TY - JOUR
T1 - Non-invasive in vivo imaging of changes in Collagen III turnover in myocardial fibrosis
AU - Chaher, Nadia
AU - Lacerda, Sara
AU - Digilio, Giuseppe
AU - Padovan, Sergio
AU - Gao, Ling
AU - Lavin, Begona
AU - Stefania, Rachele
AU - Velasco Jimeno, Carlos
AU - Cruz, Gastão
AU - Prieto Vasquez, Claudia
AU - Botnar, Rene
AU - Phinikaridou, Alkystis
PY - 2024/9/17
Y1 - 2024/9/17
N2 - Heart failure (HF) affects 64 million people globally with enormous societal and healthcare costs. Myocardial fibrosis, characterised by changes in collagen content drives HF. Despite evidence that collagen type III (COL3) content changes during myocardial fibrosis, in vivo imaging of COL3 has not been achieved. Here, we discovered the first imaging probe that binds to COL3 with high affinity and specificity, by screening candidate peptide-based probes. Characterisation of the probe showed favourable magnetic and biodistribution properties. The probe’s potential for in vivo molecular cardiac magnetic resonance imaging was evaluated in a murine model of myocardial infarction. Using the new probe, we were able to map and quantify, previously undetectable, spatiotemporal changes in COL3 after myocardial infarction and monitor response to treatment. This innovative probe provides a promising tool to non-invasively study the unexplored roles of COL3 in cardiac fibrosis and other cardiovascular conditions marked by changes in COL3.
AB - Heart failure (HF) affects 64 million people globally with enormous societal and healthcare costs. Myocardial fibrosis, characterised by changes in collagen content drives HF. Despite evidence that collagen type III (COL3) content changes during myocardial fibrosis, in vivo imaging of COL3 has not been achieved. Here, we discovered the first imaging probe that binds to COL3 with high affinity and specificity, by screening candidate peptide-based probes. Characterisation of the probe showed favourable magnetic and biodistribution properties. The probe’s potential for in vivo molecular cardiac magnetic resonance imaging was evaluated in a murine model of myocardial infarction. Using the new probe, we were able to map and quantify, previously undetectable, spatiotemporal changes in COL3 after myocardial infarction and monitor response to treatment. This innovative probe provides a promising tool to non-invasively study the unexplored roles of COL3 in cardiac fibrosis and other cardiovascular conditions marked by changes in COL3.
KW - Molecular imaging
KW - Magnetic resonance imaging
KW - Chemical biology
KW - Fibrosis
KW - Imaging probes
U2 - 10.1038/s44303-024-00037-z
DO - 10.1038/s44303-024-00037-z
M3 - Article
SN - 2948-197X
JO - npj Imaging
JF - npj Imaging
ER -