Spatiotemporal Characterization of Human Early Intervertebral Disc Formation at Single‐Cell Resolution

Author:

Zhou Taifeng1,Chen Yu2,Liao Zhiheng1,Zhang Long2,Su Deying3,Li Zhuling1,Yang Xiaoming4,Ke Xiaona1,Liu Hengyu1,Chen Yuyu1,Weng Ricong1,Shen Huimin5,Xu Caixia6,Wan Yong1,Xu Ren2,Su Peiqiang1ORCID

Affiliation:

1. Department of Spine Surgery Guangdong Provincial Key Laboratory of Orthopedics and Traumatology The First Affiliated Hospital of Sun Yat‐sen University Guangzhou 510080 China

2. State Key Laboratory of Cellular Stress Biology Fujian Provincial Key Laboratory of Organ and Tissue Regeneration School of Medicine Faculty of Medicine and Life Sciences Xiamen University Xiamen 361102 China

3. Guangdong Provincial Key Laboratory of Proteomics and State Key Laboratory of Organ Failure Research School of Basic Medical Sciences Southern Medical University Guangzhou 510515 China

4. Department of Orthopedics Renmin Hospital of Wuhan University Wuhan 430060 China

5. Department of Gynecology and Obstetrics The First Affiliated Hospital of Sun Yat‐sen University Guangzhou 510080 China

6. Research Center for Translational Medicine The First Affiliated Hospital of Sun Yat‐sen University Guangzhou 510080 China

Abstract

AbstractThe intervertebral disc (IVD) acts as a fibrocartilaginous joint to anchor adjacent vertebrae. Although several studies have demonstrated the cellular heterogeneity of adult mature IVDs, a single‐cell transcriptomic atlas mapping early IVD formation is still lacking. Here, the authors generate a spatiotemporal and single cell‐based transcriptomic atlas of human IVD formation at the embryonic stage and a comparative mouse transcript landscape. They identify two novel human notochord (NC)/nucleus pulposus (NP) clusters, SRY‐box transcription factor 10 (SOX10)+ and cathepsin K (CTSK)+, that are distributed in the early and late stages of IVD formation and they are validated by lineage tracing experiments in mice. Matrisome NC/NP clusters, T‐box transcription factor T (TBXT)+ and CTSK+, are responsible for the extracellular matrix homeostasis. The IVD atlas suggests that a subcluster of the vertebral chondrocyte subcluster might give rise to an inner annulus fibrosus of chondrogenic origin, while the fibroblastic outer annulus fibrosus preferentially expresseds transgelin and fibromodulin . Through analyzing intercellular crosstalk, the authors further find that notochordal secreted phosphoprotein 1 (SPP1) is a novel cue in the IVD microenvironment, and it is associated with IVD development and degeneration. In conclusion, the single‐cell transcriptomic atlas will be leveraged to develop preventative and regenerative strategies for IVD degeneration.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Natural Science Foundation of Guangdong Province

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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