Cellometer Vision Application:

Development of a Novel Method to Assess Primary Hepatocyte Concentration and Viability

Schedule an Online Demo

Download PDF

Introduction

Brightfield image of primary human
hepotocytes. Live and dead
hepatocytes show different
morphology but are difficult to clearly
distinguish resulting in counting
variability.

After treating samples with
Fluorescence Dual Staining Solution,
AO stained live hepatocytes and PI
stained dead/dying hepatocytes are
easily distinguished in this
fluorescence image.

Cellometer Vision incorporates image based cell counting and fluorescence detection in a compact and easy-to-use instrument. With dual fluorescence detection capabilities, Cellometer Vision is an ideal solution for many complex cell population characterization assays such as reliably counting and determining viability of primary hepatocytes.

Reliable concentration and viability data of primary Hepatocytes is critical for accurate analysis of compound toxicity in vitro. Due to hepatocytes' variable morphology, fragile nature and tendency to clump, traditional manual counting methods are time consuming and the subjectivity from operator-to-operator can cause inconsistent results.

Nexcelom's new method incorporates staining primary hepatocytes with a ready-to-use fluorescent dual staining solution that stains live cells with acridine orange, and dead cells with propidium iodide and then loading 20µL of labled sample into a disposable counting chamber for analysis. Since the counting chamber is disposable, no washing is required between samples, and the risk of cross contamination is eliminated.

Fluorescent images of the stained cells are captured and using proprietary algorithms, Cellometer Vision's robust operating software accurately analyzes cell images to generate live cell count, concentration & viability percentage. Total analysis time typically takes less than 60 seconds. Cell images and all analysis data, including cell size distribution histograms, can be instantly saved for documentation. Data can also be easily exported to Microsoft Excel spreadsheets for further analysis.

Cellometer Vision automatically analyzes fluorescent images of dual stained
hepatocytes and instantly calculates live cell concentration and viability.

Method

Treat cell sample with Nexcelom's Fluorescence Dual Staining Solution:

Take 20µl of freshly isolated hepatocyte sample or freeze-thaw cryopreserved cell sample in a small microtube.
Apply 20µl of ready-to-use dual staining solution (acridine orange/propidium iodide cocktail).
Gently mix. Sample is ready to count.

Running Assay:

Load 20µl of labeled sample into the Cellometer disposable counting chamber.
Insert counting chamber into Cellometer Vision.
Select assay from drop-down menu & enter Sample ID.
Preview cell images and click 'Count' to begin analyzing sample.
Review Images and counting results.
Save or Export images and/or report data.

Results

AO stained live hepatocytes are clearly visible in the fluorescence image obtained from Filter Set 101 (Figure 1). The software indicates counted cells with a green circle (enlarged to show detail) while ignoring cellular debris. The software also can recognize and discretely count clumpy cells. PI stained dead cells are visible in the image obtained Figure 1. The fluorescent image from Filter Set 101(R) shows counted AO stained live hepatocytes. Cellular debris seen in the brightfield image (L) are not counted in the fluorescence image. Figure 2. The fluorescent image (R) from Filter Set 202 shows counted PI stained dead hepatocytes (Circled with green). Free from Filter Set 202 (Figure 2). The software then accurately calculates total cell count, concentration and viability (below). By using this method, live and dead cells are clearly distinguished and automatically counted for improved accuracy. By combining a ready to use staining solution and imaging based system results can be obtained much easier and faster compared to other methods.

Counting results are displayed on-screen instantly. Fluorescent 1 indicates AO stained live cells, Fluorescent 2 indicates PI stained dead cells. Viability percentage is calculated automatically. Results can be saved to a data table (below)

Sample ID	Image	Cell counts	Dilution factor	Concentration (cell/ml)	Viability	Mean diameter (mm)
Rat fresh hepatocyte	F1 live F1 dead	738 137	2 2	2.1E+06 3.9E+05	84.3%	19.3
Rat feash diluted	F1 live F1 dead	405 98	2 2	1.2E+06 2.8E+05	80.5%	21.0
Dog cryopreserved	F1 live F1 dead	352 162	2 2	1.0E+06 4.5E+05	68.5%	16.4
Mouse cryopreserved	F1 live F1 dead	163 295	2 2	4.7E+05 8.4E+05	35.6%	19.3

Figure 1. The fluorescent image from Filter Set 101(R) shows counted AO stained live
hepatocytes. Cellular debris seen in the brighttield image (L) are not counted in the
fluorescence image.

Figure 2. The fluorescent image (R) from Filter Set 202 shows counted PI stained dead
hepatocytes (Circled with green). Free nuclei from lysed dead cells are not counted.

Figure 3. By overlaying AO/live and PI/dead hepatocyte images, counting results can
be visually confirmed. Live hepatocytes are circled in green and dead hepatocytes
circled in orange (R)..

Schedule an Online Demo

Download PDF

CELLOMETER Vision Trio SPECIFICATIONS:

Imaging Modes: Brightfield & 2 Fluorescence Channels
Filter Set 101: Excitation/Emission Peak: 475nm/535nm
Flter Set 202: Excitation/Emission Peak: 525nm /595nm
Dimensions: 6"x 8.5" x 14" (15cm x 22cm x 36cm)
Weight: 25lbs (11kg)
PC Specs: WinXP/1.8+GHz/1GB RAM/laptop included

Other Cellometer Vision Applications:

Quantifying GFP Transfection
Counting WBCs in Whole Blood without Lysing
Annexin-V for Detection of Apoptosis
Determination of Cell Viability with Propidium Iodide
Counting and Sizing Adipocytes
Counting & Calculating Viability of Hepatocytes
Determining Yeast Viability
Counting and Determining Viability of Stem cells

Join our free webinar. "Improving Cell Counting Data Quality & Throughput" on Friday, March 19, 2010 @ 10:00am EDT. Register now