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软骨细胞的起源和命运:生理环境下的细胞可塑性。

The Origin and Fate of Chondrocytes: Cell Plasticity in Physiological Setting.

机构信息

Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Centre for Bone and Arthritis Research at the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Department of Physiology and Pharmacology, Karolinska Institute, Stockholm, Sweden.

出版信息

Curr Osteoporos Rep. 2023 Dec;21(6):815-824. doi: 10.1007/s11914-023-00827-1. Epub 2023 Oct 14.

DOI:10.1007/s11914-023-00827-1
PMID:37837512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10724094/
Abstract

PURPOSE OF REVIEW

Here, we discuss the origin of chondrocytes, their destiny, and their plasticity in relationship to bone growth, articulation, and formation of the trabeculae. We also consider these processes from a biological, clinical, and evolutionary perspective.

RECENT FINDINGS

Chondrocytes, which provide the template for the formation of most bones, are responsible for skeletal growth and articulation during postnatal life. In recent years our understanding of the fate of these cells has changed dramatically. Current evidence indicates a paradoxical situation during skeletogenesis, with some cells of mesenchymal condensation differentiating directly into osteoblasts, whereas others of the same kind give rise to highly similar osteoblasts via a complex process of differentiation involving several chondrocyte intermediates. The situation becomes even more paradoxical during postnatal growth when stem cells in the growth plate produce differentiated, functional progenies, which thereafter presumably dedifferentiate into another type of stem cell. Such a remarkable transition from one cell type to another under postnatal physiological conditions provides a fascinating example of cellular plasticity that may have valuable clinical implications.

摘要

目的综述

本文讨论了软骨细胞的起源、命运及其在骨骼生长、关节形成和小梁形成过程中的可塑性。我们还从生物学、临床和进化的角度来考虑这些过程。

最近的发现

软骨细胞为大多数骨骼的形成提供了模板,在出生后负责骨骼的生长和关节的活动。近年来,我们对这些细胞命运的认识发生了巨大的变化。目前的证据表明,在骨骼发生过程中存在一种矛盾的情况,一些间充质凝聚细胞直接分化为成骨细胞,而另一些相同类型的细胞通过涉及几个软骨细胞中间产物的复杂分化过程产生高度相似的成骨细胞。在出生后生长过程中,情况变得更加矛盾,生长板中的干细胞产生分化的、有功能的后代,此后这些细胞可能分化为另一种类型的干细胞。在出生后生理条件下,从一种细胞类型到另一种细胞类型的这种显著转变为细胞可塑性提供了一个引人入胜的例子,这可能具有重要的临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/10724094/fdaaaf582696/11914_2023_827_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/10724094/3743b27e2814/11914_2023_827_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/10724094/27224e59b74c/11914_2023_827_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/10724094/fdaaaf582696/11914_2023_827_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/10724094/3743b27e2814/11914_2023_827_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/10724094/27224e59b74c/11914_2023_827_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/10724094/fdaaaf582696/11914_2023_827_Fig3_HTML.jpg

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2
Notch Signaling Regulates the Chondrogenic Potential of Both Articular Chondrocytes and Their Progenitors During Expansion.Notch 信号在扩增过程中调节关节软骨细胞及其祖细胞的成软骨潜能。
Stem Cells. 2023 Jun 15;41(6):658-671. doi: 10.1093/stmcls/sxad031.
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MMP14 cleaves PTH1R in the chondrocyte-derived osteoblast lineage, curbing signaling intensity for proper bone anabolism.
JCI Insight. 2024 Feb 13;9(6):e165226. doi: 10.1172/jci.insight.165226.
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Complex Spatio-Temporal Interplay of Distinct Immune and Bone Cell Subsets during Bone Fracture Healing.复杂的时空相互作用:骨愈合过程中不同免疫细胞亚群和骨细胞亚群的作用。
Cells. 2023 Dec 24;13(1):40. doi: 10.3390/cells13010040.
MMP14 在软骨细胞衍生的成骨细胞谱系中裂解 PTH1R,抑制信号强度以实现适当的骨合成代谢。
Elife. 2023 Mar 9;12:e82142. doi: 10.7554/eLife.82142.
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Effects of temperature on metamorphosis and endochondral ossification in Rana chensinensis tadpoles.温度对中华蟾蜍蝌蚪变态和软骨内骨化的影响。
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