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Centre de Recherche en Cancérologie de Lyon

3 ARTICLES PUBLISHED IN JoVE

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Biology

Isolation and Culture of Mouse Primary Pancreatic Acinar Cells
Johann Gout 1,2,3,4,5, Roxane M. Pommier 1,2,3,4,5, David F. Vincent 1,2,3,4,5, Bastien Kaniewski 1,2,3,4,5, Sylvie Martel 1,2,3,4,5, Ulrich Valcourt *1,2,3,4,5, Laurent Bartholin *1,2,3,4,5
1INSERM U1052, Centre de Recherche en Cancérologie de Lyon, 2CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, 3Université de Lyon, 4Université Lyon 1, 5Centre Léon Bérard

In this publication, we describe a rapid and convenient procedure for isolating and culturing primary pancreatic acinar cells from the murine pancreas. This method constitutes a valuable approach to study the physiology of fresh primary normal/untransformed exocrine pancreatic cells.

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Cancer Research

Proximity Ligation Assay Allows the Detection, Localization, and Quantification of Protein Arginine Methylation in Fixed Tissue
Coralie Poulard *1,2,3, Julien Jacquemetton *1,2,3, Julie Valantin 1,2,3,4,5, Isabelle Treilleux 1,2,3,4, Muriel Le Romancer 1,2,3
1Université de Lyon, 2Inserm U1052, Centre de Recherche en Cancérologie de Lyon, 3CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, 4Pathology Department, Centre Leon Bérard, 5Plateforme Anatomopathologie Recherche

Proximity ligation assay is a very useful technique to localize and quantify arginine methylation of a given protein when the modified arginine residue is unknown and/or if no specific antibody is available.

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Biology

A Human Bone Marrow 3D Model to Investigate the Dynamics and Interactions Between Resident Cells in Physiological or Tumoral Contexts
Kawtar Arizkane 1,2,3, Kevin Geistlich 1,2,3,4, Laurine Moindrot 1,2,3, Emma Risson 1,2,3, Sandrine Jeanpierre 1,2,3,4, Léa Barral 1,2,3, Anaëlle Bobard 1,2,3, Giulio Menegazzi 5, Thibault Voeltzel 1,2,3, Véronique Maguer-Satta 1,2,3, Sylvain Lefort 1,2,3
1Centre de Recherche en Cancérologie de Lyon, 2Centre de Recherche en Cancérologie de Lyon, 3Université de Lyon, 4Centre Léon Bérard, 5Department of Experimental and Clinical Biomedical Sciences Mario Serio, Università degli Studi di Firenze

Here, we describe an easy-to-implement, standardized, microphysiological system that reflects the complexity of the human bone marrow's in vivo structure, providing a pertinent model to finely study a broad range of normal and pathological events.

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