<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>31</volume><submitter>Zhang Z</submitter><funding>National Natural Science Foundation of China</funding><funding>Liaoning Provincial Natural Science Foundation</funding><pubmed_abstract>The underlying mechanisms governing the interactions between nanoparticles and vascular endothelial barrier remain largely unexplored, which is crucial for the optimal design of nanoparticles for clinical applications. In this study, the size-dependent interactions between calciprotein particles (CPPs) and endothelial cells (ECs) were investigated using a rat model of chronic kidney disease (CKD) induced by 5/6 nephrectomy. Two primary types of CPP1 were studied: small-sized CPP1 (S-CPP1, &lt;50 nm) and larger CPP1 (L-CPP1, &lt;100 nm), detected three and five weeks post-surgery, respectively. By adjusting the amounts of Ca&lt;sup>2+&lt;/sup>, HPO&lt;sub>4&lt;/sub> &lt;sup>2-&lt;/sup> and H&lt;sub>2&lt;/sub>PO&lt;sub>4&lt;/sub> &lt;sup>-&lt;/sup> ions in Dulbecco's Modified Eagle Medium supplemented with 10 % (V/V) fetal bovine se</pubmed_abstract><journal>Materials today. Bio</journal><pagination>101599</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11894339</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Size-dependent interactions between calciprotein particles and vascular endothelium.</pubmed_title><pmcid>PMC11894339</pmcid><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Huang C</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Hao L</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Cui W</pubmed_authors><pubmed_authors>Yang R</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang HH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Size-dependent interactions between calciprotein particles and vascular endothelium.</name><description>The underlying mechanisms governing the interactions between nanoparticles and vascular endothelial barrier remain largely unexplored, which is crucial for the optimal design of nanoparticles for clinical applications. In this study, the size-dependent interactions between calciprotein particles (CPPs) and endothelial cells (ECs) were investigated using a rat model of chronic kidney disease (CKD) induced by 5/6 nephrectomy. Two primary types of CPP1 were studied: small-sized CPP1 (S-CPP1, &lt;50 nm) and larger CPP1 (L-CPP1, &lt;100 nm), detected three and five weeks post-surgery, respectively. By adjusting the amounts of Ca&lt;sup>2+&lt;/sup>, HPO&lt;sub>4&lt;/sub> &lt;sup>2-&lt;/sup> and H&lt;sub>2&lt;/sub>PO&lt;sub>4&lt;/sub> &lt;sup>-&lt;/sup> ions in Dulbecco's Modified Eagle Medium supplemented with 10 % (V/V) fetal bovine se</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2025-04-04T02:54:29.5Z</modification><creation>2025-04-04T02:54:29.5Z</creation></dates><accession>S-EPMC11894339</accession><cross_references><pubmed>40070870</pubmed><doi>10.1016/j.mtbio.2025.101599</doi></cross_references></HashMap>