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Jun, L.

Publications and source records attributed to Jun, L..

3 recordsLinked to original sources

Microdomes: Micro-engineered Microdome arrays enable standardised and shear-free 3D biology with full-spectrum optical imaging compatibility

Three-dimensional cellular models such as organoids and spheroids hold major promise for developmental biology, disease modelling and precision medicine, yet their large-scale production and analysis remain constrained by handling-induced shear stress, sample fragility, positional instability and limited compatibility with advanced imaging workflows. Here, we introduce Microdomes, dense arrays of open-top, dome-shaped microcavities. Each cavity holds a single specimen in its own miniature aquarium, accessed through a narrow apical opening that admits cells, medium, matrix and staining reagents while shielding it from the shear generated during routine pipetting. Each Microdomes chip accommodates more than 100 spheroids or organoids, supporting diverse cell types, co-culture formats and both matrix-free and matrix-embedded culture. All specimens are retained through prolonged culture, repeated medium exchange, fixation and immunostaining. Because every specimen occupies a fixed, addressable position against a thin transparent film, the same spheroid can be relocated and re-imaged over weeks of culture and across microscopes, from array-wide overviews to subcellular details, without transfer, embedding or other perturbation. Microdomes also support AI-based automated segmentation, from whole-spheroid outlines to individual nuclei in 3D, using common image analysis software. Microdomes thereby turn each array into a self-contained quality control unit, providing specimen-level traceability that organoid production pipelines currently lack.

cell biology↗

A High-Resolution N-Glycoproteome Atlas Reveals Tissue-Specific Glycan Remodeling but Non-random Structural Microheterogeneities

The mouse is a widely used model organism in biomedical research, yet a comprehensive understanding of its tissue-specific glycoproteome has been limited due to the structural complexity and microheterogeneity of glycans. Here, we present the most extensive high-resolution N-glycoproteomic atlas across 24 mouse tissues, which comprises of 3,045 N-glycans with distinct structures attached at 8,681 glycosites on 74,277 glycopeptides and 5,026 glycoproteins. Overall glycan structural patterns show enormous tissue-specific diversities, acting as superior molecular signatures of tissue identity and system origins. Notably, even commonly expressed glycoproteins undergo tissue-dependent glycan remodeling, suggesting that glycosylation may fine-tune protein functions to meet specialized biological demands. These patterns are further shaped by subcellular localization, which constrains glycan variabilities across compartments. Co-occurrence network analyses also expose substructural biases and non-random microheterogeneities among glycans attached at the same glycosites. The dataset serves as a valuable database resource for advancing the structural and functional understanding of glycoproteins.

biochemistry↗

miR-206 inhibits estrogen-induced proliferation and invasion of ER-α36 positive gastric cancer cells

ObjectiveTo explore the biological role of miR-206 in inhibiting the proliferation and invasion of estrogen-induced ER-36 positive gastric cancer cells and its related mechanisms. MethodsMTT and tranwell assays were used to detect the proliferation and invasion of BGC-823 cells under different concentrations and time of ER stimulation. RT-PCR was used to detect the effect of ER stimulation on the content of miR-206 in gastric cancer cells. miR-206 mimics were transfected into BGC-823 cells to detect cell proliferation and invasion; luciferase reporter assay was used to determine whether miR-206 targets the 3-untranslated region of the CDK14-encoding gene (3 -UTR). ResultsWe confirmed that estrogen promoted the proliferation and invasion of BGC-823 cells; As the concentration of estrogen increases, the level of miR206 in the cell gradually rises.Overexpression of miR-206 significantly decreased the estrogen-induced BGC-823 cells. Proliferative and invasive ability; miR-206 inhibits the expression of CDK14 by directly binding to the 3-UTR of CDK14 mRNA, thereby inhibiting the proliferation and invasion of gastric cancer cells. ConclusionsOur results suggest that miR-206 inhibits estrogen-induced proliferation and invasion of ER-36-positive gastric cancer cells by inhibiting CDK14 and may be a promising therapeutic option for anticancer therapy.

cancer biology↗