Single-nucleus transcriptional and chromatin accessibility analyses of maturing mouse Achilles tendon uncover the molecular landscape of tendon stem/progenitor cells

  1. Hiroki Tsutsumi
  2. Tomoki Chiba
  3. Yuta Fujii
  4. Takahide Matsushima
  5. Tsuyoshi Kimura
  6. Akinori Kanai
  7. Akio Kishida
  8. Yutaka Suzuki
  9. Hiroshi Asahara  Is a corresponding author
  1. Department of Systems BioMedicine, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Japan
  2. Department of Molecular and Cellular Biology, The Scripps Research Institute, United States
  3. Laboratory for Biomaterials and Bioengineering, Institute of Integrated Research, Institute of Science Tokyo, Japan
  4. Department of Biomedical Engineering, Faculty of Life Science, Toyo University, Japan
  5. Laboratory of Systems Genomics, Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Japan
5 figures, 1 table and 18 additional files

Figures

Figure 1 with 3 supplements
Single-cell RNA sequencing (scRNA-seq) of tendon cells from 2-week-old and 6-week-old mice and the identification of surface markers of tendon stem/progenitor cell (TSPC).

(A) Integrated uniform manifold approximation and projection (UMAP) scRNA-seq clustering of cells harvested from 2-week-old and 6-week-old mouse Achilles tendons. (B) Dot plot of average gene expression levels of the indicated genes in each scRNA-seq cluster. The size of the dot reflects the percentage of cells in the cluster that express each gene. TC, tenocyte; SP1, tendon stem/progenitor cell_1; CA, cartilage; RB, ribosomal RNA; SP2, tendon stem/progenitor cell_2; LC1, lymphocyte_1; EC, endothelial cell; RBC, red blood cell; SM, smooth muscle cell; PC, proliferating cell; LC2, lymphocytes_2; MTJ, myotendinous junction cell; SW, Schwann cell; VEC, vascular endothelial cell; MC, macrophage. (C) Proportions of cells in clusters identified from scRNA-seq. Clusters are colored according to cluster type. (D) Volcano plot of gene expression in the SP2 cluster and the identification of candidate TSPC marker genes (red under line). (E) Feature plot of Cd55 and Cd248 expression. (F) Correlation of gene expression of TSPC candidate genes in 2-week data. (G) Violin plots presenting the gene expression changes for a selection of differentially expressed genes.

Figure 1—figure supplement 1
2-Week and 6-week single-cell RNA sequencing (scRNA-seq) results.

(A) Integrated uniform manifold approximation and projection (UMAP) scRNA-seq clustering of cells harvested from 2-week-old and 6-week-old mouse Achilles tendons. Clusters are colored according to cluster type. (B) Feature plot of Tppp3, Pdgfra, and Ly6a expression.

Figure 1—figure supplement 2
Comparison of 2-week and 6-week single-cell RNA sequencing (scRNA-seq) results.

(A) Violin plot of gene expression enriched in the limb bud (Development (2014) 141, 3683–3696) in each cluster. (B) Gene Ontology (GO) terms associated with genes with upregulated expression in the SP2 cluster. (C) Number of inferred interactions and interaction strength of genes expressed within 2-week and 6-week mouse scRNA-seq data.

Figure 1—figure supplement 3
Comparative analysis of 2-week and 6-week single-cell RNA sequencing (scRNA-seq) results.

Heatmap showing differential gene expression between red (2 weeks) and green (6 weeks).

Figure 2 with 2 supplements
snATAC-seq of tendon cells from a 2-week-old mouse and the validation of Cd55 and Cd248 as candidate markers of tendon stem/progenitor cell (TSPC).

(A) Uniform manifold approximation and projection (UMAP) snATAC-seq clustering of cells derived from the Achilles tendon of a 2-week-old mouse. Annotation was based on each gene activity (ground-truth annotation). SP1, tendon stem/progenitor cell_1; TC1, tenocyte_1; MTJ, myotendinous junction cell; SM, smooth muscle cell; MC, macrophage; CA, cartilage; TC2, tenocyte_2; SK, skeletal muscle cell; SW, Schwann cell; LC, lymphocyte; NC, neutrophil; EC, endothelial cell; RBC, red blood cell; UC, unspecified cell; SP2, tendon stem/progenitor cell_2; SP3, tendon stem/progenitor cell_3; VEC, vascular endothelial cell. (B) Dot plot of average gene activity of the indicated genes in each snATAC-seq cluster. The size of the dot reflects the percentage of cells in the cluster that express each gene. (C) UMAP visualization and predicted annotation of 2-week snATAC-seq after integration and label transfer of 2-week snRNA-seq data. (D) Identification of matching cell clusters between the 2-week snRNA- and 2-week snATAC-seq data from visualized as heatmap. The heatmap shows the proportions of cells from each snATAC-seq cluster across all sample conditions assigned to each snRNA-seq cluster as part of the label-transfer process. (E) Violin plot of tenocytes and TSPC-related gene expression in each cluster.

