MorphoCLIP: Text-Supervised Contrastive Learning for Perturbation Matching in Cell Painting Images

Understanding fluorescence microscopy images is fundamental to automating biological research. However, existing methods typically learn predefined concepts from closed-set data, limiting transfer across tasks and biological contexts. In this work, we introduce MicroCLIP, a vision-language model that learns generalizable cellular and subcellular representations from natural language supervision for open-set image classification and retrieval. To pretrain MicroCLIP, we construct MicroPool-2M, a dataset of approximately 2.5 million fluorescence microscopy image-text pairs spanning diverse cellular structures, cell lines, and imaging conditions. Aligning microscopy images with biological concepts in natural language is challenging because most images lack descriptive captions and biological knowledge annotations. We therefore progressively establish image-text associations at three levels to provide MicroCLIP with richer semantic supervision: (1) category-level alignment links images to standardized labels defined by subcellular structure-cell-line combinations; (2) knowledge-level alignment incorporates biological priors derived from these labels to capture relationships across species and cell types; and (3) detail-level alignment uses a multimodal large language model to recaption and verify image-text pairs at scale, emphasizing fine-grained visual characteristics. Extensive experiments demonstrate that MicroCLIP achieves leading performance in zero-shot classification and text-image retrieval on microscopy images. It retrieves images with specific cellular characteristics from thousands of candidates and generalizes to unseen biological concepts without additional supervision. These results highlight MicroCLIP's potential as a foundation model for fluorescence microscopy.

Cell Painting combines multiplexed fluorescent staining, high-content imaging, and quantitative analysis to generate high-dimensional phenotypic readouts to support diverse downstream tasks such as mechanism-of-action (MoA) inference, toxicity prediction, and construction of drug-disease atlases. However, existing workflows are slow, costly and difficult to interpret. Approaches for drug screening modeling predominantly focus on molecular representation learning, while neglecting actual experimental context (e.g., cell line, dosing schedule, etc.), limiting generalization and MoA resolution. We introduce CP-Agent, an agentic multimodal large language model (MLLM) capable of generating mechanism-relevant, human-interpretable rationales for cell morphological changes under drug perturbations. At its core, CP-Agent leverages a context-aware alignment module, CP-CLIP, that jointly embeds high-content images and experimental metadata to enable robust treatment and MoA discrimination (achieving a maximum F1-score of 0.896). By integrating CP-CLIP outputs with agentic tool usage and reasoning, CP-Agent compiles rationales into a structured report to guide experimental design and hypothesis refinement. These capabilities highlight CP-Agent's potential to accelerate drug discovery by enabling more interpretable, scalable, and context-aware phenotypic screening -- streamlining iterative cycles of hypothesis generation in drug discovery.

Cell Painting is a high-content morphological profiling assay widely used for phenotype-based biological inference, with mechanism of action (MOA) prediction as a central application. Existing approaches largely formulate Cell Painting-based inference as representation matching, assigning predictions from nearby reference perturbations in morphological feature space. However, retrieved neighbors are often noisy and partially misleading evidence due to batch effects, non-specific cytotoxicity, phenotypic convergence, and source-dependent variability. We reformulate Cell Painting-based MOA prediction as a calibrated evidence reasoning problem, where retrieved neighbors are treated as uncertain observations that must be evaluated, compared, and sometimes rejected before supporting a mechanistic conclusion. We propose PhenoAIR, a reliability-aware multi-agent framework that maintains a candidate-centric evidence memory and performs controller-guided refinement over phenotype- and mechanism-side evidence. PhenoAIR uses offline reference-set calibration to weight evidence by source reliability, phenotype stability, and mechanism-level confusion. We evaluate PhenoAIR on a benchmark constructed from JUMP Cell Painting profiles and annotations, covering controlled, realistic, and discovery-oriented open-world MOA prediction settings. PhenoAIR outperforms representation-matching and LLM-based baselines across all settings.