Non-Invasive whole-body detection of complement activation using radionuclide imaging in a mouse model of myocardial ischaemia-reperfusion injury

作者：Sharif Paghaleh Ehsan; Yap May Lin; Puhl Sarah Lena; Badar Adam; Torres Julia Baguna; Chuamsaamarkkee Krisanat; Kampmeier Florian; Smith Richard A; Clark James; Blower Philip J; Sacks Steven^*; Mullen Gregory E^*

来源：Scientific Reports, 2017, 7(1): 16090.

DOI：10.1038/s41598-017-16387-1

Complement activation is a recognised mediator of myocardial ischaemia-reperfusion-injury (IRI) and cardiomyocytes are a known source of complement proteins including the central component C3, whose activation products can mediate tissue inflammation, cell death and profibrotic signalling. We investigated the potential to detect and quantify the stable covalently bound product C3d by external body imaging, as a marker of complement activation in heart muscle in a murine model of myocardial IRI. We used single-photon-emission-computed-tomography (SPECT) in conjunction with (99m)Technecium-labelled recombinant complement receptor 2 (Tc-99m-rCR2), which specifically detects C3d at the site of complement activation. Compared to control imaging with an inactive CR2 mutant (Tc-99m-K41E CR2) or an irrelevant protein (Tc-99m-PSMA) or using Tc-99m-rCR2 in C3-deficient mice, the use of 99mTc-rCR2 in complement-intact mice gave specific uptake in the reperfused myocardium. The heart to skeletal muscle ratio of Tc-99m-rCR2 was significantly higher than in the three control groups. Histological analysis confirmed specific uptake of Tc-99m-rCR2. Following therapeutic inhibition of complement C3 activation, we found reduced myocardial uptake of Tc-99m-rCR2. We conclude, therefore that Tc-99m-rCR2 imaging can be used for non-invasive detection of activated complement and in future could be exploited to quantify the severity of myocardial damage due to complement activation.

• 出版日期2017-11-23