Figure 2—figure supplement 1
Analysis of 2-week snRNA-seq data.

(A) Uniform manifold approximation and projection (UMAP) snRNA-seq clustering of cells harvested from 2-week mouse Achilles tendons. (B) Dot plot of average gene expression levels of the indicated genes in 2-week snRNA-seq clusters. RB, ribosomal RNA; TC1, tenocyte_1; SP1, stem/progenitor cell_1; SP2, stem/progenitor cell_2; SM, smooth muscle cell; MTJ, myotendinous junction cell; CA, cartilage; SP3, stem/progenitor cell_3; LC, lymphocyte; MC, macrophage; RBC, red blood cell; SW, Schwann cell; EC, endothelial cell; TC2, tenocyte_2; PC, proliferating cell; NC, neutrophil; UC, unspecified cell. (C) Violin plot of tenocytes and tendon stem/progenitor cell (TSPC)-related gene expression in each cluster. (D) Feature plot of TSPC-related gene expression.

Figure 2—figure supplement 2
Analysis of 6-week snATAC-seq.

(A) Uniform manifold approximation and projection (UMAP) snATAC-seq clustering of cells harvested from 6-week mouse Achilles tendons. Annotation was based on gene activity (ground-truth annotation, left) and the predicted annotation inferred from 2-week snATAC-seq (right). (B) Identification of matching cell clusters between the 2-week and 6-week snATAC-seq data, visualized as a heatmap. lin plot of tenocytes and tendon stem/progenitor cell (TSPC)-related gene activity in each cluster.

Figure 3 with 3 supplements
Trajectory analysis and peak visualization of snRNA-seq and snATAC-seq data for the tendon and tendon stem/progenitor cell (TSPC)-related cluster.

(A) Uniform manifold approximation and projection (UMAP) representation of snRNA-seq differentiation trajectory of tenocytes and TSPC lineage and pseudotime-dependent gene expression changes of Tppp3, Cd55, Cd248, Mkx, and Scx, as inferred using Monocle3. (B) UMAP representation of snATAC-seq differentiation trajectory of tenocytes and the TSPC lineage and pseudotime-dependent gene expression changes, as inferred using Cicero. (C) Coverage plots of Mkx, Scx, Cd55, and Cd248. Selected peaks that differ across each cluster are highlighted.

Figure 3—figure supplement 1
Comparison of snRNA-seq and single-cell RNA sequencing (scRNA-seq).

(A) Dot plot of representative differentially expressed genes (DEGs) in snRNA-seq (2 weeks) and snRNA-seq (2 weeks+6 weeks). (B) Relevance of annotation in each data.

Figure 3—figure supplement 2
Analysis of 6-week snRNA-seq.

(A) Uniform manifold approximation and projection (UMAP) snRNA-seq clustering of cells harvested from 6-week mouse Achilles tendons. Annotation was based on each gene expression (ground-truth annotation, left) and predicted annotation inferred from 2-week snRNA-seq (right). (B) Identification of matching cell clusters between the 2-week and 6-week snRNA-seq data visualized as a heatmap. (C) Violin plot of tenocytes and tendon stem/progenitor cell (TSPC)-related gene expression in each cluster.

Figure 3—figure supplement 3
Comparison of 2-week and 6-week snATAC-seq.

(A) Circle plot of annotated differentially accessible regions for each data. (B) Integrated uniform manifold approximation and projection (UMAP) snATAC-seq clustering of cells harvested from 2-week and 6-week mouse Achilles tendons. (C) Feature plot of tendon stem/progenitor cell (TSPC)-related gene activity in each dataset.

Transcription factor landscapes of 2-week mouse Achilles tendons.

Single-Cell Regulatory Network Inference and Clustering (SCENIC) analysis of transcription factor activity based on 2-week snRNA-seq data for tenocytes and the tendon stem/progenitor cell (TSPC) lineage (left). Validation was performed based on the gene activity and motif activity of 2-week snATAC-seq and gene expression of 2-week snRNA-seq (right).

Figure 5 with 2 supplements
In vitro analysis of CD55+/CD248+ tendon stem/progenitor cells (TSPCs).

