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Characterizing the dynamic rheology in the pericellular region by human mesenchymal stem cell re-engineering in PEG-peptide hydrogel scaffolds

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Abstract

During wound healing, human mesenchymal stem cells (hMSCs) migrate to injuries to regulate inflammation and coordinate tissue regeneration. To enable migration, hMSCs re-engineer the extracellular matrix rheology. Our work determines the correlation between cell-engineered rheology and motility. We encapsulate hMSCs in a cell-degradable peptide-polymeric hydrogel and characterize the change in rheological properties in the pericellular region using multiple particle tracking microrheology. Previous studies determined that pericellular rheology is correlated with motility. Additionally, hMSCs re-engineer their microenvironment by regulating cell-secreted enzyme, matrix metalloproteinases (MMPs), activity by also secreting their inhibitors, tissue inhibitors of metalloproteinases (TIMPs). We independently inhibit TIMPs and measure two different degradation profiles, reaction-diffusion and reverse reaction-diffusion. These profiles are correlated with cell spreading, speed and motility type. We model scaffold degradation using Michaelis-Menten kinetics, finding a decrease in kinetics between joint and independent TIMP inhibition. hMSCs ability to regulate microenvironmental remodeling and motility could be exploited in design of new materials that deliver hMSCs to wounds to enhance healing.

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References

  • abcam (2018) buffer and stock solutions for western blot. https://www.abcamcom/protocols/buffer-and-stock-solutions-for-western-blot

  • Adolf D, Martin JE (1990) Time-cure superposition during crosslinking. Macromolecules 23:3700–3704

    Article  Google Scholar 

  • Aimetti AA, Machen AJ, Anseth KS (2009) Poly(ethylene glycol) hydrogels formed by thiol-ene photopolymerization for enzyme-responsive protein delivery. Biomaterials 30:6048–6054

    Article  Google Scholar 

  • Anderson SB, Lin CC, Kuntzler DV, Anseth KS (2011) The performance of human mesenchymal stem cells encapsulated in cell-degradable polymer-peptide hydrogels. Biomaterials 32:3564–3574

    Article  Google Scholar 

  • Bassi EJ, Candido de ALmeida D, Moraes-Vieira PMM, Camara NOS (2012) Exploring the role of soluble factors associated with immune regulatory properties of mesenchymal stem cells. Stem Cell Rev and Rep 8:329–342

    Article  Google Scholar 

  • Bear JE, Haugh JM (2014) Directed migration of mesenchymal cells: where signaling and the cytoskeleton meet. Curr Opin in Cell Biology 30:78–82

    Article  Google Scholar 

  • Benton JA, Fairbanks BD, Anseth KS (2009) Characterization of valvular interstitial cell function in three dimensional matrix metalloproteinase degradable PEG hydrogels. Biomaterials 30: 6593–6603

    Article  Google Scholar 

  • Bloom RJ, George JP, Celedon A, Sun SX, Wirtz D (2008) Mapping local matrix remodeling induced by a migrating tumor cell using three-dimensional multiple-particle tracking. Biophys J 95:4077–4088

    Article  Google Scholar 

  • Brew K, Nagase H (2010) The tissue inhibitors of metalloproteinases (TIMPs): an ancient family with structural and functional diversity. Biochim Biophys Acta 1(1803):55–71

    Article  Google Scholar 

  • Brew K, Dinakarpandian D, Nagase H (2000) Tissue inhibitors of metalloproteinases: evolution, structure and function. Biochemica et Biophysica Acta 1477:267–283

    Article  Google Scholar 

  • Bryant SJ, Anseth KS (2003) Controlling the spatial distribution of ECM components in degradable PEG hydrogels for tissue engineering cartilage. Biomed Mater Res 64A:70–79

    Article  Google Scholar 

  • Buxboim A, Ivanovska IL, Discher DE (2010) Matrix elasticity, cytoskeletal forces and physics of the nucleus: how deeply do cells ‘feel’ outside and in? Cell Science 123:297–308

    Article  Google Scholar 

  • Caplan AI (2009) Why are MSCs therapeutic? New data: new insight. J Pathol 217:318–324

    Article  Google Scholar 

  • Chambon F, Winter HH (1987) Linear viscoelasticity at the gel point of a crosslinking PDMS with imbalanced stoichiometry. J Rheol 31:683–697

