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Patili, E.

Publications and source records attributed to Patili, E..

2 recordsLinked to original sources

imAgeScore, a Cell Painting-Based Predictor of Cellular Age for High-throughput Drug Screening Applications

Quantifying cellular age in vitro in a scalable and biologically meaningful manner is essential for the discovery of pharmacological interventions that modulate aging. We developed imAgeScore, a machine-learning model trained on high-content Cell Painting features to predict the phenotypic age of primary human dermal fibroblasts. imAgeScore correlates with chronological and DNA methylation-based age estimates and captures coordinated morphological changes across nuclear and cytoplasmic compartments. The model detected age acceleration during serial propagation and age reduction following partial reprogramming. Pharmacological interventions targeting distinct aging hallmarks induced predictable shifts in predicted age and enabled classification of damaging versus rejuvenating cellular states. Application of imAgeScore in an automated high-throughput screening pipeline identified candidate age-modulating compounds, revealed inter-individual variability in response magnitude, and detected additive rejuvenation effects in selected combinatorial treatments. Functional validation in a scratch wound assay confirmed enhanced cellular repair by leading candidates, supporting the biological relevance of morphology-derived age reduction. Together, these results demonstrate that image-based morphological profiling provides a scalable platform for quantifying cellular aging and screening for candidate rejuvenation interventions.

cell biology↗

Single step, high efficiency CRISPR-Cas9 genome editing in primary human disease-derived fibroblasts

Genome editing is a tool that has many applications including the validation of potential drug targets. However, performing genome editing in low passage, primary human cells with the greatest physiological relevance, is notoriously difficult. High editing efficiency is desired because it enables gene knock outs (KO) to be generated in bulk cellular populations and circumvents the problem of having to generate clonal cell isolates. Here, we describe a single step workflow enabling >90% KO generation in primary human lung fibroblasts via CRISPR ribonucleoprotein delivery, in the absence of antibiotic selection or clonal expansion. As proof of concept, we performed a disease relevant phenotypic assay measuring collagen deposition in response to TGF{beta} and demonstrated SMAD3 but not SMAD2 dependent deposition of type I collagen following knockout of each using our single step methodology. The optimization of this workflow can readily be transferred to other primary cell types.

molecular biology↗