In Vivo Imaging

Learn about in vivo imaging techniques including bioluminescence and fluorescence imaging, advantages, challenges, and applications in research.

What is In Vivo Imaging?

In vivo imaging refers to a variety of techniques used to visualize and study biological processes in whole, living organisms. It can be used to observe anatomical structures, molecular/cellular activities, and metabolic functions as they occur more naturally within whole organisms. This is different from in vitro imaging, which refers to techniques used to examine processes in cultured cells.

Advantages of in vivo imaging:

  • Results taken from live animals are more biologically relevant
  • Real-time monitoring of animals can provide insights into dynamic events, such as tumor development

Challenges of in vivo imaging:

  • Higher cost of imaging equipment and animal care
  • Requires larger sample sizes and longer timelines

In Vivo Bioluminescence Imaging

In vivo bioluminescence imaging (BLI) is a non-invasive technique used for real-time monitoring of cellular and molecular processes within live organisms. Unlike other imaging modalities that may require the use of contrast agents or radiation, BLI relies solely on the light produced by bioluminescence reaction.

Advantages of In Vivo Bioluminescence Imaging

  • Non-toxic: Subjects can be repeatedly imaged over time without significant harm. This allows for longitudinal studies on disease progression and gene expression patterns. 
  • High sensitivity: The luciferase-luciferin reaction is highly efficient, producing a strong light signal with minimal background noise. This sensitivity enables the detection of very low levels of biological activity.

How Does In Vivo Bioluminescence Imaging Work?

In vivo BLI requires three main components:

  • Animal model expressing a luciferase reporter gene
  • Luciferase substrate
  • Imaging system 

The general process of in vivo BLI is as follows:

  1. Reporter animal model creation: An animal model expressing luciferase reporters, such as NanoLuc® or firefly luciferase, is created using genetic engineering techniques.
  2. Substrate administration: Luciferase substrate is administered into the animal, typically via injection. 
  3. Luminescence signal generation: When the substrate encounters luciferase in the presence of oxygen and ATP, it undergoes an enzymatic reaction that produces luminescence.
  4. Detection and imaging: Specialized imaging systems detect the luminescence signal and convert it into an image.
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Example in vivo bioluminescence imaging data. Mice were injected with increasing levels of AAV9-NanoLuc® and then 0.44μmoles FFz 7 and 13 days post transduction. Tissue tropism started to appear at 7 days, and a stronger signal and more extensive tissue tropism appeared after 13 days.

Reporters and Substrates for In Vivo Bioluminescence Imaging

The luminescence signal generated from luciferase reporters is dependent on the substrate, so selecting an appropriate substrate is crucial. We provide substrates optimized for the following reporters:

  • NanoLuc® Luciferase Detection: The Nano-Glo® Fluorofurimazine In Vivo Substrate (FFz) is designed specifically for in vivo detection of NanoLuc® Luciferase, NanoLuc® fusion proteins or reconstituted NanoBiT® Luciferase.
  • Firefly Luciferase Detection: VivoGlo™ Luciferin, In Vivo Grade is optimized for in vivo detection of firefly luciferase, firefly luciferase fusion proteins, or reconstituted firefly luciferase complexes.
  • NanoLuc® and Firefly Luciferase Dual Detection: Specificity of the above substrates allows NanoLuc® and firefly luciferases to be used together for dual-luciferase molecular imaging studies, providing even more options for creating whole animal reporter models.

Interested in our substrates designed for in vivo imaging?

Learn about Nano-Glo® FluorofurimazineLearn About VivoGlo™ Luciferin

In Vivo Bioluminescence Imaging Applications

Study Infectious Disease Dynamics

By using bioluminescent bacteria or viruses, researchers can non-invasively monitor the spread and localization of an infection in real-time within a living organism. This allows for the assessment of pathogen load, dissemination, and the host’s immune response over time, providing insights into disease mechanisms and the effectiveness of therapeutic interventions.

Cancer Progression

Tumor cells engineered to express luciferase can be tracked in vivo, allowing researchers to visualize and quantify tumor burden and metastatic spread longitudinally. This technique can be used to evaluate the efficacy of anti-cancer therapies, monitor tumor relapse, and study the biology of cancer cells in their native microenvironment.

Evaluate Gene Therapy Outcomes

By incorporating luciferase reporters into gene therapy vectors, researchers can assess the efficiency of gene delivery, expression levels, and the persistence of the therapeutic gene non-invasively over time. Real-time monitoring helps optimize gene therapy strategies, ensuring targeted and sustained gene expression.

Develop New Drugs and Therapies

In vivo BLI enables real-time evaluation of drug efficacy, pharmacokinetics, and biodistribution in live animals. This enables researchers to rapidly screen and identify promising therapeutic candidates, study drug mechanisms, and optimize dosing regimens.

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View these resources to learn more about in vivo BLI:

Article

Navigating In Vivo Bioluminescence Imaging

Starting with in vivo bioluminescent imaging can be challenging, especially when you're trying to get the most out your experiment. Read this technical article that covers everything you need to know about in vivo bioluminescence.

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Webinar

Advancing In Vivo Insights: Mastering Bioluminescent Imaging for Dynamic Biological Studies

Join this webinar to learn about the three basic elements of in vivo bioluminescent imaging: the bioluminescent reporter protein, reporter substrate, and detection instrument.

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Blog

Expert Insights: A Look Forward at Multiplexing for In Vivo Bioluminescence Imaging

Already using a luminescent reporter in vivo, and want to know the power of multiplexing? We asked some experts in the field about their opinion on the future of the technique. 

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In Vivo Fluorescence Imaging

In vivo fluorescence imaging (FLI) utilizes fluorescent probes or ligands, which emit light upon excitation by an external light source. 

Advantages of In Vivo Fluorescence Imaging

  • Multiplexing: Fluorescent probes are widely available for identification of protein and gene targets, enabling a wide variety of multiplexing possibilities.
  • Quick Analysis: Due to the high number of photons produced by fluorescent ligands, images can be captured with short exposure times, enabling quick analysis of fluorescent markers.

Disadvantages of In Vivo Fluorescence Imaging

  • Autofluorescence: Natural fluorescence from tissues can interfere with the signal from fluorescent probes, reducing contrast and accuracy.
  • Photobleaching: Prolonged exposure to light can cause fluorescent molecules to lose their ability to emit light, diminishing the quality of imaging over time. Thus, long-term kinetic studies may not be possible.
  • Toxicity: Some fluorescent dyes or probes can be toxic to living tissues, affecting the viability of the sample and the accuracy of the results.

Making BRET the Bright Choice for In Vivo Imaging: Use of NanoLuc® Luciferase with Fluorescent Protein Acceptors

Combining the strength of bioluminescence with fluorescence proteins has allowed researchers to make innovate tools that are not possible with other luciferases. This blog covers a publication that demonstrates the unique capabilities enabled through NanoBRET® Energy Transfer technology.

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