    Article  Google Scholar 

  • Cheng Y, Prudhomme RK (2000) Enzymatic degradation of guar and substituted guar galactomannans. Biomacromolecules 1:782–788

    Article  Google Scholar 

  • Corrigan AM, Donald AM (2009) Passive microrheology of solvent-induced fibrillar protein networks. Langmuir 25:8599–8605

    Article  Google Scholar 

  • Cox TR, Erler JT (2009) Remodeling and homeostasis of the extracellular matrix: implications for fibrotic diseases and cancer. Disease Models and Mechanisms 4:165–178

    Article  Google Scholar 

  • Crocker JC, Grier DG (1996) Methods of digital video microscopy for colloidal studies. J Colloid Interface Sci 179:298–310

    Article  Google Scholar 

  • Crocker JC, Weeks ER (2011) Particle tracking using idl. http://www.physicsemoryedu/faculty/weeks//idl/

  • Daviran M, Caram HS, Schultz KM (2018a) Role of cell-mediated enzymatic degradation and cytoskeletal tension on dynamic changes in the rheology of the pericellular region prior to human mesenchymal stem cell motility. ACS Biomater Sci Eng 4:468–472

    Article  Google Scholar 

  • Daviran M, Longwill SM, Casella JF, Schultz KM (2018b) Rheological characterization of dynamic remodeling of the pericellular region by human mesenchymal stem cell-secreted enzymes in well-defined synthetic hydrogel scaffolds. Soft Matter 14:3078–3089

    Article  Google Scholar 

  • Eggenhofer E, Luk F, Dahlke MH, Hoogduijn MJ (2014) The life and fate of mesenchymal stem cells. Front Immunol 5:148–1–148-6

    Article  Google Scholar 

  • Engler AJ, Sen S, Lee Sweeney H, Discher DE (2006) Matrix elasticity directs stem cell lineage specification. Cell 126:677–689

    Article  Google Scholar 

  • Escobar F, Anseth KS, Schultz KM (2017) Dynamic changes in material properties and degradation of poly(ethylene glycol)hydrazone gels as a function of pH. Macromolecules 50:7351–7360

    Article  Google Scholar 

  • Fairbanks BD, Schwartz MP, Bowman CN, Anseth KS (2009) Photoinitiated polymerization of PEG-diacrylate with lithium phenyl-2,4,6-trimethylbenzoylphosphinate: polymerization rate and cytocompatibility. Biomaterials 30:6702–6707

    Article  Google Scholar 

  • Ferreira LS, Gerecht S, Fuller J, Shieh HF, Vunjak-Novakovic G, Langer R (2007) Bioactive hydrogel scaffolds for controllable vascular differentiation of human embryonic stem cells bioactive hydrogel scaffolds for controllable vascular differentiation of human embryonic stem cells. Biomaterials 28:2706–2717

    Article  Google Scholar 

  • Ferry JD (1980) Viscoelastic properties of polymers. Wiley, New York

    Google Scholar 

  • Friedl P (2004) Prespecification and plasticity: shifting mechanisms of cell migration. Curr Opin Cell Biol 16:14–23

    Article  Google Scholar 

  • Furst EM, Squires TM (2017) Microrheology, 1st edn. Oxford University Press, Oxford

    Google Scholar 

  • Grim JC, Marozas IA, Anseth KS (2015) Thiol-ene and photo-cleavage chemistry for controlled presentation of biomolecules in hydrogels. J Controlled Release 219:95–106

    Article  Google Scholar 

  • Guvendiren M, Burdick JA (2013) Engineering synthetic hydrogel microenvironments to instruct stem cells. Curr Opin in Biotech 24:841–846

    Article  Google Scholar 

  • Jackson WM, Nesti LJ, Tuan RS (2012) Concise review: Clinical translation of wound healing therapies based on mesenchymal stem cells. Stem Cells Transl Med 1:44–50

    Article  Google Scholar 

  • Kawada H, Fujita J, Kinjo K, Matsuzaki Y, Tsuma M, Miyatake H, Muguruma Y, Tsuboi K, Itabashi Y, Ikeda Y, Ogawa S, Okano H, Hotta T, Ando K, Fukuda K (2004) Nonhematopoietic mesenchymal stem cells can be mobilized and differentiate into cardiomyocytes after myocardial infarction. Blood 104:3581–3587

