headshot of George Hussey

George Hussey

Assistant Professor
Bioengineering Department

overview

The primary focus of my research program is the discovery, development, and clinical translation of extracellular matrix (ECM)-based and other natural biopolymer materials for functional tissue reconstruction. These interests also extend into an in-depth understanding of the molecular mechanisms of constructive tissue remodeling, specifically in examining the host remodeling response and the effect of biomaterials on immunomodulation, with the broad goal of identifying molecular targets to regulate these effects. Bio-interface interactions, including the role of biopolymers, constitutive phospholipids and incorporated (extracellular) RNA on matrix biology and the host tissue response, are prime targets of my investigations. My research program utilizes the full spectrum of investigative platforms including biochemical and molecular approaches, cell signal transduction, bioengineering and biomaterial science, computational modeling, and preclinical animal studies. The overall objective is to understand the mechanisms of host-biomaterial interactions, and to utilize those interactions for improved clinical outcomes to repair tissue damaged by trauma, disease or ageing. A second arm of my research is focused on the development of methods and processes that can advance production of ECM-based therapies from laboratory protocols to large-scale, cGMP-compatible manufacturing processes, and enable the rapid clinical translation of the next generation of regenerative medicine-based therapies. Over the past decade, these research pursuits have culminated in over 33 peer reviewed scientific publications and 11 patent applications that focus on development of new technologies to repair tissue after traumatic injury or disease. I currently serve as Co-PI or Co-Investigator on numerous DARPA, Medical Technology Enterprise Consortium (MTEC), NIH and Industry funded research; and I am a co-leader of a laboratory that consists of 4 staff scientists, 3 postdoctoral fellows, 3 predoctoral students, 8 undergraduate students, a technical support staff, and an administrative support staff. The laboratory is an active training environment for scientists in various career stages. In addition to my academic duties, I am a scientific co-founder and Vice President of Research and Development at ECM Therapeutics, Inc., a clinical stage regenerative medicine startup company that aims to develop and commercialize regenerative medicine-based products for clinical use. I am fortunate from these experiences to have participated in the full range of translational science, from initial observations in the laboratory to the development of clinical interventions

about

PhD, Cleveland State University

Crum, R.J., Capella-Monsonis, H., Chang, J., Dewey, M.J., Kolich, B.D., Hall, K.T., El-Mossier, S.O., Nascari, D.G., Hussey, G.S., & Badylak, S.F. (2023). Biocompatibility and biodistribution of matrix-bound nanovesicles in vitro and in vivo. ACTA BIOMATERIALIA, 155, 113-122.Elsevier BV. doi: 10.1016/j.actbio.2022.11.026.

Crum, R.J., Huckestien, B.R., Dwyer, G., Mathews, L., Nascari, D.G., Hussey, G.S., Turnquist, H.R., Alcorn, J.F., & Badylak, S.F. (2023). Mitigation of influenza-mediated inflammation by immunomodulatory matrix-bound nanovesicles. SCIENCE ADVANCES, 9(20), eadf9016.American Association for the Advancement of Science (AAAS). doi: 10.1126/sciadv.adf9016.

Behre, A., Tashman, J.W., Dikyol, C., Shiwarski, D.J., Crum, R.J., Johnson, S.A., Kommeri, R., Hussey, G.S., Badylak, S.F., & Feinberg, A.W. (2022). 3D Bioprinted Patient-Specific Extracellular Matrix Scaffolds for Soft Tissue Defects. ADVANCED HEALTHCARE MATERIALS, 11(24), e2200866.Wiley. doi: 10.1002/adhm.202200866.

Cramer, M., Molina, C.P., Hussey, G., Turnquist, H.R., & Badylak, S.F. (2022). Transcriptomic Regulation of Macrophages by Matrix-Bound Nanovesicle-Associated Interleukin-33. TISSUE ENGINEERING PART A, 28(19-20), 867-878.Mary Ann Liebert Inc. doi: 10.1089/ten.tea.2022.0006.

