Standard
Active
Last Updated: Dec 23, 2024
Track Document
ASTM F2998-24
Standard Guide for Using Fluorescence Microscopy to Quantify the Spread Area of Fixed Cells
Standard Guide for Using Fluorescence Microscopy to Quantify the Spread Area of Fixed Cells
F2998-24
ASTM|F2998-24|en-US
Standard Guide for Using Fluorescence Microscopy to Quantify the Spread Area of Fixed Cells
Standard
F2998 Standard Guide for Using Fluorescence Microscopy to Quantify the Spread Area of Fixed Cells>
new
BOS Vol. 13.02 Committee F04
$
69.00
In stock
ASTM International
Significance and Use
4.1 Under well-controlled conditions, the quantitative evaluation of morphological features of a cell population can be used to identify changes in cellular behavior or state. Cell morphology changes may be expected when, for example, there is a response to changes in cellular cytoskeleton organization (1),2 a response of cells to toxic compounds, changes in differentiation state, and changes in adhesion properties of cells to a substrate by either chemical or mechanical-induced extracellular matrix-based (ECM-based) signaling pathways (2, 3). Typically, populations of cells exhibit a range of morphologies even when the cells are genetically identical and are in a homogeneous environment (4). This biological variation in cell response is due to both cell-cycle variations and stochasticity in the cellular reactions that control adhesion and spreading in cells. By using cell-by-cell, microscopy-based measurements and appropriate statistical sampling procedures, the distribution of cell morphologies such as cell spreading area per cell can be measured. This distribution is highly characteristic of the culture and conditions being examined.
4.2 It is important to note that the use of this technique for cells on or in a 3D scaffold material can complicate the interpretation of the data. The topographic transforms of the cells on a 3D material may require full volumetric imaging and not just wide-field fluorescence imaging as described here.
4.3 The following are several examples of how this measurement can be used in a laboratory:
4.3.1 Quantify Cellular Response to a Biomaterial—The measurement of cell spread area can be used to characterize the response of cells to biomaterials. For example, spreading of most cell types is extremely sensitive to the stiffness of the culture substrate (5, 6). It is important to note that cell response to an ECM may be dependent on the preparation of the matrix. For example, the same ECM proteins prepared in a fibrillar or non-fibrillar surface coating can result in different morphology response.
4.3.2 Quality Control Metric for General Cell Culture Conditions—Cell spread area may be a useful metric for monitoring a change in cell culture conditions (that is, due to a serum component, pH, passage number, confluence, etc.). Cell morphology is often altered when cells are stressed and proceeding through cell-death related processes (that is, apotoposis).
4.3.3 Quality Control Metric for Biomaterial Fabrication—Cell spread area measurements may be useful for generating specifications for a biomaterial. These specifications may stipulate how a particular cell line responds to a fabricated biomaterial.
4.3.4 Quality Control Metric for Cell Line Integrity and Morphology Benchmarking—The morphology characteristic of a cell line grown under specified conditions should ideally be the same over time and in different laboratories. Thus, cell spread area measurements may be useful for validating that no significant changes in the cell cultures have occurred. This measurement provides a benchmark that is useful for establishing the current state of the cell culture and a metric that can be charted to increased confidence for within and between laboratory comparisons of cellular measurements (7).
4.3.5 High Quality Training Data for Cell Morphology Image Analysis by Machine Learning (ML) Algorithms—The high-contrast staining practices described in this guide are designed to increase contrast during image collection and reduce variability in automated object edge detection algorithms. This can facilitate the generation of large data sets that can be used to train pattern recognition ML algorithms for the detection of specific cellular and non-cellular features. For example, the fluorescent whole-cell morphology and nuclei images can be used to train a machine learning algorithm to identify cell and non-cell pixels in non-stained transmission phase microscopy images. Fluorescent imaging settings such as exposure time, filters, pixel binning, and focus need to be considered to ensure image collection is appropriate for an ML algorithm training data (8).
Scope
1.1 This guide describes several measurement and technical issues involved in quantifying the spread area of fixed cells. Cell spreading and the distribution of cell spread areas of a population of cells are the result of a biological response that is dependent on intracellular signaling mechanisms and the characteristics of cell adhesion to a surface. Cell spread area is a morphological feature that can be responsive to alteration in the metabolic state or the state of stress of the cells. Changes in cell spread area can also indicate an alteration in the adhesion substrate that may be due to differences in manufacturing of the substrate material or in response to extracellular matrix secretions. High-quality measurement of cell spread area can serve as a useful metric for benchmarking and detecting changes in cell behavior under experimental conditions.
1.2 The measurement described in this guide is based on the use of microscopy imaging of fixed fluorescent cells and the use of image analysis algorithms to extract morphological data from the images. To produce robust cell spread area measurements, technical details involved in sample preparation, cell staining, microscopy imaging, image analysis, and statistical analysis should be considered. Several of these issues are discussed within this guide.
1.3 This standard is meant to serve as a guide for developing methods to reliably measure the area to which cells spread at a surface. This surface can be conventional tissue culture polystyrene or sophisticated engineered biomaterial surfaces. An example of a detailed procedure to measure the spreading area of cells on a tissue culture polystyrene surface is provided in the appendixes.
1.4 Cell morphology features such as cell spreading area and perimeter are generally reported in units of length. For example, spreading area per cell (that is, cell spread area) is likely reported in units of µm2. A spatial calibration standard is required to convert between numbers of pixels in a digital camera image to µm2 as an SI unit.
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.6 Sodium azide is used as a antibacterial reagent in the slide mounting media. This preserves the integrity of the mounting media. The toxicity of this reagent (for example, MSDS) should be considered before use of this reagent in large scale slide mounting procedures.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.