Primary Hepatocytes Isolation with TissueGrinder

Hepatocytes directly isolated from liver tissue show a functionality very similar in culture as in vivo. They have become the “gold standard” for metabolism, clearance, hepatoxicity and drug-drug interaction and a lot more. The development of various mouse models have increased the availability of tissue samples over the past two decades.

Isolating hepatocytes from liver tissue samples is either time-consuming, non-standardized, not scalable or accepting all drawbacks of enzymatic digestion. Or all of them together. This is all the more important because it also implies major limitations for a 2D or 3D culture.
Microscopy image showing hepatocytes after tissue dissociation with clearly visible single cells.
TissueGrinder Benchtop with Grinding Consumable and Software
Green double arrows symbolizing fast cell processing and lab automation.

With the FFX TissueGrinder, liver samples can now be dissociated into single cell suspensions within a matter of just a few minutes enzyme-free. It is therefore a superior new option for obtaining a high yield of premium viable cells maintaining surface markers.

Comparison of conventional enzymatic tissue dissociation workflow versus TissueGrinder automated enzyme-free single-cell isolation.

Advantages of Primary Hepatocyte Isolation Without Enzymes

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Due to the enzyme-free approach, processing time is significantly reduced and​

Light blue double arrow symbol pointing right, representing speed, forward motion, or process acceleration.

the properties of the hepatocytes are preserved,

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not to mention that some enzymatic methods do not yield hepatocytes at all

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The contamination of the sample is effectivly prevented by the integration of the grinding component together with a cell strainer into a centrifugation tube.​

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This improves the quality of any subsequent cell culture significantly.​

Applications of Primary Hepatocyte Isolation in Research

RT-DC scatterplot of cell size versus deformation comparing two runs of mechanically dissociated tissue using the TissueGrinder.

In a flow cytometry scatterplot, hepatocytes are easily visible, when the tissue sample is dissociated with the TissueGrinder.

RT-DC scatterplot showing cell deformation versus size for single-cell analysis, comparing two experimental runs.

In contrast, hepatocytes cannot be analyzed with enzymatic tissue dissociation.

The TissueGrinder gives a good yield of hepatocytes, while there are close to none retrievable from the enzymatic process.

The generated primary cells can be employed to create tissue models such as spheroids, micro tissues, organoids and cell printed systems. New cell lines can easily be established for molecular cell characterization and drug screenings.

enzymatic digestion

Microscopic image of hepatocytes after enzymatic digestion on Day 0, showing dispersed single cells and small clusters.

TissueGrinder dissociation

Microscopic image of hepatocytes after TissueGrinder dissociation on Day 0, showing dispersed single cells forming an early suspension.

Day 0

d0

Microscopic image of hepatocytes after enzymatic digestion on Day 1, showing a dense central cell cluster surrounded by dispersed single cells.
Microscopic image of hepatocytes after TissueGrinder dissociation on Day 1, showing a large central cluster with partially dissociated cells.

Day 1

d1

Close-up of TissueGrinder tube components with transparent grinding inserts and blue cap for tissue dissociation.
TissueGrinder benchtop device for automated mechanical tissue dissociation in laboratory workflows.
Hand holding a 50 ml centrifuge tube with blue cap and pink solution for tissue processing.

Sounds too good to be true?

Then contact us to arrange a test run with your own samples!