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Fast and precise targeting of single tumor cells in vivo by multimodal correlative microscopy.
Karreman, Matthia A; Mercier, Luc; Schieber, Nicole L; Solecki, Gergely; Allio, Guillaume; Winkler, Frank; Ruthensteiner, Bernhard; Goetz, Jacky G; Schwab, Yannick.
Afiliación
  • Karreman MA; Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.
  • Mercier L; MN3T, Inserm U1109, Strasbourg 67200, France Université de Strasbourg, Strasbourg 67000, France LabEx Medalis, Université de Strasbourg, Strasbourg 67000, France Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg 67000, France.
  • Schieber NL; Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.
  • Solecki G; Department of Neurooncology, University Hospital Heidelberg, Heidelberg 69120, Germany Clinical Cooperation Unit Neurooncology, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany.
  • Allio G; MN3T, Inserm U1109, Strasbourg 67200, France Université de Strasbourg, Strasbourg 67000, France LabEx Medalis, Université de Strasbourg, Strasbourg 67000, France Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg 67000, France.
  • Winkler F; Department of Neurooncology, University Hospital Heidelberg, Heidelberg 69120, Germany Clinical Cooperation Unit Neurooncology, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany.
  • Ruthensteiner B; Evertebrata Varia, Zoologische Staatssammlung München, Munich 81247, Germany.
  • Goetz JG; MN3T, Inserm U1109, Strasbourg 67200, France Université de Strasbourg, Strasbourg 67000, France LabEx Medalis, Université de Strasbourg, Strasbourg 67000, France Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg 67000, France jacky.goetz@inserm.fr sch
  • Schwab Y; Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany jacky.goetz@inserm.fr schwab@embl.de.
J Cell Sci ; 129(2): 444-56, 2016 Jan 15.
Article en En | MEDLINE | ID: mdl-26659665
Intravital microscopy provides dynamic understanding of multiple cell biological processes, but its limited resolution has so far precluded structural analysis. Because it is difficult to capture rare and transient events, only a few attempts have been made to observe specific developmental and pathological processes in animal models using electron microscopy. The multimodal correlative approach that we propose here combines intravital microscopy, microscopic X-ray computed tomography and three-dimensional electron microscopy. It enables a rapid (c.a. 2 weeks) and accurate (<5 µm) correlation of functional imaging to ultrastructural analysis of single cells in a relevant context. We demonstrate the power of our approach by capturing single tumor cells in the vasculature of the cerebral cortex and in subcutaneous tumors, providing unique insights into metastatic events. Providing a significantly improved throughput, our workflow enables multiple sampling, a prerequisite for making correlative imaging a relevant tool to study cell biology in vivo. Owing to the versatility of this workflow, we envision broad applications in various fields of biological research, such as cancer or developmental biology.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Rastreo Celular Límite: Animals Idioma: En Revista: J Cell Sci Año: 2016 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Rastreo Celular Límite: Animals Idioma: En Revista: J Cell Sci Año: 2016 Tipo del documento: Article País de afiliación: Alemania