Key result
CSO-PAA-Fe3O4 nanoprobes inhibit macrophage foaming, reducing cholesterol ~44% and enabling targeted MRI.
Why the study?
Molecular imaging techniques for early localization and diagnosis of atherosclerosis plaques and inhibition of macrophage foam cell formation by chitooligosaccharides were under investigation.
p-value: p=<0.05
The CSO-PAA-Fe3O4 nanoprobe demonstrates potential as a targeted MRI contrast agent for macrophages and an inhibitor of foam cell formation in in vitro atherosclerosis models.
Hypothesis-generating for macrophage-targeted MRI in atherosclerosis; leaves open clinical translation pending in vivo validation.
Atherosclerosis (AS) is a primary cause of morbidity and mortality all over the world. Molecular imaging techniques can enable early localization and diagnosis of atherosclerosis plaques. Recent newly developed chitooligosaccharides (CSO) is considered to be capable of target mannose receptors on the surface of macrophages and to inhibit foam cell formation. Here we present a targeting magnetic resonance imaging (MRI) nanoprobe, which was successfully constructed with polyacrylic acid (PAA) modified nanometer iron oxide (Fe3O4) as the core, and coating with CSO molecules, possessing the abilities of targeted MRI and specifically inhibition of the formation of foamy macrophages in the atherosclerotic process. The experimental results showed that the distributions of PAA-Fe3O4 and CSO-PAA-Fe3O4 were uniform and the corresponding sizes were about 5.93 nm and 8.15 nm, respectively. The Fourier transform infrared spectra (FTIR) testified the CSO was coupled with PAA-Fe3O4 successfully. After coupled with CSO, the r1 of PAA-Fe3O4 was increased from 5.317 mM s-1 to 6.147 mM s-1, indicating their potential as MRI contrast agent. Oil Red O staining and total cholesterols (TC) determination showed that CSO-PAA-Fe3O4 could significantly inhibit the foaming process of RAW264.7 cells induced by oxidatively modified low density lipoprotein (ox-LDL). In vitro cellular MRI displayed that, compared with PAA-Fe3O4,CSO-PAA-Fe3O4 could lower the T1 relaxation time of RAW264.7 cells better. In summary, construction of CSO-PAA-Fe3O4 nanoprobe in this study could realize the targeted MRI of macrophages and inhibition of ox-LDL induced macrophage foaming process. This will provide a new avenue in the diagnosis and treatment of AS.
No takes yet. Share an insight, caveat, or question.
Cao et al. (2021) studied Atherosclerosis. CSO-PAA-Fe3O4 nanoprobe vs. PAA-Fe3O4 nanoprobe was evaluated on Total cholesterol (TC) content in RAW264.7 cells (p=<0.05). CSO-PAA-Fe3O4 nanoprobes significantly inhibited ox-LDL induced macrophage foaming, reducing total cholesterol content to 56.5% at 0.35 mmol/L, and provided targeted T1-weighted MRI capability.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: