SWIP—a stabilized window for intravital imaging of the murine pancreas

Author:

Du Wei12,Adkisson Christian234,Ye Xianjun2567,Duran Camille L.257,Chellakkan Selvanesan Benson8,Gravekamp Claudia8,Oktay Maja H.257,McAuliffe John C.456,Condeelis John S.23456,Panarelli Nicole C.567,Norgard Robert J.9,Sela Yogev9,Stanger Ben Z.9,Entenberg David2567ORCID

Affiliation:

1. Breast Center, Peking University People's Hospital, Beijing, People's Republic of China

2. Anatomy and Structural Biology, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, USA

3. Department of Cell Biology, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, USA

4. Department of Surgery, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, USA

5. Gruss-Lipper Biophotonics Center, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, USA

6. Integrated Imaging Program, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, USA

7. Department of Pathology, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, USA

8. Department of Microbiology and Immunology, Einstein College of Medicine/Montefiore Medical Center, Bronx, NY, USA

9. Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

Abstract

Pancreatitis and pancreatic ductal adenocarcinoma (PDAC) are grave illnesses with high levels of morbidity and mortality. Intravital imaging (IVI) is a powerful technique for visualizing physiological processes in both health and disease. However, the application of IVI to the murine pancreas presents significant challenges, as it is a deep, compliant, visceral organ that is difficult to access, easily damaged and susceptible to motion artefacts. Existing imaging windows for stabilizing the pancreas during IVI have unfortunately shown poor stability for time-lapsed imaging on the minutes to hours scale, or are unable to accommodate both the healthy and tumour-bearing pancreata. To address these issues, we developed an improved stabilized window for intravital imaging of the pancreas (SWIP), which can be applied to not only the healthy pancreas but also to solid tumours like PDAC. Here, we validate the SWIP and use it to visualize a variety of processes for the first time, including (1) single-cell dynamics within the healthy pancreas, (2) transformation from healthy pancreas to acute pancreatitis induced by cerulein, and (3) the physiology of PDAC in both autochthonous and orthotopically injected models. SWIP can not only improve the imaging stability but also expand the application of IVI in both benign and malignant pancreas diseases.

Funder

Gruss-Lipper Biophotonics Center

National Institutes of Health

The EGL Charitable Foundation

Jane A. and Myles P. Dempsey

Integrated Imaging Program

Publisher

The Royal Society

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,General Neuroscience

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