    Article  Google Scholar 

  • Kloxin AM, Kloxin CJ, Bowman CN, Anseth KS (2010) Mechanical properties of cellularly responsive hydrogels and their experimental determination. Biomaterials 22:3484–3494

    Google Scholar 

  • Kyburz KA, Anseth KS (2013) Three-dimensional hMSC motility within peptide-functionalized PEG-based hydrogels of varying adhesivity and crosslinking density. Acta Biomater 9:6381–6392

    Article  Google Scholar 

  • Larsen T, Schultz K, Furst EM (2008) Hydrogel microrheology near the liquid-solid transition. Korea-Australia Rheology Journal 20:165–173

    Google Scholar 

  • Larsen TH, Furst EM (2008) Microrheology of the liquid-solid transition during gelation. Phys Rev Lett 100:146001–4

    Article  Google Scholar 

  • Latifi-Pupovci H, Kuçi Z, Wehner S, Bönig H, Lieberz R, Klingebiel T, Bader P, Kuçi S (2015) In vitro migration and proliferation (“wound healing”) potential of mesenchymal open access stromal cells generated from human cd271 bone marrow mononuclear cells. J Transl Med 13:315–323

    Article  Google Scholar 

  • Lauffenburger DA, Horwitz AF (1996) Cell migration: a physically integrated molecular process. Cell 84:359–369

    Article  Google Scholar 

  • Legant WR, Miller JS, Blakely BL, Cohen DM, Genin GM, Chen CS (2010) Measurement of mechanical tractions exerted by cells in three-dimensional matrices. Nat Methods 7:969–973

    Article  Google Scholar 

  • Longhurst CM, Jennings LK (1998) Integrin-mediated signal transduction. Cell Mol Life Sci 54:514–526

    Article  Google Scholar 

  • Lozito TP, Tuan RS (2011) Endothelial cell microparticles act as centers of matrix metalloproteinsase-2 (MMP-2) activation and vascular matrix remodeling. Cell Physiology 227:534–549

    Article  Google Scholar 

  • Lozito TP, Jackson WM, Nesti LJ, Tuan RS (2014) Human mesenchymal stem cells generate a distinct pericellular zone of MMP activities via binding of MMPs and secretion of high levels of TIMPs. Matrix Biol 34:132–143

    Article  Google Scholar 

  • Lutolf MP, Lauer-Fields JL, Schoekel HG, Metters AT, Weber FE, Fields GB, Hubbell JA (2003) Synthetic matrix metalloproteinase-sensitive hydrogels for the conduction of tissue regeneration: engineering cell-invasion characteristics. PNAS 100:5413–5418

    Article  Google Scholar 

  • Mackenzie TC, Flake AW (2001) Human mesenchymal stem cells persist, demonstrate site-specific multipotential differentiation, and are present in sites of wound healing and tissue regeneration after transplantation into fetal sheep. Blood Cell Mol Dis 27:601–604

    Article  Google Scholar 

  • Maskarine SA, Franck C, Tirrell DA, Ravichandran G (2009) Quantifying cellular traction forces in three dimensions. PNAS 106:22108–22113

    Article  Google Scholar 

  • Mason TG, Weitz DA (1995) Optical measurements of frequency-dependent linear viscoelastic moduli of complex fluids. Phys Rev Lett 74(7):1250–1253

    Article  Google Scholar 

  • Mason TG, Ganesan K, van Zanten JH, Wirtz D, Kuo SC (1997) Particle tracking microrheology of complex fluids. Phys Rev Lett 79:3282–3285

    Article  Google Scholar 

  • Mazzeo MS, Chai T, Daviran M, Schultz KM (2019) Characterization of the kinetics and mechanism of degradation of human mesenchymal stem cell-laden poly(ethylene glycol) hydrogels. ACS Appl Bio Mater 2:81–92

    Article  Google Scholar 

  • Metzger S, Blache U, Lienemann PS, Karlsson M, Weber FE, Weber W, Ehrbar M (2016) Cell-mediated proteolytic release of growth factors from poly(ethylene glycol) matrices. Macromol Biosci 16:1703–1713

    Article  Google Scholar 

  • Miller JS, Shen CJ, Legant WR, Baranski JD, Blakely BL, Chen CS (2010) Bioactive hydrogels made from step-growth derived PEG-peptide macromers. Biomaterials 31:3736–3743

