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Recombinant Limb Assay as Organoid Model. | LitMetric

Recombinant Limb Assay as Organoid Model.

Front Cell Dev Biol

Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad Universitaria, Ciudad de México, México.

Published: April 2022

AI Article Synopsis

  • Organ formation starts when cells commit to one of the three germ layers during early embryogenesis, guided by specific gene transcription networks that dictate cell fate and organ development.
  • Organoids can be generated from various stem cells to model this process, resulting in smaller, functional organs that mimic their larger counterparts.
  • The study proposes using the recombinant limb (RL) assay system to develop skeletal elements in organoids, leveraging embryonic signals to enable the formation of complex skeletal structures from stem cells or progenitor cells for enhanced research.

Article Abstract

Organ formation initiates once cells become committed to one of the three embryonic germ layers. In the early stages of embryogenesis, different gene transcription networks regulate cell fate after each germ layer is established, thereby directing the formation of complex tissues and functional organs. These events can be modeled by creating organoids from induced pluripotent, embryonic, or adult stem cells to study organ formation. Under these conditions, the induced cells are guided down the developmental pathways as in embryonic development, resulting in an organ of a smaller size that possesses the essential functions of the organ of interest. Although organoids are widely studied, the formation of skeletal elements in an organoid model has not yet been possible. Therefore, we suggest that the formation of skeletal elements using the recombinant limb (RL) assay system can serve as an organoid model. RLs are formed from undissociated or dissociated-reaggregated undifferentiated mesodermal cells introduced into an ectodermal cover obtained from an early limb bud. Next, this filled ectoderm is grafted into the back of a donor chick embryo. Under these conditions, the cells can receive the nascent embryonic signals and develop complex skeletal elements. We propose that the formation of skeletal elements induced through the RL system may occur from stem cells or other types of progenitors, thus enabling the study of morphogenetic properties from these cells for the first time.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086426PMC
http://dx.doi.org/10.3389/fcell.2022.863140DOI Listing

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