things to a lot of different people. The original versions of
biomaterials were thought to be inert materials you could implant in the body to help in the healing response. And so these were typically static implants, we think about artificial knees, artificial hips, the metal fixation devices they use in craniofacial surgery where you have to support the mandible if you're taking out a big bit of the bone after a tumor, for example. Instead of having the bone grow back, there are these strips of metal you can implant to hold everything in place. And so the original idea of a biomaterials is there is something inert, they could sit in a tissue or be affixed to a tissue and wouldn't drive any sort of long term chronic inflammatory response or infection response and that's changed over the years. It's become more active materials. So now we have, instead of a piece of metal being used as an artificial heart valve, you have decellularized heart valves that are used that have actual tissue properties to them that cells can grow back into and produce a native tissue again. We have biomaterials that my lab works in. The idea being some sort of porous structure that you could use to support cells. So we're interested in creating a kitchen sponge like materials or Jell-O like materials that are three-dimensional, that can hold cells in defined architectures will provide signals to them. They can be implanted in the body to help heal. But also recently, the idea of biometriotics extended outside of the body. One of the largest and fastest growing areas of research these days is this idea of tissue on a chip and this idea where you could take the complexity of a tissue, and take out of that a defined sequence of keys that you can produce in the laboratory. So you could grow tissues in the lab and this has a lot of advantages in terms of using them to test new drugs to measure cytotoxicity, something that is really difficult to do unless you have some sort of tissue like structure you work with. And so, biomaterials can mean a lot of things to a lot of different people. But from the basis, it's this idea of some sort of material structure whether it is a piece of metal, whether it's a sponge type material, whether it's a dense gel or whether it's a flat substrate. It is some sort of material property that has some sort of biological feature to it whether it's implanted in the body or used in the laboratory, there's a wide range of what biomaterials might be and a wide range of what research has done with them. And what that means is there's also a lot of really exciting advances that will be happening in the next few years as we continue to push the definition of what a biomaterial actually is. My lab focuses on the idea of developing instructive biomaterials. And so what that means is that you have a cell that could be sitting in a vacuum and is going to be doing something, and the cells are the building block of all the tissues, and organs in our body. And for a long time, the idea of materials that were used in medicine, they were meant to be inert or passive, so that it allowed the cells to do whatever the cell was going to do and the material was there to support the cells in some manner. So, one example might be an artificial hip implant. The goal is not to instruct the cells in the femur to do anything new, it's simply to replace the femur with a lump of titanium and that makes the joint functional, but it's not providing any instructive signal to the surrounding tissues. And so the sort of paradigm shift that we're working on is how do you design materials that are in cells instructive, that could take the cells from the surrounding wound site and instruct them to do different types of processes to aid the healing process. So that in the end, you're left with the native tissue again and it´s a subtle paradigm shift, but what it gets us thinking about is how would you want to instruct cells, what type of signals would you want to provide to them. Would it be in the form of mechanical ques, structural ques, chemical ques and how do you layer them together in order to obtain some sort of desired biological output? So fortunately or unfortunately, the biology of a cell is extraordinarily complex. And so what you see is a cell that will have the same genome can turn into many different cell types, if you're talking about stem cells differentiating into mature cells. What that also means is that these transcription factors can be used for many different things. So transcription factors that could be upregulated in development can also be used when they're upregulated to prevent cancers from that are responsible for some cancers being harder to treat and it's all about the context in which these transcription factors are presented, what sequence they are presented in. What other features are being activated in the cell at the same time and that's why a lot of these studies are so complex and time-consuming, but have such a big payoff. because if you could imagine unlocking the code of how you would sequentially express a series of transcription factors or a series of signals to drive particular patterns of transcription factor activation, you could unlock the ability to get cells to do what you want. And that would give us the master code to cure cancer, to regenerate whole limbs, to really address these things that we have no ability to deal with today, but that you would hope a decade from now or a generation from now or a century from now, we absolutely will be doing on a regular basis. And it's the hard work right now understanding how all these different pathways are interrelated, how some things are up regulated and down regulated in disease and development and normal life that'll give us the cues to understand how do we do that in an engineering context where you want to show up, provide the right signals. Drive the particular response. Measure that response and then move from there. [MUSIC]