Animal experiments

AS Ariane Schumski
AO Almudena Ortega-Gómez
KW Kanin Wichapong
CW Carla Winter
PL Patricia Lemnitzer
JV Joana R. Viola
MP Mayra Pinilla-Vera
EF Eduardo Folco
VS Victor Solis-Mezarino
MV Moritz Völker-Albert
SM Sanne L. Maas
CP Chang Pan
LO Laura Perez Olivares
JW Janine Winter
TH Tilman Hackeng
MK Mikael C.I. Karlsson
TZ Tanja Zeller
AI Axel Imhof
RB Rebecca M Baron
GN Gerry A.F. Nicolaes
PL Peter Libby
LM Lars Maegdefessel
FK Frits Kamp
MB Martin Benoit
YD Yvonne Döring
OS Oliver Soehnlein
request Request a Protocol
ask Ask a question
Favorite

We surveyed atheroprogression in Apoe−/− or Apoe−/−Cx3cr1GFP reporter mice on C57Bl/6J background after 4 weeks of high-fat diet (HFD) (21% fat, Ssniff). Endotoxinemia was induced by intraperitoneal (i.p.) injection of lipopolysaccharide (LPS, Escherichia coli, O111:B4, Sigma Aldrich, 1 mg/kg BW, i.p.). Control mice received vehicle (PBS, 100 μl, i.p.). Thereafter, atherosclerotic lesions were analyzed in aortic root sections or cell adhesion was studied by intravital microscopy of the left carotid artery. To assess the effect of NETs we blocked NET-formation with BB Cl-amidine (1 mg/kg BW, Cayman Chemical Company). In additional experiments, mice received antibodies to histone H2a (20 μg/mouse, Biorbyt), its respective IgG isotype control (Jackson ImmunoResearch), or a cyclical histone 2A interference peptide (CHIP, 5 mg/kg BW). All animal experiments were approved by the local ethics committee and performed in accordance with institutional guidelines.

Do you have any questions about this protocol?

Post your question to gather feedback from the community. We will also invite the authors of this article to respond.

post Post a Question
0 Q&A