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Extracellular vesicles (EVs) are biomarkers and mediators of intercellular communication. In biological samples, EVs are secreted by various types of cells. The proteomic identification of proteins expressed in EVs has potential to contribute to research and clinical applications, particularly for cancer. In this study, the proximity-labeling method-based proteomic approach was used for EV identification, labeling membrane components proximal to a given molecule on the EV membrane surface. Due to the small labeling range, proteins on the surface of the same EVs are likely to be labeled by selecting a given EV surface antigen. The protein group of cancer cell-secreted EV (cEV), which abundantly expresses a close homologue of L1 (CHL1), was examined using a model mouse for lung cancer (LC). cEV-expressed proteins were identified by proteomic analysis of enzyme-mediated activation of radical sources by comparing serum EVs from wild-type and LC mice. SLC4A1 was found to be co-expressed in CHL1-expressing EVs, highlighting EVs expressing both CHL1 and SLC4A1 as candidates for cEVs. Serum EVs expressing both CHL1 and caspase 14 were significantly elevated in LC patients compared with healthy individuals. Thus, the combination of proximity labeling and proteomic analysis allows for effective EV identification.

This study aims to investigate the vasorelaxation effects of a Rosa centifolia petal extract (ROSE CRYSTA®-70: ROSE-70) on the isolated aorta and the protective effect of ROSE-70 on human umbilical vein endothelial cells (HUVECs) dysfunction. ROSE-70 inhibited phenylephrine (PE) -induced contraction in an endothelium-dependent and endothelium-independent manner; however, this relaxation was lower in the endothelium-denuded aorta. ROSE-70-induced relaxation was attenuated by L-N

Extracellular vesicle (EV) has been investigated for use in clinical testing in recent years. Specific EV surface proteins provide distinguishing characteristics, but are insufficient for more detailed classification of EVs. Here, we suggest a novel “Bimolecular surface antigen expressed in EV” (BiEV) as a potential indicator for more efficient EV screening. A BiEV can be identified using a previously developed method, enzyme-mediated activation of radical sources, to label the components proximal (within 20 nm) to a given molecule. We examined the screening of cancer cell-secreted EV (cEV) included in serum EVs from a model mouse for lung cancer. The cEV-specific BiEVs were first identified by through a comparison of serum EVs from wild-type and lung cancer mice, showing that the CHL1-SLC4A1 bimolecule was a significant candidate for cEV-specific BiEV. Enzyme-linked immunosorbent assay quantification of CHL1-SLC4A1 BiEV appeared to suggest a potential for cancer screening of these mice. Using the same protocols, we found that CHL1-caspase 14 BiEV was significantly elevated in lung cancer patients compared with healthy persons. A BiEV strategy may be able to make a contribution to more effective EV screening, resulting in novel biological and clinical applications.

The swimming movement of Cryptomonas sp. cells generates a helical path, as a result of rotations with an average period of 500 milliseconds. When a flash of light at 570 nanometers for 20 microseconds was applied unidirectionally at intervals of 500 milliseconds, only a fixed side of each rotating cell was repeatedly exposed to the flashes of light. The relationship between the irradiated side of a cell and the phototactic orientation of the cell, rotating with a period of 475 to 525 milliseconds, was determined by infrared videomicrography. Only when the ventral sides of the cells were exposed to the flashes of light did their courses shift predominantly toward the light source. This result suggests that light is efficiently detected by the ventral side of these organisms.

The effect of Ca2+ ions on the phototactic orientation of Cryptomonas cells was determined by observation of the direction of swimming of individual cells using infrared video-micrography. When 2 mM EGTA was added to the medium, changes in the swimming direction of cells became smaller, consequently the phototactic orientation was inhibited. The EGTA-induced inhibition was almost completely overcome by the addition of 2 mM CaCl2. Consequently the presence of Ca2+ ions appears to be crucial for the orientation that is necessary during phototaxis of Cryptomonas cells.