Soma-Targeted Imaging of Neural Circuits by Ribosome TetheringHighlights d Ribosome tethering restricts fluorescent proteins to the cell soma d A ribo-nanobody mouse boosts the fluorescence of existing GFP reporters d Ribo-GCaMP reduces fluorescence cross-contamination during 2P calcium imaging d Ribo-GCaMP enables whole-brain imaging of somatic calcium dynamics in the worm Authors

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In the present study, we investigated the mechanisms by which plasma lipoproteins modulate the integrindependent adhesion properties of monocytes. LDL induced the expression of the monocyte CD11b in vitro as well as in vivo via intracellular signaling mechanisms involving calcium transients. The effect on CD11b transcription was specific for native LDL and was blocked by a neutralizing anti-LDL receptor antibody. Neither oxidized LDL nor HDL had any effect on CD11b expression. Although LDL stimulated CD11b surface expression, the integrins were not activated. To initiate the CD11b-specific adhesion to the endothelium, the engagement of chemokine receptor CCR2 and intact chemokine-to-integrin signaling was necessary. However, the activation of CCR2 with monocyte chemoattractant protein-1 not only stimulated the integrins preexisting on the cell surface, but also increased the number of CD11b molecules on the cell surface. This was particularly pronounced in THP-1 cells after treatment with LDL. In a previous study, we showed that LDL induces the expression of CCR2 in monocytes. We conclude that this may be the underlying cause of the enhanced chemokine effect on CD11b expression and activation observed with these

: PEPT1 is a vital member of the proton-dependent oligopeptide transporters family (POTs). Many studies have confirmed that PEPT1 plays a critical role in the absorption of dipeptides, tripeptides, and pseudopeptides in the intestinal tract. In recent years, several studies have found that PEPT1 is highly expressed in malignant tumor tissues and cells. The abnormal expression of PEPT1 in tumors may be closely related to the progress of tumors, and hence, could be considered as a potential molecular biomarker for the diagnosis, treatment, and prognosis in malignant tumors. Furthermore, PEPT1 can be used as the delivery target to mediate the targeted delivery of antitumor drugs. Herein, the expression, regulation, and role of PEPT1 in tumors in recent years were reviewed.