Biology subjects

Dominguez Mantes, A.

Publications and source records attributed to Dominguez Mantes, A..

3 recordsLinked to original sources

bioRxiv2024

Specialized signaling centers direct cell fate and spatial organization in a limb organoid model

Specialized signaling centers orchestrate robust development and regeneration. Limb morphogenesis, for instance, requires interactions between the mesoderm and the signaling center apical-ectodermal ridge (AER), whose properties and role in cell fate decisions have remained challenging to dissect. To tackle this, we developed mouse embryonic stem cells (mESCs)-based heterogeneous cultures and a limb organoid model, termed budoids, comprising cells with AER, surface ectoderm, and mesoderm properties. mESCs were first induced into heterogeneous cultures that self-organized into domes in 2D. Aggregating these cultures resulted in formation of limb bud-like structures in 3D, exhibiting chondrogenesis-based symmetry breaking and elongation. Using our organoids and quantitative in situ expression profiling, we uncovered that AER-like cells support nearby limb mesoderm and fibroblast identities while enhancing tissue polarization that permits distant cartilage formation. Together, our findings provide a powerful model to study aspects of limb morphogenesis, and reveal the ability of signaling center AER cells to concurrently modulate cell fate and spatial organization.

developmental biology↗

bioRxiv2024

Spotiflow: accurate and efficient spot detection for imaging-based spatial transcriptomics with stereographic flow regression

Identifying spot-like structures in large and noisy microscopy images is a crucial step to produce high quality results in various life-science applications. Imaging-based spatial transcriptomics (iST) methods, in particular, critically depend on the precise detection of millions of transcripts in images with low signal-to-noise ratio. Despite advances in computer vision that have revolutionized many biological imaging tasks, currently adopted spot detection techniques are mostly still based on classical signal processing methods that often lack robustness to changing imaging conditions and thus require tedious manual tuning per dataset. In this work, we introduce Spotiflow, a deep learning method that achieves subpixel-accurate localizations by formulating the spot detection task as a multi-scale heatmap and stereographic flow regression problem. Spotiflow can be used for 2D images and 3D volumetric stacks and can be trained to generalize across different imaging conditions, tissue types and chemical preparations, while being substantially more time- and memory-efficient than existing methods. We show the efficacy of Spotiflow via extensive quantitative experiments on a variety of diverse datasets and demonstrate that the enhanced accuracy of SO_SCPLOWPOTIFLOWC_SCPLOW leads to meaningful improvements in the biological insights obtained from iST and live imaging experiments. Spotiflow is available as an easy-to-use Python library as well as a napari plugin at https://github.com/weigertlab/spotiflow.

bioinformatics↗

bioRxiv2024

Statistical inference with a manifold-constrained RNA velocity model uncovers cell cycle speed modulations

Across a range of biological processes, cells undergo coordinated changes in gene expression, resulting in transcriptome dynamics that unfold within a low-dimensional manifold. Single-cell RNA-sequencing (scRNA-seq) only measures temporal snapshots of gene expression. However, information on the underlying low-dimensional dynamics can be extracted using RNA velocity, which models unspliced and spliced RNA abundances to estimate the rate of change of gene expression. Available RNA velocity algorithms can be fragile and rely on heuristics that lack statistical control. Moreover, the estimated vector field is not dynamically consistent with the traversed gene expression manifold. Here, we develop a generative model of RNA velocity and a Bayesian inference approach that solves these problems. Our model couples velocity field and manifold estimation in a reformulated, unified framework, so as to coherently identify the parameters of an autonomous dynamical system. Focusing on the cell cycle, we implemented VeloCycle to study gene regulation dynamics on one-dimensional periodic manifolds and validated using live-imaging its ability to infer actual cell cycle periods. We benchmarked RNA velocity inference with sensitivity analyses and demonstrated one- and multiple-sample testing. We also conducted Markov chain Monte Carlo inference on the model, uncovering key relationships between gene-specific kinetics and our gene-independent velocity estimate. Finally, we applied VeloCycle to in vivo samples and in vitro genome-wide Perturb-seq, revealing regionally-defined proliferation modes in neural progenitors and the effect of gene knockdowns on cell cycle speed. Ultimately, VeloCycle expands the scRNA-seq analysis toolkit with a modular and statistically rigorous RNA velocity inference framework.

systems biology↗