“…Notably, an increased ACE2 presentation on the surface epithelium, blood vessels (endothelial), and supporting tissues (basement membrane, fibroblasts) in nearly all organs augment the rapid spread of circulatory SARS-CoV-2 in the body [ 34 ]. In addition to ACE2, SARS-CoV-2 can interact with a number of cellular proteins, namely dipeptidyl peptidase-4 (DPP4), CD147 (basigin), glucose-regulated protein (GRP78), angiotensin II type 2 receptor (AGTR2), and alanyl amino peptidase (ANPEP) and utilize co-receptors, such as neuropilin-1 (NRP-1), dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin 1 (DCSIGN1), cell adhesion molecule 5 (CEACAM5), heparin sulfate, and ganglioside GM1 [ 44 , 45 ]. NRP-1, a receptor for fur in-cleaved substrates, which is abundantly expressed in the respiratory tract, blood vessels, and neurons, has been shown to contribute to SARS-CoV-2 infectivity [ 46 ].…”