Soft Materials for Studying Hard Biological Problems

By Kristi S. Anseth

Chemical and Biological Engineering, University of Colorado at Boulder, Boulder, CO

Published on

Abstract

Our group focuses on the development of biomaterial matrices that can serve as advanced culture systems or in vivo delivery systems for primary cells. We exploit material chemistry as a tool to decipher how cells process signals from the extracellular matrix (ECM), and then use this information to design improved biomaterials that promote tissue regeneration. Specifically, we design synthetic ECM analogs that capture key features of the unique chemistry and physical properties of a cell’s niche—an environment that is not only tissue specific, but can be strikingly heterogeneous and dynamic. Unique to our approach is the ability to create cell-laden matrices in three-dimensional space in which the matrix properties can be changed on demand—so-called 4D biology. Here, our group has focused on the development of photochemical reactions to create tunable cell-laden matrices, for example, the thiol-ene photo-click reaction and complementary photo-clip reactions to introduce and remove biological signals from a complex milieu. These photochemical reactions not only proceed rapidly and with high specificity, but are bio-orthogonal, spatiotemporally controlled, and cytocompatible. This talk will illustrate how we leverage these and other reversible chemistries to create biologically responsive hydrogel matrices, and employ them to study the effects of matricellular signaling on diverse cellular functions and processes. For example, we exploit peptide-crosslinked PEG hydrogels to encapsulate stem cells and study how matrix density, degradability, elasticity, and adhesivity influence migration, proliferation, and differentiation. More recently, we have integrated photodegradable linkers into hydrogels and used these spatiotemporal controlled reactions to direct the growth and differentiation of stem cells into intestinal organoids.

Bio

Kristi S. Anseth Kristi S. Anseth is the Tisone Distinguished Professor of Chemical and Biological Engineering and Associate Faculty Director of the BioFrontiers Institute at the University of Colorado at Boulder. Her research interests lie at the interface between biology and engineering where she designs new biomaterials for applications in drug delivery and regenerative medicine. Dr. Anseth is an elected member of the National Academy of Engineering (2009), the National Academy of Medicine (2009), the National Academy of Sciences (2013), and the National Academy of Inventors (2016). She is also a Fellow of the American Association for the Advancement of Science, the American Institute for Medical and Biological Engineering, American Institute of Chemical Engineers, and the Materials Research Society. Dr. Anseth currently serves on the Board of Directors of the American Institute of Chemical Engineers, Board of Trustees for the Gordon Research Conferences, and is an editor for Biomacromolecules and Progress in Materials Science. She is a proud alumna of Purdue, receiving her BS in 1992 from the School of Chemical Engineering and an honorary doctorate in 2016.

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Cite this work

Researchers should cite this work as follows:

  • Kristi S. Anseth (2019), "Soft Materials for Studying Hard Biological Problems," https://nanohub.org/resources/31418.

