מחבר: Philip Ramirez

When you, scientists and researchers, approach the study of new drugs or to better understand existing ones, one of the central questions is how exactly this drug interacts with the cells in the human body. For many years, the tools available to you were often based on dead cells, or on components isolated from the cell that were tested in vitro. The main problem with these approaches is that a living cell is a world in itself – a dynamic, vibrant, and constantly changing system. Its behavior is much more complex than the sum of its individual parts. This is where live cell studies come into play, and they are a real revolution. They open up a unique window into this fascinating world, allowing you, the researchers, to observe closely how drugs work in their natural environment, the living cell. The great advantage is that they maintain the dynamic and multi-dimensional nature of cellular responses, thereby revealing complexities that static or simple biochemical tests simply cannot capture. Let's dive into the subject together and understand exactly how this happens, and what you can learn from it.

Real-Time Tracking of Dynamic Processes – Seeing the Drug in Action, Here and Now

One of the most significant and exciting advantages of working with live cells is the ability to track processes as they happen, in real time. Imagine sitting quietly and watching a fascinating documentary, where the cell is the main star responding to a drug that has just been introduced to it. This is completely different from looking at two separate still images, one of "before" and one of "after." Advanced imaging techniques and spectroscopic methods adapted to live cells, such as plasmonic-enhanced Raman spectroscopy – a particularly sensitive technique that allows the identification of specific molecules – or stimulated Raman scattering, allow you to do just that. Using these tools, you can monitor the effects of the drug kinetically, that is, see how things change and evolve from moment to moment, right before your eyes.

So what does it mean in practice when you apply these techniques in the lab?

• Drug uptake rate and distribution within the cell: You can measure and see exactly how quickly the drug manages to penetrate the cell membrane, which organelles or areas within the cell it reaches, and whether it tends to accumulate in certain places more than others. Such information is absolutely critical, as it helps you understand whether the drug even manages to reach its intended target within the cell, and how efficiently.
• Time-dependent biochemical changes: Drugs, by their very nature, cause biochemical changes in the cell, and this is often a chain of complex events. By continuously monitoring live cells, you can identify and document changes such as protein denaturation (i.e., a change in their spatial structure that impairs their proper function), the formation of damage to the cell's genetic material (DNA), or significant changes in the cell's metabolic pathways. The ability to see exactly when each change occurs, and in what order, is key to accurately deciphering the molecular mechanism of action of the drug.
• Cell adaptation mechanisms: Cells, as you know, are not passive creatures that accept their fate without reaction. They are intelligent systems that respond actively to their environment, and often develop sophisticated ways to deal with the challenges that drugs pose to them. In live cell studies, you can identify such adaptation mechanisms in real time, such as the development of resistance to a particular drug, or the activation of alternative biochemical pathways aimed at compensating for the original effect of the drug.

A classic and beautiful example of this comes from studies done on common chemotherapeutic drugs, such as fluorouracil, in cultured human breast cancer cells of the MCF-7 type. In these studies, where the researchers closely followed the cellular response over time, they were able to identify different delays in the response time and determine different rate constants for the changes caused to proteins and DNA in the cell. This detailed kinetic information made it possible to distinguish between the modes of action of the different drugs in a much sharper and more accurate way than was previously possible using static methods. It's like understanding not only what the drug does to the cell, but also when exactly it does it, at what rate, and how the different processes integrate with each other.

Multi-Target Effects and Off-Target Effects – The Big Picture of Drug Action

Many drugs, and perhaps most, are not "snipers" that act only on a single molecular target in the cell. In the complex reality of cell biology, drugs often have interactions with multiple targets. Some of these effects can be what are known as "off-target effects" – that is, effects on molecules or biochemical pathways that the drug was not designed to affect at all. Traditional biochemical tests, which usually focus on testing a specific interaction between a drug and an isolated target (for example, a purified enzyme in vitro), may completely miss this broad and complex picture.

This is exactly where live cell studies come into play and offer a significant advantage. Because you are examining the entire cell, with all its components and functioning systems, you can capture the entirety of the interactions that occur simultaneously. This holistic approach allows you to identify:

• Compounds with diverse and sometimes surprising pharmacological activities: There are compounds, such as brefeldin A or the flavonoid quercetin, that exhibit very different, and even seemingly contradictory, activities depending on the specific cellular context in which they are tested. For example, these compounds can in some situations inhibit the toxicity of a potent toxin such as ricin, and in other situations inhibit the growth of cancer cells that have become resistant to several drugs. These fascinating differences in activity are probably due to the interaction of the compounds with different targets or different biochemical pathways that are differentially activated in different cells or under different conditions.
• Identification of compounds that act against targets considered "undruggable targets": In the world of drug development, there are important biological targets for various diseases, against which it is very difficult to develop effective drugs using traditional discovery methods for structural or functional reasons. Phenotypic screens in whole cells – that is, screens in which you look for compounds that cause some observable change in the cell (phenotype), such as a change in shape, growth rate, or cell death – can lead to the identification of compounds that act against these "difficult" targets. An excellent example of this is the identification of new antibiotic molecules that act against the PanC enzyme, a vital target in certain bacteria that was previously considered difficult to attack.

The ability to see the multi-target effects and the off-target effects is of critical importance. It helps you better understand not only the full therapeutic potential of the drug, but also its possible side effects. If a drug hits unwanted targets in addition to its primary target, this can lead to toxicity, decreased treatment effectiveness, or other problems that are important to anticipate.

Mechanistic Insights in Physiologically Relevant Contexts – Understanding the How" and the "Why"

Beyond identifying the very existence of interactions between a drug and its targets, live cell studies provide you, the researchers, with deep and valuable insights into the molecular mechanisms by which drugs work. And all this, it is important to emphasize, takes place in the relevant and dynamic physiological context of the living and functioning cell. This is much richer and more informative information than just knowing that a certain drug binds to a specific target under controlled in vitro conditions.

• Activation of complex cellular pathways: By cleverly using genetically engineered fluorescent markers in live cells (for example, the BiFC technique – Bimolecular Fluorescence Complementation – which allows to visualize interactions between proteins in real time), you can track the complex dynamics of central signaling pathways within the cell. For example, you can see how a natural compound like apigenin, found in fruits and vegetables, affects important signaling pathways such as JAK/STAT or TGF-β1. You not only see that the pathway is activated or silenced as a result of drug treatment, but also how exactly this happens over time, what the intermediate stages are, and what the intensity of the response is.
• Functional implications at the whole cell level: While classic biochemical tests can clearly show you that a drug binds to a specific molecular target, live cell studies reveal the actual functional results of that binding at the whole cell level. Does this binding cause the cell to enter a pathway of apoptosis (programmed and controlled cell death)? Does it stop the cell's ability to divide and proliferate (proliferation arrest)? Does it affect the ability of cells to migrate, invade adjacent tissues, or heal wounds? These are critical questions whose answers lie in direct observation of the behavior of the living cell.
• Early stage toxicity and permeability testing: Another important advantage of working with live cells is the ability to immediately and directly identify compounds that do not manage to penetrate the cells at all, or those that cause general (cytotoxicity) and non-specific cellular toxicity. If a potential drug is unable to enter the cell, it will of course not be able to exert its desired effect. If it kills the cells indiscriminately and non-selectively, it is probably not a good candidate for clinical development. This information, obtained early in the drug discovery process, can save you valuable time and resources later on.

This deep mechanistic understanding, obtained from direct observation of the living and functioning cell in all its complexity, is a cornerstone in the development of more effective, more specific, and safer drugs for use. You get a much fuller and richer picture of what the drug does to the cell, and not just a small and specific part of the complex puzzle.

Advanced Imaging Techniques – Innovative Tools for Studying the Living Cell

The dizzying technological advances in the field of cellular imaging in recent years have opened up amazing and unprecedented possibilities for you, the research community, to study interactions between drugs and live cells. These techniques allow you not only to see the cell more clearly than ever before, but also to measure and quantify in real time dynamic processes that occur within it at high spatial and temporal resolution.

• Surface Plasmon Resonance (SPR) on live cells: This technique, which has been adapted in recent years to work with live cells, allows you to accurately quantify the binding between a drug and receptors or other molecules located on the surface of the live cell membrane. At the same time, you can use advanced fluorescent imaging techniques to track the intracellular effects that occur as a result of that binding on the cell surface. This powerful combination gives you a two-stage and complementary picture: what happens on the cell surface, and what happens inside it as a direct result.
• Stimulated Raman Scattering (SRS) microscopy: This is an advanced and particularly powerful optical technique that allows to demonstrate unlabeled drugs (i.e., drugs that have not been added with a fluorescent, radioactive or other tag) inside live cells and under physiological conditions as close as possible to their natural state in the body. For example, using SRS microscopy, researchers were able to demonstrate the experimental drug DDR1 inhibitor 7RH, an inhibitor of tyrosine kinase receptor, inside live cells, and track its distribution and movement. The ability to track drugs without the need for external labeling prevents the concern, which always exists, that the labeling itself will change the physicochemical properties of the drug, its interactions, or the behavior of the cell.

These techniques, and many others that are constantly being developed, are constantly expanding the sophisticated toolbox available to you in the fascinating study of drug-cell interactions. They allow you to ask more complex questions, examine bolder hypotheses, and get more accurate and detailed answers about how drugs work at the delicate cellular level. This is a research field that is developing at a dizzying pace, and promises more fascinating discoveries and breakthroughs in the near and distant future.

Limitations and Considerations – What is Important to Take into Account?

Despite the many and obvious advantages of live cell studies, it is important that you are also aware of the limitations and certain considerations involved in this approach. Understanding these points will help you plan experiments optimally, interpret the results obtained in a critical and correct way, and avoid erroneous conclusions.

click here for more info: databiotech.co.il