    Article  Google Scholar 

  • Munevar S, Wang Y, Dembo M (2001) Traction force microscopy of migrating normal and h-ras transformed 3t3 fibroblasts. Biophys J 80:1744–1757

    Article  Google Scholar 

  • Muthukumar M, Winter HH (1986) Fractal dimension of a crosslinking polymer at the gel point. Macromolecules 19:1284–1285

    Article  Google Scholar 

  • Nagase H, Visse R, Murphy G (2006) Structure and function of matrix metalloproteinases and timps. Cardiovasc Res 69:562–573

    Article  Google Scholar 

  • Olson MW, Gervasi DC, Mobashery S, Fridman R (1997) Kinetic analysis of the binding of human matrix metalloproteinase-2 and -9 to tissue inhibitor of metalloproteinase TIMP-1 and TIMP-2. Biol Chem 272 (47):29975–29983

    Article  Google Scholar 

  • Palmer A, Xu J, Wirtz D (1998) High-frequency viscoelasticity of crosslinked actin filament networks measured by diffusing wave spectroscopy. Rheol Acta 33:97–106

    Article  Google Scholar 

  • Patterson J, Hubbell JA (2010) Enhanced proteolytic degradation of molecularly engineered PEG hydrogels in response to MMP-1 and MMP-2. Biomaterials 31:7836–7845

    Article  Google Scholar 

  • Peppas NA, Hilt JZ, Khademhosseini A, Langer R (2006) Hydrogels in biology and medicine: From molecular principles to bionanotechnology. Adv Mater 18:1345–1360

    Article  Google Scholar 

  • Peyton SR, Raub CB, Keschrumrus VP, Putnam AJ (2006) The use of poly(ethylene glycol) hydrogels to investigate the impact of ECM chemistry and mechanics on smooth muscle cells. Biomaterials 27:4881–4893

    Article  Google Scholar 

  • Piperigkou Z, Götte M, Theocharis AD, Karamanos NK (2017) Insights into the key roles of epigenetics in matrix macromolecules-associated wound healing. Adv Drug Deliv Rev 129:16–36

    Article  Google Scholar 

  • Ponte AL, Marais E, Gallay N, Langonne A, Delorme B, Herault O, Charbord P, Domenech J (2007) The in vitro migration capacity of human bone marrow mesenchymal stem cells: comparison of chemokine and growth factor chemotactic activities. Stem Cells 25:1737–1745

    Article  Google Scholar 

  • Raeber GP, Lutolf MP, Hubbell JA (2007) Mechanisms of 3-d migration and matrix remodeling of fibroblasts within artificial ECMs. Acta Biomater 3:615–629

    Article  Google Scholar 

  • Rice MA, Sanchez-Adams J, Anseth KS (2006) Exogenously triggered, enzymatic degradation of photopolymerized hydrogels with polycaprolactone subunits: experimental observation and modeling of mass loss behavior. Biomacromolecules 7:1968–1975

    Article  Google Scholar 

  • Ries C, Egea V, Karow M, Kolb H, Jochum M, Neth P (2007) MMP-2, MT1-MMP, and TIMP-2 are essential for the invasive capacity of human mesenchymal stem cells: differential regulation by inflammatory cytokines. Blood 109(9):4055–4063

    Article  Google Scholar 

  • RnDsystem (2018a) Antibodies. https://www.rndsystems.com/products/human-mouse-timp-2-antibody_af971

  • RnDsystem (2018b) Antibodies. https://www.rndsystems.com/products/human-timp-1-antibody_af970

  • Savin T, Doyle PS (2005) Static and dynamic errors in particle tracking microrheology. Biophys J 88:623–638

    Article  Google Scholar 

  • Schultz KM, Anseth KS (2013) Monitoring degradation of matrix metalloproteinases cleavable PEG hydrogels via multiple particle tracking microrheology. Soft Matter 9:1570–1579

    Article  Google Scholar 

  • Schultz KM, Furst EM (2012) Microrheology of biomaterial hydrogelators. Soft Matter 8:6198–6205

    Article  Google Scholar 

  • Schultz KM, Bayles AV, Baldwin AD, Kiick KL, Furst EM (2011) Rapid, high resolution screening of biomaterial hydrogelators by μ 2rheology. Biomacromolecules 12:4178–4182

