Monitoring Hypoxia (2024)

How is Hypoxia Detected?

While specialized machinery can directly control and measure levels of oxygen, methods to monitor hypoxia often rely on strategies for the detection of HIF protein expression and other hypoxia markers. Monitoring HIF-alpha levels within cells and tissues provides a measure of the extent of hypoxia and hypoxic gradients. Because HIFs have a notoriously short half-life and are extremely sensitive to oxygen levels, hypoxia is also monitored by key proteins regulated by HIFs (e.g., CA IX, VEGF). Other strategies to detect and monitor hypoxia in vitro include monitoring changes in gene expression via in situ hybridization (ISH) or using fluorescent oxygen-sensitive dyes.Pimonidazole(Catalog # 6182) is commonly used to detect hypoxia in vivo.

Hypoxia Markers

Common Hypoxia Marker Antibodies

Under normoxic conditions,HIF-alphasubunits are rapidly targeted for degradation by the proteasomal system. Under hypoxia, HIF-alpha subunits are stable resulting in increased protein levels, particularly in the nucleus. Stabilization of HIF-alpha leads to increased expression of downstream proteins, adapting the cells to their hypoxic environment.

Find our top cited HIF-1 alpha antibody(NB100-105), with over900 citations.

In addition to observed changes in protein expression, hypoxia and the cellular stress response can be monitored by interrogating the function of mitochondria. Mitochondria are an important site of oxygen consumption within the cell, converting glucose into ATP via oxidative phosphorylation (OXPHOS). In addition to the cellular response to hypoxia, mitochondria are critically important in the cellular stress response pathways ofautophagyandapoptosis. Bio-Techne has antibodies to criticalmitochondrial markers, includingATP5A,NDUFC2andCOX4.

Mitochondrial function can also be assessed with variousfluorescent probesavailable through Bio-Techne brand, Tocris.

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Hypoxia Marker Detection in Cell Lysate

Detection and monitoring of hypoxia in cell lysate are important tools to understand the nature of the cellular environment on a population level. Techniques to detect and monitor hypoxia markers in cell lysate includewestern blotandELISA.

Bio-Techne offers instruments to automate and streamline western blot and ELISA workflows:

While useful for preliminary screening, these whole cell lysate or subcellular fraction analyses present an average of total protein expression in the sample. Cells are exposed to various degrees of hypoxia depending on their location within the microenvironment and differential cellular responses would only be visible by a more nuanced, single-cell approach.

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Single-Cell Detection of Hypoxia

Detection of hypoxia at the single-cell level can provide important information about the individual cellular response to hypoxia and how cells respond to the hypoxic gradient within cultures and tissues. In general, these techniques allow for more phenotypic information from one sample and show heterogeneity within cell cultures and tissue samples. Some common techniques to analyze hypoxia at single-cell level includeflow cytometry,mass cytometry,ICC,IHC,ISH, and imaging cytometry.

Additional techniques include imaging cytometry and imaging mass cytometry, combining the single-cell resolution and high throughput nature of conventional cytometry with the spatial data acquired with imaging techniques.

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Hypoxia in 2D and 3D Culture Models

Hypoxia is common in tumors and occurs as the result of increased cell proliferation and metabolism, as well as deficiencies in blood supply and reduced tissue-oxygen diffusion. These factors continually expose tumor cells to fluctuating oxygenation which is difficult to replicate in the laboratory setting.

2D cell culture model systems have been predominantly used to study hypoxic responses. Most studies rely on culturing hom*ogeneous cancer cell lines on flat surfaces that do not replicate the biologically significant extracellular environment.

Additional limitations of monolayer cell cultures include:

• Cell-cell interactions are unlike those foundin vivo
• Cells acquire abnormal morphology
• Cells have atypical distribution of membrane proteins

Various studies have shown that signaling pathways activated and resulting cellular adaptations that occur under hypoxia are influenced by the way cells are cultured in vitro. Therefore, 3D spheroid cell cultures have progressively become more accepted as model systems that more faithfully replicate the tumor microenvironment.

HIFs are stabilized in spheroids according to graded oxygen levels, similar to hypoxic tumor regions, reaching maximal expression in cells peripheral to the core. Several types of 3D spherical cultures have been developed that are reviewed in the white paper,A Technical Perspective: Understanding the Cellular Response to Hypoxia through In Vitro Model Systems

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