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Biology subjects

Saiani, A.

Publications and source records attributed to Saiani, A..

2 recordsLinked to original sources

Generative Models Validation via Manifold Recapitulation Analysis

Comparing empirical distributions is central to generative model evaluation, hypothesis testing and data augmentation in high-dimensional biological data. Established methods such as energy distance summarize each point's relationship to the opposing distribution through a single expected distance, providing sensitivity to location shifts. We introduce Signature Distance (SD), a statistical distance that compares empirical distributions through the mean absolute difference of their sorted pointwise distance profiles. SD is a structural generalization of energy distance and matches its quadratic pairwise-distance cost, with an additional sorting step. In controlled experiments and on TCGA pan-cancer transcriptomic data, we show that (1) SD detects density changes with greater sensitivity than energy distance in the tested scale-contraction scenarios; (2) per-point mean-distance and signature-profile landscapes reveal the geometric mechanisms behind their different penalties; (3) linearly interpolated biological samples that receive no increased penalty from energy distance are penalized by SD; (4) SD provides a direct differentiable potential energy for model-free Langevin data expansion, with a bootstrap resampling protocol to assess the stopping epoch; and (5) SD is directly usable as a differentiable generative training loss. Code to reproduce all experiments is available at github.com/lazzaronico/signature-distance.

bioinformatics↗

Optimising a self-assembling peptide hydrogel as a Matrigel alternative for 3-dimensional mammary epithelial cell culture

Three-dimensional (3D) organoid models have been instrumental in understanding molecular mechanisms responsible for many cellular processes and diseases. However, established organic biomaterial scaffolds used for 3D hydrogel cultures, such as Matrigel, are biochemically complex and display significant batch variability, limiting reproducibility in experiments. Recently, there has been significant progress in the development of synthetic hydrogels for in vitro cell culture that are reproducible, mechanically tuneable, and biocompatible. Self-assembling peptide hydrogels (SAPHs) are synthetic biomaterials that can be engineered to be compatible with 3D cell culture. Here we investigate the ability of PeptiGel(R) SAPHs to model the mammary epithelial cell (MEC) microenvironment in vitro. The positively charged PeptiGel(R)Alpha4 supported MEC viability, but did not promote formation of polarised acini. Modifying the stiffness of PeptiGel(R) Alpha4 stimulated changes in MEC viability and changes in protein expression associated with altered MEC function, but did not fully recapitulate the morphologies of MECs grown in Matrigel. To supply the appropriate biochemical signals for MEC organoids, we supplemented PeptiGels(R) with laminin. Laminin was found to require negatively charged PeptiGel(R) Alpha7 for functionality, but was then able to provide appropriate signals for correct MEC polarisation and expression of characteristic proteins. Thus, optimisation of SAPH composition and mechanics allows tuning to support tissue-specific organoids.

cell biology↗