(A) Immunohistochemical image of 10-week mouse Achilles tendons. Scale bars show 100 µm. CD55 and CD248, green; Hoechst 33342, blue. (B) Schema of the in vitro assessment of the capacity of CD55+/CD248+ TSPCs as the differentiation toward tenocytes. (C) Colony-forming efficiency of CD55+/CD248+ and CD55-/CD248- (negative) TSPCs. Colonies were stained with crystal violet (n=6). CD55+/CD248+ TSPC exhibited higher clonogenic capacity. Data are presented as means ± scanning electron microscopy (SEM). **p<0.01. (D) Morphological changes of CD55+/CD248+ and negative TSPCs after tenogenic induction. (E) Quantitative PCR of tendon-related gene expression in CD55+/CD248+ and negative TSPCs after tenogenic induction (n=3). Data are presented as means ± SD. **p<0.01, *p<0.05. (F) SEM and transmission electron microscopy (TEM) imaging of artificial tendons derived from CD55+/CD248+ and negative TSPCs. Data are presented as means ± SD. **p<0.01, *p<0.05. (G) Proportions of fiber alignment for each artificial tendon (n=4). Data are presented as means ± SEM. ***p<0.005, **p<0.01, *p<0.05. (H) Diameter of collagen fiber in each artificial tendon based on TEM imaging (n=4). Data are presented as means ± SD. ***p<0.005. (I) Tensile strength (MPa) of each artificial tendon (n=5). Data are presented as means ± SEM. ***p<0.005.

Figure 5—figure supplement 1
Gene expression changes in CD55+/CD248+ and negative tendon stem/progenitor cells (TSPCs).

Quantitative PCR of gene expression in CD55+/CD248+ and negative TSPCs (n=4). Data are presented as means ± scanning electron microscopy (SEM). *p<0.05, ***p<0.005.

Figure 5—figure supplement 2
Chondrogenic and osteogenic induction of CD55+/CD248+ and negative tendon stem/progenitor cells (TSPCs).

Quantitative PCR of tendon-related genes in CD55+/CD248+ and negative TSPCs after chondrogenic and osteogenic induction (n=4). Data are presented as means ± scanning electron microscopy (SEM). **p<0.01, *p<0.05.

Tables

Table 1
Estimated transcription factor (TF) activity in each gene.
Estimated TF activity: Cd55
TFSpearman correlation
Klf40.264195541
Klf30.262413411
Zeb10.219593135
Pbx10.204085218
Hic10.202481054
Klf20.196232716
Nfe2l20.196076187
Estimated TF activity: Cd248
TFSpearman correlation
Hic10.375565336
Klf30.277768834
Zmiz10.272991765
Klf40.260526766
Zeb10.250583629
Sp30.2502976
Kdm5b0.193229132
Estimated TF activity: Mkx
TFSpearman correlation
Creb3l10.320638653
Zfhx30.169341424
Mxi10.149048856
Bhlhe400.144301452
Ets20.137445497
Max0.116134957
Elk30.098325126
Estimated TF activity: Scx
TFSpearman correlation
Creb3l10.316522613
Npdc10.163452737
Ets20.145463784
Mix10.121248221
Bhlhe410.115930755
Elk30.10803805
Bmyc0.104968457

Additional files

Supplementary file 1

Diferentially expressed genes in cluster 0, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp1-v1.csv
Supplementary file 2

Diferentially expressed genes in cluster 1, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp2-v1.csv
Supplementary file 3

Diferentially expressed genes in cluster 2, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp3-v1.csv
Supplementary file 4

Differentially expressed genes in cluster 3, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp4-v1.csv
Supplementary file 5

Differentially expressed genes in cluster 4, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp5-v1.csv
Supplementary file 6

Differentially expressed genes in cluster 5, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp6-v1.csv
Supplementary file 7

Differentially expressed genes in cluster 6, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp7-v1.csv
Supplementary file 8

Differentially expressed genes in cluster 7, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp8-v1.csv
Supplementary file 9

Differentially expressed genes in cluster 8, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp9-v1.csv
Supplementary file 10

Differentially expressed genes in cluster 9, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp10-v1.csv
Supplementary file 11

Differentially expressed genes in cluster 10, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp11-v1.csv
Supplementary file 12

Differentially expressed genes in cluster 11, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp12-v1.csv
Supplementary file 13

Differentially expressed genes in cluster 12, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp13-v1.csv
Supplementary file 14

Differentially expressed genes in cluster 13, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp14-v1.csv
Supplementary file 15

Differentially expressed genes in cluster 14, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp15-v1.csv
Supplementary file 16

Differentially expressed genes in cluster 15, related to Figure 1A.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp16-v1.csv
Supplementary file 17

PCR primers used in this study.

https://cdn.elifesciences.org/articles/104768/elife-104768-supp17-v1.xlsx
MDAR checklist
https://cdn.elifesciences.org/articles/104768/elife-104768-mdarchecklist1-v1.docx

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Hiroki Tsutsumi
  2. Tomoki Chiba
  3. Yuta Fujii
  4. Takahide Matsushima
  5. Tsuyoshi Kimura
  6. Akinori Kanai
  7. Akio Kishida
  8. Yutaka Suzuki
  9. Hiroshi Asahara
(2026)
Single-nucleus transcriptional and chromatin accessibility analyses of maturing mouse Achilles tendon uncover the molecular landscape of tendon stem/progenitor cells
eLife 14:RP104768.
https://doi.org/10.7554/eLife.104768.3