Single-Cell and Spatial Transcriptome Analysis of Dermal Fibroblast Development in Perinatal Mouse Skin: Dynamic Lineage Differentiation and Key Driver Genes

• Published in: Journal of investigative dermatology Vol. 144; no. 6; pp. 1238 - 1250.e11
• Main Authors: Lee, Hanjae, Kim, So Young, Kwon, Nak-Jung, Jo, Seong Jin, Kwon, Ohsang, Kim, Jong-Il
• Format: Journal Article
• Language: English
• Published: United States 01.06.2024
• Subjects: Spatial analysis; Differentiation; Developmental biology; Single-cell analysis; Fibroblast
• ISSN: 0022-202X; 1523-1747
• DOI: 10.1016/j.jid.2023.11.008

Several single-cell RNA (scRNA) studies of developing mouse skin have elucidated the molecular and cellular processes involved in skin development. However, they have primarily focused on either the fetal or early postnatal period, leaving a gap in our understanding of skin development. Here, we conducted a comprehensive time-series analysis by combining scRNA sequencing datasets collected at different stages of development (embryonic days 13.5, 14.5, and 16.5 and postnatal days 0, 2, and 4) and validated our findings through multi-panel in situ spatial transcriptomics. Our analysis indicated that embryonic fibroblasts exhibit heterogeneity from a very early stage and that the rapid determination of each lineage occurs within days after birth. The expression of putative key driver genes, including Hey1, Ebf1, Runx3, and Sox11 for the dermal papilla trajectory, Lrrc15 for the dermal sheath trajectory, Zfp536 and Nrn1 for the papillary fibroblast trajectory, and Lrrn4cl and Mfap5 for the fascia fibroblast trajectory, was detected in the corresponding, spatially identified cell types. Lastly, cell-to-cell interaction analysis indicated that the dermal papilla lineage is the primary source of the non-canonical Wnt pathway during skin development. Together, our study provides a transcriptomic reference for future research in the field of skin development and regeneration.