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Extracellular Matrix and Cellular Plasticity in Musculoskeletal Development.
Ma, Sophia Ka Yan; Chan, Andy Shing Fung; Rubab, Aqsa; Chan, Wilson Cheuk Wing; Chan, Danny.
Affiliation
  • Ma SKY; School of Biomedical Sciences, The University of Hong Kong, Hong Kong, China.
  • Chan ASF; School of Biomedical Sciences, The University of Hong Kong, Hong Kong, China.
  • Rubab A; School of Biomedical Sciences, The University of Hong Kong, Hong Kong, China.
  • Chan WCW; School of Biomedical Sciences, The University of Hong Kong, Hong Kong, China.
  • Chan D; Department of Orthopedics Surgery and Traumatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Front Cell Dev Biol ; 8: 781, 2020.
Article in En | MEDLINE | ID: mdl-32984311
ABSTRACT
Cellular plasticity refers to the ability of cell fates to be reprogrammed given the proper signals, allowing for dedifferentiation or transdifferentiation into different cell fates. In vitro, this can be induced through direct activation of gene expression, however this process does not naturally occur in vivo. Instead, the microenvironment consisting of the extracellular matrix (ECM) and signaling factors, directs the signals presented to cells. Often the ECM is involved in regulating both biochemical and mechanical signals. In stem cell populations, this niche is necessary for maintenance and proper function of the stem cell pool. However, recent studies have demonstrated that differentiated or lineage restricted cells can exit their current state and transform into another state under different situations during development and regeneration. This may be achieved through (1) cells responding to a changing niche; (2) cells migrating and encountering a new niche; and (3) formation of a transitional niche followed by restoration of the homeostatic niche to sequentially guide cells along the regenerative process. This review focuses on examples in musculoskeletal biology, with the concept of ECM regulating cells and stem cells in development and regeneration, extending beyond the conventional concept of small population of progenitor cells, but under the right circumstances even "lineage-restricted" or differentiated cells can be reprogrammed to enter into a different fate.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Cell Dev Biol Year: 2020 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Cell Dev Biol Year: 2020 Document type: Article Affiliation country: China
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