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

The 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 spa...

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Autores principales: Zhou, Taifeng, Chen, Yu, Liao, Zhiheng, Zhang, Long, Su, Deying, Li, Zhuling, Yang, Xiaoming, Ke, Xiaona, Liu, Hengyu, Chen, Yuyu, Weng, Ricong, Shen, Huimin, Xu, Caixia, Wan, Yong, Xu, Ren, Su, Peiqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10190614/
https://www.ncbi.nlm.nih.gov/pubmed/36965031
http://dx.doi.org/10.1002/advs.202206296
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author Zhou, Taifeng
Chen, Yu
Liao, Zhiheng
Zhang, Long
Su, Deying
Li, Zhuling
Yang, Xiaoming
Ke, Xiaona
Liu, Hengyu
Chen, Yuyu
Weng, Ricong
Shen, Huimin
Xu, Caixia
Wan, Yong
Xu, Ren
Su, Peiqiang
author_facet Zhou, Taifeng
Chen, Yu
Liao, Zhiheng
Zhang, Long
Su, Deying
Li, Zhuling
Yang, Xiaoming
Ke, Xiaona
Liu, Hengyu
Chen, Yuyu
Weng, Ricong
Shen, Huimin
Xu, Caixia
Wan, Yong
Xu, Ren
Su, Peiqiang
author_sort Zhou, Taifeng
collection PubMed
description The 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.
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spelling pubmed-101906142023-05-18 Spatiotemporal Characterization of Human Early Intervertebral Disc Formation at Single‐Cell Resolution Zhou, Taifeng Chen, Yu Liao, Zhiheng Zhang, Long Su, Deying Li, Zhuling Yang, Xiaoming Ke, Xiaona Liu, Hengyu Chen, Yuyu Weng, Ricong Shen, Huimin Xu, Caixia Wan, Yong Xu, Ren Su, Peiqiang Adv Sci (Weinh) Research Articles The 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. John Wiley and Sons Inc. 2023-03-25 /pmc/articles/PMC10190614/ /pubmed/36965031 http://dx.doi.org/10.1002/advs.202206296 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhou, Taifeng
Chen, Yu
Liao, Zhiheng
Zhang, Long
Su, Deying
Li, Zhuling
Yang, Xiaoming
Ke, Xiaona
Liu, Hengyu
Chen, Yuyu
Weng, Ricong
Shen, Huimin
Xu, Caixia
Wan, Yong
Xu, Ren
Su, Peiqiang
Spatiotemporal Characterization of Human Early Intervertebral Disc Formation at Single‐Cell Resolution
title Spatiotemporal Characterization of Human Early Intervertebral Disc Formation at Single‐Cell Resolution
title_full Spatiotemporal Characterization of Human Early Intervertebral Disc Formation at Single‐Cell Resolution
title_fullStr Spatiotemporal Characterization of Human Early Intervertebral Disc Formation at Single‐Cell Resolution
title_full_unstemmed Spatiotemporal Characterization of Human Early Intervertebral Disc Formation at Single‐Cell Resolution
title_short Spatiotemporal Characterization of Human Early Intervertebral Disc Formation at Single‐Cell Resolution
title_sort spatiotemporal characterization of human early intervertebral disc formation at single‐cell resolution
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10190614/
https://www.ncbi.nlm.nih.gov/pubmed/36965031
http://dx.doi.org/10.1002/advs.202206296
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