Disciplines
Clinical Medicine (70%); Medical-Theoretical Sciences, Pharmacy (30%)
Keywords
ILEI/FAM3C,
Myocardial Infarct,
Myocardiocyte Protection,
Catecholamine Release,
Chromaffin Cells Of The Adrenal Medulla,
Neuroendocrine Regulation
Abstract
Heart attack is a leading cause of death worldwide. Despite the significant improvement in
mortality, acute myocardial infarction and as consequence the development of heart failure is
a significant clinically unresolved issue. Novel approaches to allivate myocardial injury and
infarction and heart failure due to heart attack are urgently needed. The secreted protein
FAM3C/ILEI has been identified as protective factor for the heart if supplied in excess, which
raises the question if it can be harnessed for therapy. The funded research explores the novel
idea that an endogenous ILEI protein pool could serve and be mobilized as emergency reservoir
of the ILEI protein to protect the heart against infarction-insult and mitigate the sign of heart
failure.
Agnes Csiszars team at the Center for Cancer Research in cooperation with researchers around
Attila Kiss at the Center of Biomedical Research and Translational Surgery, Medical
University of Vienna will utilize genetically modified mice with tissue-specific FAM3C/ILEI
deletion combined with a mouse model of myocardial infarction extended with in vitro models
and human patient material to test the hypothesis of an endogenous ILEI-mediated heart
protection as well as set the path to the development of new therapeutic strategies that boost
this natural defense mechanism.
Beside the strong translational approach this project will also foster the mechanistic
understanding on the function of endogenous ILEI protein pools and their association to
myocardial infarction.