    Article  Google Scholar 

  • Schultz KM, Baldwin AD, Kiick KL, Furst EM (2012) Measuring the modulus and reverse percolation transition of a degrading hydrogel. ACS Macro Lett 1:706–708

    Article  Google Scholar 

  • Schultz KM, Kyburz KA, Anseth KS (2015) Measuring dynamic cell-material interactions and remodeling during 3d human mesenchymal stem cell migration in hydrogels. PNAS 112(29):E3757–E3764

    Article  Google Scholar 

  • Schwartz MP, Fairbanks BD, Rogers RE, Rangarajan R, Zaman MH, Anseth KS (2010) A synthetic strategy for mimicking the extracellular matrix provides insight about tumor cell migration. Integr Biol 2:32–40

    Article  Google Scholar 

  • Singer AJ, Clark RA (1999) Cutaneous wound healing. N Engl J Med 341:738–746

    Article  Google Scholar 

  • Soiné JRD, Brand CA, Stricker J, Oakes PW, Gardel ML, Schwarz US (2015) Model-based traction force microscopy reveals differential tension in cellular actin bundles. PLOS Comput Biol 11:e1004076

    Article  Google Scholar 

  • Squires TM, Mason TG (2010) Fluid mechanics of microrheology. Annu Rev Fluid Mech 42:413–438

    Article  Google Scholar 

  • Stauffer D, Coniglio A, Adam M (1982) Gelation and critical phenomena. Adv Polym Sci 44:103–158

    Article  Google Scholar 

  • Suga K, Dedem GV, Moo-Young M (1975) Enzymatic breakdown of water insoluble substrates. Biotechnol Bioeng 17:185–201

    Article  Google Scholar 

  • Tse JR, Engler AJ (2011) Stiffness gradients mimicking in vivo tissue variation regulate mesenchymal stem cell fate. PLoS one 6:e15978

    Article  Google Scholar 

  • Vincent LG, Choi YS, Alonso-Latorre B, del Álamo JC, Engler AJ (2013) Mesenchymal stem cell durotaxis depends on substrate stiffness gradient strength. Biotechnol J 8:472–484

    Article  Google Scholar 

  • Vu TH, Werb Z (2000) Matrix metalloproteinases: effectors of development and normal physiology. Genes Dev 14:2123–2133

    Article  Google Scholar 

  • Waigh TA (2005) Microrheology of complex fluids. Rep Prog Phys 68:685–742

    Article  Google Scholar 

  • Wehrman MD, Lindberg S, Schultz KM (2016) Quantifying the dynamic transition of hydrogenated castor oil gels measured via multiple particle tracking microrheology. Soft Matter 12:6463–6472

    Article  Google Scholar 

  • Wehrman MD, Lindberg S, Schultz KM (2018) Impact of shear on the structure and rheological properties of a hydrogenated castor oil colloidal gel during dynamic phase transitions. J Rheol 62:437–446

    Article  Google Scholar 

  • West JL, Hubbell JA (1999) Polymeric biomaterials with degradation sites for proteases involved in cell migration. Macromolecules 32:241–244

    Article  Google Scholar 

  • Winter HH (1987) Can the gel point of a cross-linking polymer be detected by the G’-G” crossover? Polym Eng Sci 27:1698–1702

    Article  Google Scholar 

  • Wolf K, Te Lindert M, Krause M, Alexander S, Te Riet J, Willis AL, Hoffman RM, Figdor CG, Weiss SJ, Friedl P (2013) Physical limits of cell migration: control by ECM space and nuclear deformation and tuning by proteolysis and traction force. Cell Biol 7(201):1069–1084

    Article  Google Scholar 

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Acknowledgements

We thank Dr. Susan Perry from the Department of Bioengineering at Lehigh University for her useful discussion on Western blot experiments. Research reported in this publication was supported by the National Institute of General Medical Sciences of the National Institutes of Health under award number R15GM119065. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

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Correspondence to Kelly M. Schultz.

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Daviran, M., Schultz, K.M. Characterizing the dynamic rheology in the pericellular region by human mesenchymal stem cell re-engineering in PEG-peptide hydrogel scaffolds. Rheol Acta 58, 421–437 (2019). https://doi.org/10.1007/s00397-019-01142-2

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