Search bioRxiv⌕ Search

Biology subjects

Alar, C.

Publications and source records attributed to Alar, C..

2 recordsLinked to original sources

SubCellSpace: Automated characterization of subcellular mRNA localization patterns in spatial transcriptomics

The localized translation of transcripts is a universal phenomenon across biological domains. Many examples of subcellular RNA localization and their functional importance have been described. However, these examples remain anecdotal, and a more systematic genome and cell-type-wide analysis is needed. Current spatial transcriptomic techniques can characterize hundreds to thousands of transcript species at subcellular resolutions, enabling the large-scale investigation of subcellular mRNA localization. Here we describe SubCellSpace, a computational framework to learn general representations of mRNA localization patterns. By embedding observed single-cell subcellular localization patterns (SLPs) to an interpretable latent space, SubCellSpace can detect and statistically infer the presence of SLPs, uncover colocalizing gene-pairs and characterize cellular heterogeneity for pattern-presentation. We benchmark SubCellSpace in both synthetic and real data, showing it can correctly detect previously described apical/basal polarized genes in the enterocytes of mouse small-intestine, as well as encode the enterocytes orientation. Additionally, we provide a tailored spatial transcriptomics validation dataset for benchmarking SLP identification based on transcripts previously described to be enriched near subcellular structures in HEK293T cells. We propose a practical and computationally-efficient classification workflow that automatically detects localized transcript species and quantifies their degree of patterning, while controlling false positive rates. Finally, we showcase SubCellSpace in both supervised and unsupervised settings, to either classify pre-determined SLPs or to explore spatial patterning without specifying pattern types a priori. Automated AI models such as SubCellSpace and their integration in spatial transcriptomics analysis workflows will help characterize previously undiscovered subcellular RNA localization phenomena, providing novel insights into post-transcriptional regulation mechanisms.

bioinformatics↗

Defining the role of fibroblasts in skin expansion

Stretch-mediated tissue expansion is commonly used to grow extra skin for reconstructive surgeries. To ensure harmonious growth, the two main skin compartments, the epidermis and the dermis, must both expand in a coordinated manner. Although the epidermal response has been previously described, it remains unclear how fibroblasts, the main supporting cell type, respond to stretching in vivo. Here we map the transcriptional response of the entire skin during stretch-mediated tissue expansion, and we describe the fibroblast response to stretching in vivo. We show an increase in fibroblast volume accompanied by changes in organisation. We demonstrate that stretching forces fibroblasts to exit their quiescent state and restart proliferation. Simultaneously, fibroblasts decrease their collagen content and increase the expression of specific extracellular matrix remodelling factors. By combining data from the in vivo stretching model and an in vitro keratinocyte-fibroblast co-culture system, we demonstrate that changes in fibroblasts promote the self-renewal of the epidermal stem cells, thus coordinating the response of these two compartments during skin expansion. These findings provide valuable insights to guide the design of in vivo stretch-mediated tissue expansion protocols and the production of in vitro skin grafts for clinical application.

cell biology↗