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Biology subjects

Chen, R.-H.

Publications and source records attributed to Chen, R.-H..

2 recordsLinked to original sources

Hybrid Neural Networks of the Olfactory Learning Center in the Drosophila Brain

Biological signal encoding is shaped by the underlying neural circuitry. In Drosophila melanogaster, the mushroom body (MB) houses thousands of Kenyon cells (KCs) that process olfactory signals from hundreds of projection neurons (PNs). Previous studies debated the connectivity between PNs and KCs (random vs. structured). Our multiscale analysis of electron microscopic data revealed a hybrid network with diverse synaptic connection preferences and input divergence across different KC classes. Using MB connectome data, our simulation model, validated via functional imaging, accurately predicted distinct chemical sensitivities in the major KC classes. The model suggests that the hybrid network excels in detecting food odors while maintaining precise odor discrimination in different KC classes. These findings underscore the computational advantages of this hybrid network.

neuroscience↗

Membrane Protein Modification Modulates Big and Small Extracellular Vesicle Biodistribution and Tumorigenic Potential in Breast Cancers In Vivo

Extracellular vesicles (EVs) are released by cells to mediate intercellular communication under pathological and physiological conditions. While small EVs (sEVs; <100-200 nm, exosomes) are intensely investigated, the properties and functions of medium and large EVs (big EVs [bEVs]; >200 nm, microvesicles) are less well explored. Here, we identify bEVs and sEVs as distinct EV populations, and determine that bEVs are released in a greater bEV:sEV ratio in the aggressive human triple-negative breast cancer (TNBC) subtype. PalmGRET, bioluminescence resonance energy transfer (BRET)-based EV reporter, reveals dose- dependent EV biodistribution at non-lethal and physiological EV dosages, as compared to lipophilic fluorescent dyes. Remarkably, the bEVs and sEVs exhibit unique biodistribution profiles, et individually promote in vivo tumor growth in a syngeneic immunocompetent TNBC breast tumor murine model. The bEVs and sEVs share mass spectrometry (MS)- identified tumor progression-associated EV surface membrane proteins (tpEVSurfMEMs), which include SLC29A1, CD9 and CD44. tpEVSurfMEM depletion attenuates EV lung organotropism, alters biodistribution, and reduces protumorigenic potential. This study identifies distinct in vivo property and function of bEVs and sEVs in breast cancer, which suggest the significant role of bEVs in diseases, diagnostic and therapeutic applications.

cancer biology↗