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Updated: Jan 1, 2026

Author Spotlight: A Pipeline to Analyze Lineage-Specific Mutant Embryos at Single-Cell Resolution
Published on: June 14, 2024
Single cell RNA-sequencing reveals cellular heterogeneity and trajectories of lineage specification during murine
Natalie H Kelly1, Nguyen P T Huynh2, Farshid Guilak1
1Department of Orthopaedic Surgery, Washington University, 4515 McKinley Ave, St. Louis, MO, 63110, USA; Shriners Hospital for Children - St. Louis, 4400 Clayton Ave, St. Louis, MO, 63110, USA; Center of Regenerative Medicine, Washington University, St. Louis, MO, 63110, USA.
Abstract:
The coordinated spatial and temporal regulation of gene expression in the murine hindlimb determines the identity of mesenchymal progenitors and the development of diversity of musculoskeletal tissues they form. Hindlimb development has historically been studied with lineage tracing of individual genes selected a priori, or at the bulk tissue level, which does not allow for the determination of single cell transcriptional programs yielding mature cell types and tissues. To identify the cellular trajectories of lineage specification during limb bud development, we used single cell mRNA sequencing (scRNA-seq) to profile the developing murine hindlimb between embryonic days (E)11.5-E18.5. We found cell type heterogeneity at all time points, and the expected cell types that form the mouse hindlimb. In addition, we used RNA fluorescence in situ hybridization (FISH) to examine the spatial locations of cell types and cell trajectories to understand the ancestral continuum of cell maturation. This data provides a resource for the transcriptional program of hindlimb development that will support future studies of musculoskeletal development and generate hypotheses for tissue regeneration.

