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Three-dimensional Characterization of Interorganelle Contact Sites in Hepatocytes using Serial Section Electron Microscopy.
Chun Chung, Gary Hong; Gissen, Paul; Stefan, Christopher J; Burden, Jemima J.
Afiliación
  • Chun Chung GH; MRC Laboratory for Molecular Cell Biology, University College London.
  • Gissen P; MRC Laboratory for Molecular Cell Biology, University College London; NIHR Great Ormond Street Hospital Biomedical Research Centre, University College London.
  • Stefan CJ; MRC Laboratory for Molecular Cell Biology, University College London.
  • Burden JJ; MRC Laboratory for Molecular Cell Biology, University College London; j.burden@ucl.ac.uk.
J Vis Exp ; (184)2022 06 09.
Article en En | MEDLINE | ID: mdl-35758663
Transmission electron microscopy has been long considered to be the gold standard for the visualization of cellular ultrastructure. However, analysis is often limited to two dimensions, hampering the ability to fully describe the three-dimensional (3D) ultrastructure and functional relationship between organelles. Volume electron microscopy (vEM) describes a collection of techniques that enable the interrogation of cellular ultrastructure in 3D at mesoscale, microscale, and nanoscale resolutions. This protocol provides an accessible and robust method to acquire vEM data using serial section transmission EM (TEM) and covers the technical aspects of sample processing through to digital 3D reconstruction in a single, straightforward workflow. To demonstrate the usefulness of this technique, the 3D ultrastructural relationship between the endoplasmic reticulum and mitochondria and their contact sites in liver hepatocytes is presented. Interorganelle contacts serve vital roles in the transfer of ions, lipids, nutrients, and other small molecules between organelles. However, despite their initial discovery in hepatocytes, there is still much to learn about their physical features, dynamics, and functions. Interorganelle contacts can display a range of morphologies, varying in the proximity of the two organelles to one another (typically ~10-30 nm) and the extent of the contact site (from punctate contacts to larger 3D cisternal-like contacts). The examination of close contacts requires high-resolution imaging, and serial section TEM is well suited to visualize the 3D ultrastructural of interorganelle contacts during hepatocyte differentiation, as well as alterations in hepatocyte architecture associated with metabolic diseases.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Retículo Endoplásmico / Mitocondrias Idioma: En Revista: J Vis Exp Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Retículo Endoplásmico / Mitocondrias Idioma: En Revista: J Vis Exp Año: 2022 Tipo del documento: Article