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Intrinsic and growth-mediated cell and matrix specialization during murine meniscus tissue assembly
Journal article   Open access   Peer reviewed

Intrinsic and growth-mediated cell and matrix specialization during murine meniscus tissue assembly

Tonia K Tsinman, Xi Jiang, Lin Han, Eiki Koyama, Robert L Mauck and Nathaniel A Dyment
The FASEB journal, v 35(8), pp e21779-n/a
Aug 2021
PMID: 34314047
url
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8323983View
Accepted (AM)Open Access (License Unspecified) Open

Abstract

Animals Cartilage - embryology Cartilage - growth & development Cartilage - metabolism Cell Differentiation Cell Proliferation Collagen - metabolism Extracellular Matrix - metabolism Meniscus - embryology Meniscus - growth & development Meniscus - metabolism Mice Mice, Transgenic
The incredible mechanical strength and durability of mature fibrous tissues and their extremely limited turnover and regenerative capacity underscores the importance of proper matrix assembly during early postnatal growth. In tissues with composite extracellular matrix (ECM) structures, such as the adult knee meniscus, fibrous (Collagen-I rich), and cartilaginous (Collagen-II, proteoglycan-rich) matrix components are regionally segregated to the outer and inner portions of the tissue, respectively. While this spatial variation in composition is appreciated to be functionally important for resisting complex mechanical loads associated with gait, the establishment of these specialized zones is poorly understood. To address this issue, the following study tracked the growth of the murine meniscus from its embryonic formation through its first month of growth, encompassing the critical time-window during which animals begin to ambulate and weight bear. Using histological analysis, region specific high-throughput qPCR, and Col-1, and Col-2 fluorescent reporter mice, we found that matrix and cellular features defining specific tissue zones were already present at birth, before continuous weight-bearing had occurred. These differences in meniscus zones were further refined with postnatal growth and maturation, resulting in specialization of mature tissue regions. Taken together, this work establishes a detailed timeline of the concurrent spatiotemporal changes that occur at both the cellular and matrix level throughout meniscus maturation. The findings of this study provide a framework for investigating the reciprocal feedback between cells and their evolving microenvironments during assembly of a mechanically robust fibrocartilage tissue, thus providing insight into mechanisms of tissue degeneration and effective regenerative strategies.

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Collaboration types
Domestic collaboration
Web of Science research areas
Biochemistry & Molecular Biology
Biology
Cell Biology
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