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Biology subjects

Cho, S. E.

Publications and source records attributed to Cho, S. E..

2 recordsLinked to original sources

AI-enabled discovery of small molecules targeting complementary pathways for hair follicle rejuvenation

Hair thinning arises from multi-faceted dysfunction within the hair follicle, driven by both intrinsic cellular pathways and pathways responding to extrinsic hormonal and microenvironmental cues. Here, we present an AI-enabled discovery framework to discover small molecules that promote hair follicle rejuvenation. This framework integrates graph neural networks trained on phenotypic screening data with structure-based virtual screening to prioritize compounds that modulate complementary biological pathways. Through AI-enabled screening, hit-to-lead optimization, and medicinal chemistry, we identified four compounds that increase follicle dermal papilla cell viability, stabilize hypoxia signaling by inhibiting prolyl hydroxylase domain protein 2 (PHD2), and suppress androgen-mediated follicular miniaturization by inhibiting 5-reductases (5-ARs). RNA sequencing analyses confirmed pathway engagement, and functional validation across primary cells and a 3D hair follicle organoid model demonstrated high activity and cellular specificity. The lead compounds were incorporated into a water-based formulation, where they demonstrated robust solubility and combinatorial efficacy to increase sprouting length of follicle organoids. These results establish an AI-enabled platform for discovering multi-pathway modulators of hair follicle rejuvenation.

bioengineering↗

DILP8 serves as a mature follicle sensor to prevent excessive accumulation of maturefollicles in Drosophila ovaries and oocyte aging.

Excessive mature follicle accumulation in ovaries harms oocyte health and offspring viability. As such, the number of mature follicles in ovaries is tightly controlled. In Drosophila, each ovary is comprised of [~]16 ovarioles, each containing 1-2 mature follicles, regardless of the females mating status. The mechanism by which the female flies count the number of mature follicles to coordinate egg release and oogenesis remains a mystery. Previous work, along with our RNAseq and antibody analysis, demonstrated that Drosophila insulin-like peptide 8 (DILP8) is expressed in somatic follicle cells of mature follicles but not in younger follicles. Contrary to previous findings, we found that DILP8 is not essential for mating-induced ovulation/egg laying. In contrast, global depletion or follicle-cell-specific knockdown of dilp8 leads to defective ovulation/egg laying and a significant increase of mature follicles in virgin females. In addition, we found that excessive accumulation of mature follicles in dilp8-knockdown females leads to poor oocyte quality. Furthermore, knockdown of Lgr3 (Leucine-rich repeat-containing G protein-coupled receptor 3), encoding a previously identified DILP8 receptor, showed similar ovulation/egg laying defects, accumulation of mature follicles, and poor oocyte quality in virgin females. Therefore, DILP8 functions as a mature follicle sensor to prevent excessive accumulation of mature follicles and maintain oocyte quality through the Lgr3 receptor in virgin females. Because mating is not always available in the wild and the DILP8/Lgr3 pathway is highly conserved across multiple species, our findings suggest that DILP8/Lgr3 is likely critical for maintaining the optimal reproductive fitness of virgin females and for species survival in the wild.

physiology↗