Micro-computed tomography as a platform for exploring development.

Development

Cell Biology and Physiology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA

Published: December 2019

AI Article Synopsis

  • Understanding the connection between molecular events and tissue function is crucial for exploring development and diseases in animals.
  • The study leverages model organisms and advanced technologies like micro-computed tomography (µ-CT) for non-invasive, high-resolution imaging of tissues at various developmental stages.
  • By using µ-CT to investigate brain growth defects linked to genes associated with microcephaly, the research highlights the effectiveness of combining imaging techniques with genetic and biological methods to explore mechanisms of development and disease.

Article Abstract

Understanding how events at the molecular and cellular scales contribute to tissue form and function is key to uncovering the mechanisms driving animal development, physiology and disease. Elucidating these mechanisms has been enhanced through the study of model organisms and the use of sophisticated genetic, biochemical and imaging tools. Here, we present an accessible method for non-invasive imaging of at high resolution using micro-computed tomography (µ-CT). We show how rapid processing of intact animals, at any developmental stage, provides precise quantitative assessment of tissue size and morphology, and permits analysis of inter-organ relationships. We then use µ-CT imaging to study growth defects in the brain through the characterization of () and (), orthologs of the two most commonly mutated genes in human microcephaly patients. Our work demonstrates the power of combining µ-CT with traditional genetic, cellular and developmental biology tools available in model organisms to address novel biological mechanisms that control animal development and disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918772PMC
http://dx.doi.org/10.1242/dev.176685DOI Listing

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