aldrich
TRAM-34, ≥98% (HPLC), solid
Sigma-Aldrich
Bovine IFNG / Interferon Gamma ELISA Kit, for serum, plasma and cell culture supernatants
Sigma-Aldrich
ML133 hydrochloride, ≥95% (HPLC)