Cellular Heterogeneity and Lineage Restriction during Mouse Digit Tip Regeneration at Single-Cell Resolution

被引:58
|
作者
Johnson, Gemma L. [1 ,2 ]
Masias, Erick J. [1 ]
Lehoczky, Jessica A. [1 ]
机构
[1] Brigham & Womens Hosp, Dept Orthoped Surg, Boston, MA 02115 USA
[2] Harvard Med Sch, Dept Syst Biol, Boston, MA 02115 USA
关键词
LIMB REGENERATION; IMPRINTED GENE; GROWTH; ANGIOGENESIS; EXPRESSION; ORIGIN; PROLIFERATION; MACROPHAGES; BEHAVIOR; TENDONS;
D O I
10.1016/j.devcel.2020.01.026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Innate regeneration following digit tip amputation is one of the few examples of epimorphic regeneration in mammals. Digit tip regeneration is mediated by the blastema, the same structure invoked during limb regeneration in some lower vertebrates. By genetic lineage analyses, the digit tip blastema has been defined as a population of heterogeneous, lineage-restricted progenitor cells. These previous studies, however, do not comprehensively evaluate blastema heterogeneity or address lineage restriction of closely related cell types. In this report, we present single-cell RNA sequencing of over 38,000 cells from mouse digit tip blastemas and unamputated control digit tips and generate an atlas of the cell types participating in digit tip regeneration. We computationally define differentiation trajectories of vascular, monocytic, and fibroblastic lineages over regeneration, and while our data confirm broad lineage restriction of progenitors, our analysis reveals 67 genes enriched in blastema fibroblasts including a novel regeneration-specific gene, Mest.
引用
收藏
页码:525 / +
页数:21
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