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Location

Forney Hall, Room G140, Purdue University, West Lafayette, IN

Tags

Soft Materials for Studying Hard Biological Problems
  • Soft Materials for Studying Hard Biological Problems 1. Soft Materials for Studying Ha… 0
    00:00/00:00
  • Fundamental biological questions 2. Fundamental biological questio… 237.20387053720387
    00:00/00:00
  • Hydrogels 3. Hydrogels 376.71004337671008
    00:00/00:00
  • PEG-based hydrogels 4. PEG-based hydrogels 516.5165165165165
    00:00/00:00
  • PEG gels limit cell-matrix interactions 5. PEG gels limit cell-matrix int… 655.588922255589
    00:00/00:00
  • Dynamic niches for 4D cell culture 6. Dynamic niches for 4D cell cul… 791.89189189189187
    00:00/00:00
  • Orthogonal bio-click reactions 7. Orthogonal bio-click reactions 906.20620620620628
    00:00/00:00
  • Peptides as mimics of ECM Proteins 8. Peptides as mimics of ECM Prot… 1011.2445779112446
    00:00/00:00
  • Thiol-ene photo-click chemistry 9. Thiol-ene photo-click chemistr… 1114.2809476142809
    00:00/00:00
  • Thiol-ene chemistry 10. Thiol-ene chemistry 1181.6483149816484
    00:00/00:00
  • Mesenchymal stem cells 11. Mesenchymal stem cells 1233.1664998331667
    00:00/00:00
  • Thiol-ene reaction 12. Thiol-ene reaction 1321.9552886219553
    00:00/00:00
  • Mesenchymal stem cells 13. Mesenchymal stem cells 1367.6343009676343
    00:00/00:00
  • Healing critical sized bone defects 14. Healing critical sized bone de… 1389.7230563897231
    00:00/00:00
  • Dynamic niches for 4D cell culture 15. Dynamic niches for 4D cell cul… 1510.11011011011
    00:00/00:00
  • Stem cell-derived organoids 16. Stem cell-derived organoids 1568.0013346680014
    00:00/00:00
  • Intestinal organoids from single Lgr5+ crypt stem cells 17. Intestinal organoids from sing… 1686.986986986987
    00:00/00:00
  • Intestinal organoids in degradable PEG hydrogels 18. Intestinal organoids in degrad… 1887.8211544878213
    00:00/00:00
  • Dynamic hydrogel microenvironments 19. Dynamic hydrogel microenvironm… 2028.9622956289625
    00:00/00:00
  • Dynamic Matrices 20. Dynamic Matrices 2096.83016349683
    00:00/00:00
  • Photodegradable click hydrogels for culture of ISCs 21. Photodegradable click hydrogel… 2151.9519519519522
    00:00/00:00
  • Colony forming efficiency is dependent on gel modulus 22. Colony forming efficiency is d… 2215.5488822155489
    00:00/00:00
  • Photodegradation with focused 405 nm laser 23. Photodegradation with focused … 2261.9619619619621
    00:00/00:00
  • Crypt-like domains form in photodegraded regions 24. Crypt-like domains form in pho… 2355.1551551551552
    00:00/00:00
  • Lgr5+ and dividing cells localize to crypt structures 25. Lgr5+ and dividing cells local… 2401.8351685018351
    00:00/00:00
  • crypt morphology 26. crypt morphology 2441.5415415415418
    00:00/00:00
  • Crypt formation results in the differentiation of the absorptive and secretory cell types 27. Crypt formation results in the… 2456.122789456123
    00:00/00:00
  • Photodegradation leads to a localized change in shape of cells in the epithelium 28. Photodegradation leads to a lo… 2468.2682682682685
    00:00/00:00
  • How can you make systems? 29. How can you make systems? 2559.6262929596264
    00:00/00:00
  • Adaptable Networks 30. Adaptable Networks 2576.8768768768768
    00:00/00:00
  • Adaptable Materials 31. Adaptable Materials 2657.424090757424
    00:00/00:00
  • Adaptable hydrogels for regenerative biology 32. Adaptable hydrogels for regene… 2659.8264931598264
    00:00/00:00
  • Design of clickable allyl sulfide PEG crosslinkers 33. Design of clickable allyl sulf… 2723.3566900233568
    00:00/00:00
  • Amplified photodegradation with allyl sulfides 34. Amplified photodegradation wit… 2786.21955288622
    00:00/00:00
  • Thick gel degradation and capture and release of hMSCs 35. Thick gel degradation and capt… 2850.7507507507507
    00:00/00:00
  • Templated organoids 36. Templated organoids 2897.4307640974307
    00:00/00:00
  • Photoinduced network reorganization 37. Photoinduced network reorganiz… 2900.1001001001
    00:00/00:00
  • Photo-induced network reorganization 38. Photo-induced network reorgani… 2904.5378712045381
    00:00/00:00
  • Summary 39. Summary 2908.5085085085088
    00:00/00:00
  • Acknowledgments 40. Acknowledgments 3004.8048048048049
    00:00/00:00
  • Thank you! 41. Thank you! 3043.9773106439775
    00:00/00:00