Flow Cytometric Evaluation of the Ongoing Angiogenic Response in Rat Cardiac Tissue Following Myocardial Infarction
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Flow Cytometric Evaluation of the Ongoing Angiogenic Response in Rat Cardiac Tissue Following Myocardial Infarction. / Hoeeg, Cecilie; Ringgaard, Lars; Christensen, Esben; Follin, Bjarke; Bentsen, Simon; Ripa, Rasmus Sejersten; Kjaer, Andreas.
I: Current Protocols, Bind 1, Nr. 2, e40, 2021.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Flow Cytometric Evaluation of the Ongoing Angiogenic Response in Rat Cardiac Tissue Following Myocardial Infarction
AU - Hoeeg, Cecilie
AU - Ringgaard, Lars
AU - Christensen, Esben
AU - Follin, Bjarke
AU - Bentsen, Simon
AU - Ripa, Rasmus Sejersten
AU - Kjaer, Andreas
N1 - Publisher Copyright: © 2021 Wiley Periodicals LLC
PY - 2021
Y1 - 2021
N2 - Angiogenesis is involved in regeneration of cardiac tissue following acute myocardial infarction (MI), a disease often investigated in rat models. Therefore, the ability to thoroughly evaluate the angiogenic response following experimentally induced MI in rats, and distinguish it from inflammation, is desired. This would enable evaluation of the angiogenic potential of new therapeutics and improve knowledge on MI pathophysiology. Due to the complex response to MI involving multiple cell types and the limited selection of rat-specific antibodies, careful optimization is crucial to capture this complexity. Here, we present an 8-color flow cytometry-based multicolor panel that will enable quantification of the ongoing angiogenic response as well as characterize the cells involved. A detailed description of tissue preparation, immunostaining, and gating strategy is provided.
AB - Angiogenesis is involved in regeneration of cardiac tissue following acute myocardial infarction (MI), a disease often investigated in rat models. Therefore, the ability to thoroughly evaluate the angiogenic response following experimentally induced MI in rats, and distinguish it from inflammation, is desired. This would enable evaluation of the angiogenic potential of new therapeutics and improve knowledge on MI pathophysiology. Due to the complex response to MI involving multiple cell types and the limited selection of rat-specific antibodies, careful optimization is crucial to capture this complexity. Here, we present an 8-color flow cytometry-based multicolor panel that will enable quantification of the ongoing angiogenic response as well as characterize the cells involved. A detailed description of tissue preparation, immunostaining, and gating strategy is provided.
KW - angiogenesis
KW - flow cytometry
KW - immune response
KW - myocardial infarction
KW - rat cardiac tissue
KW - rat heart
U2 - 10.1002/cpz1.40
DO - 10.1002/cpz1.40
M3 - Journal article
C2 - 33570836
AN - SCOPUS:85102206402
VL - 1
JO - Current Protocols
JF - Current Protocols
SN - 2691-1299
IS - 2
M1 - e40
ER -
ID: 279627447