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Updated: Jul 26, 2025

Pancreatic Tissue Dissection to Isolate Viable Single Cells
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Pancreatic Tissue Dissection to Isolate Viable Single Cells.

Oshri Yosefov-Levi1, Sharona Tornovsky1, Oren Parnas2

  • 1The Lautenberg Center for Immunology and Cancer Research, The Institute for Medical Research Israel-Canada, Faculty of Medicine, The Hebrew University of Jerusalem.

Journal of Visualized Experiments : Jove
|June 12, 2023
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Summary
This summary is machine-generated.

This study presents a novel two-step protocol for pancreatic tissue digestion, crucial for isolating intact pancreatic acinar cells. The method effectively preserves cell viability, addressing a key challenge in pancreatic research.

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Area of Science:

  • Gastroenterology
  • Cell Biology
  • Biochemistry

Background:

  • The pancreas has endocrine and exocrine functions, with the exocrine system comprising 90% of the organ.
  • Pancreatic acinar cells produce digestive enzymes that can degrade cellular components like RNA.
  • Standard tissue dissociation methods often yield fragile cells and release damaging enzymes, hindering research.

Purpose of the Study:

  • To develop an improved protocol for pancreatic tissue digestion.
  • To enhance the recovery of intact and viable pancreatic acinar cells.
  • To provide a method applicable to normal, pre-malignant, and tumor pancreatic tissues.

Main Methods:

  • A novel two-step protocol for pancreatic tissue digestion was developed.
  • The protocol aims to minimize cell damage and enzyme degradation during dissociation.
  • The method was tested on normal, pre-malignant, and tumor pancreatic samples.

Main Results:

  • The developed protocol successfully recovers intact and viable pancreatic acinar cells.
  • This method overcomes the challenge of cell fragility and enzyme activity in pancreatic tissue.
  • The protocol is effective across diverse pancreatic tissue types, including those with stromal and immune cells.

Conclusions:

  • The two-step protocol offers a significant improvement for pancreatic tissue processing.
  • It enables better isolation of viable pancreatic acinar cells for downstream research.
  • This method is valuable for studying various pancreatic conditions, including tumors.