How a Flow Cytometer Works

Topics in this section:

• Statistical power to analyze millions of cells
• Potential applications for flow cytometry
• Overview of how a flow cytometer works
• Summary

Introduction to flow cytometry

Flow cytometry is a cell analysis technique that was first used in the 1950s to measure the volume of cells in a rapidly flowing fluid stream as they passed in front of a viewing aperture. Since that time, innovations from many engineers and researchers have culminated in the modern flow cytometer, which is able to make measurements of cells in solution as they pass by the instrument’s laser at rates of 10,000 cells per second (or more). Today’s instruments offer an increased number of detectable fluorescent parameters (from 1 or 2 up to ~30 or more), all measured at the same time on the same cell. Because of its speed and ability to scrutinize at the single-cell level, flow cytometry offers the cell biologist the statistical power to rapidly analyze and characterize millions of cells, albeit at the expense of the morphological characteristics and subcellular localization that microscopy can provide. Science, like the rest of life, is all about trade-offs! See Table 1 for a comparison of flow cytometry and microscopy techniques.

Table 1. Comparing flow cytometry and fluorescence imaging microscopy as techniques for cellular analysis.

Potential applications for flow cytometry

The potential applications of analysis by flow cytometry are numerous, including the detection and measurement of:

• Protein expression—throughout the entire cell, even the nucleus
• Protein post translational modifications—includes cleaved and phosphorylated proteins
• RNA—including IncRNA, miRNA, and mRNA transcripts
• Cell health status—from viability to late-stage apoptosis or programmed cell death
• Cell cycle status—providing a powerful tool to assess cells in G0/G1 phase versus S phase, G2, or polyploidy, including analysis of cell proliferation and activation
• Identification and characterization of distinct subsets of cells within a heterogeneous sample—including distinguishing central effector memory cells from exhausted T cells or even regulatory T cells

An additional capability of specialized flow cytometers is the ability to sort cells and recover the subsets for post experimental use. This specialized flow cytometer is called a fluorescence activated cell sorter (FACS), a term that is sometimes erroneously used interchangeably with ‘flow cytometer’. This usage is incorrect. A flow cytometer is an analytical machine that does not perform cell sorting. Cell sorters use fluidics and fluorescence components similar to those in flow cytometers, but are able to divert a specific population from within a heterogeneous sample into a separate tube, typically based on specified fluorescence characteristics. If collected under sterile conditions, these cells can be further cultured, manipulated, and studied.

Overview of how a flow cytometer works

The three main components of a flow cytometer are the fluidics, optics, and electronics (Figure 1).

• The fluidics system of a flow cytometer is responsible for transporting sample from the sample tube to the flow cell. Once through the flow cell (and past the laser), the sample is either sorted (in the case of cell sorters) or transported to waste.
• The components of the optical system include excitation light sources, lenses, and filters used to collect and move light around the instrument and the detection system that generates the photocurrent.
• The electronics are the brains of the flow cytometer. Here, the photocurrent from the detector is digitized and processed to be saved for subsequent analysis. 

Sample uptake into the instrument

A typical experiment begins with fluorescently labeled cells in a single-cell suspension, but a sample containing particles of any kind can be used. Once the sample is placed on the flow cytometer, the sample is taken up into the instrument, and the cells are surrounded by a physiological buffer called sheath fluid. The fluidics system—the tubing, pumps, and valves—organizes the initial sample suspension into a single-file stream of cells (Figure 2) as they make their journey through the flow cytometer for analysis.

Interrogation point

The place where the cells interact with laser light is called the interrogation point (Figure 3). You might also hear it referred to as the laser intercept. This is where the action takes place. When the laser light beam illuminates a single cell, some of the light will strike physical structures within the cell, causing the light to scatter. This light scatter can be measured and correlated with relative cell size and structures inside the cell. These measurements are termed forward angle scatter(FSC) and side angle scatter (SSC), depending on where the light is collected with respect to the path of the laser. Nearly simultaneously, light from the laser will excite all fluorophores associated with the cell, which produces a fluorescence emission. All of this light is collected by the detector and processed through the electronics component of the flow cytometer. After passing through the interrogation point, the cell is no longer needed and is carried by the fluidics system to the waste container. If this were a cell sorter, this would be the point where the cell would be passed to a collection tube and used for further experiments.

Summary

Flow cytometry is a powerful tool that can be used in a significant number of cell analysis applications ranging from phenotyping to cell health and viability.

The two greatest advantages of flow cytometry are its ability to measure a large number of parameters (2 to 30 or more) on the same sample and its ability to collect information from millions of cells in a matter of seconds.

There are 3 main components of a flow cytometer—the fluidics, optics and electronics—that work together to provide a complete system of cell analysis (Figure 4).