Tissue Formation during Embryogenesis

Marcel Karperien, Bernard A. J. Roelen, Rob E. Poelmann, Adriana C. Gittenberger-de Groot, Beerend P. Hierck, Marco C. DeRuiter, Dies Meijer, Susan Gibbs

Research output: Chapter in Book/Report/Conference proceedingChapterAcademicpeer-review

5 Citations (Scopus)

Abstract

The formation of functional organs and tissues during embryonic development is a complex process involving multiple cell types derived from ectoderm, mesoderm, endoderm, and the neural crest. These cell types interact via diverse mechanisms. Examples of such mechanisms are direct cell-cell contacts and paracrine signaling by morphogenic gradients. Cell behavior during organogenesis is dynamic and is dependent on cell movements of a subset of cells. Other cells revert their phenotype by a process called epithelial-to-mesenchyme transition and may become migratory. To obtain functional organs, cells respond to environmental signals like pulsatile blood flow by activation of adaptive signaling mechanisms, which direct tissue architecture. The timely, proper dosing and sequential integration of all these elements during organogenesis specifies cell types and shapes the organ’s form and function in the embryo. Tissue engineering relies on reiteration of these developmental processes and aims to combine this knowledge with typical engineering disciplines to generate functional substitutes to replace lost or worn out tissue. This process is known as developmental (re)engineering.
Original languageEnglish
Title of host publicationTissue Engineering
Subtitle of host publicationSecond Edition
PublisherElsevier
Pages67-109
Number of pages43
ISBN (Electronic)9780124201453
ISBN (Print)9780124202108
DOIs
Publication statusPublished - 1 Jan 2015

Publication series

NameTissue Engineering

Keywords

  • Cell-cell contacts
  • Developmental (re)engineering
  • Embryonic stem cells
  • Environmental adaptation
  • Epithelial-to-mesenchyme transition
  • Germ layer (Mesoderm, Endoderm, Ectoderm, and Neural Crest)
  • Morphogenic gradients and paracrine signaling

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