Crum, R.J., Capella-Monsonis, H., Badylak, S.F., & Hussey, G.S. (2022). Extracellular Vesicles for Regenerative Medicine Applications. APPLIED SCIENCES-BASEL, 12(15), 7472.MDPI AG. doi: 10.3390/app12157472.

Crum, R.J., Hall, K., Molina, C.P., Hussey, G.S., Graham, E., Li, H., & Badylak, S.F. (2022). Immunomodulatory matrix-bound nanovesicles mitigate acute and chronic pristane-induced rheumatoid arthritis. NPJ REGENERATIVE MEDICINE, 7(1), 13.Springer Science and Business Media LLC. doi: 10.1038/s41536-022-00208-9.

Murdock, M.H., Hussey, G.S., Chang, J.T., Hill, R.C., Nascari, D.G., Rao, A.V., Hansen, K.C., Foley, L.M., Hitchens, T.K., Amankulor, N.M., & Badylak, S.F. (2022). A liquid fraction of extracellular matrix inhibits glioma cell viability in vitro and in vivo. Oncotarget, 13(1), 426-438.Impact Journals, LLC. doi: 10.18632/oncotarget.28203.

Turner, N.J.J., Quijano, L.M.M., Hussey, G.S.S., Jiang, P., & Badylak, S.F.F. (2022). Matrix Bound Nanovesicles Have Tissue-Specific Characteristics That Suggest a Regulatory Role. TISSUE ENGINEERING PART A, 28(21-22), 879-892.Mary Ann Liebert Inc. doi: 10.1089/ten.tea.2022.0091.

Molina, C.P., Hussey, G.S., Liu, A., Eriksson, J., D'Angelo, W.A., & Badylak, S.F. (2021). Role of 4-hydroxybutyrate in increased resistance to surgical site infections associated with surgical meshes. BIOMATERIALS, 267, 120493.Elsevier BV. doi: 10.1016/j.biomaterials.2020.120493.

Hussey, G.S., Molina, C.P., Cramer, M.C., Tyurina, Y.Y., Tyurin, V.A., Lee, Y.C., El-Mossier, S.O., Murdock, M.H., Timashev, P.S., Kagan, V.E., & Badylak, S.F. (2020). Lipidomics and RNA sequencing reveal a novel subpopulation of nanovesicle within extracellular matrix biomaterials. SCIENCE ADVANCES, 6(12), eaay4361.American Association for the Advancement of Science (AAAS). doi: 10.1126/sciadv.aay4361.

Hussey, G.S., Nascari, D.G., Saldin, L.T., Kolich, B., Lee, Y.C., Crum, R.J., El-Mossier, S.O., D'Angelo, W., Dziki, J.L., & Badylak, S.F. (2020). Ultrasonic cavitation to prepare ECM hydrogels. ACTA BIOMATERIALIA, 108, 77-86.Elsevier BV. doi: 10.1016/j.actbio.2020.03.036.

Li, T., Zhang, Z., Bartolacci, J.G., Dwyer, G.K., Liu, Q., Mathews, L.R., Velayutham, M., Roessing, A.S., Lee, Y.C., Dai, H., Shiva, S., Oberbarnscheidt, M.H., Dziki, J.L., Mullet, S.J., Wendell, S.G., Wilkinson, J.D., Webber, S.A., Wood-Trageser, M., Watkins, S.C., Demetris, A.J., Hussey, G.S., Badylak, S.F., & Turnquist, H.R. (2020). Graft IL-33 regulates infiltrating macrophages to protect against chronic rejection. JOURNAL OF CLINICAL INVESTIGATION, 130(10), 5397-5412.American Society for Clinical Investigation. doi: 10.1172/JCI133008.

Hussey, G.S., Dziki, J.L., Lee, Y.C., Bartolacci, J.G., Behun, M., Turnquist, H.R., & Badylak, S.F. (2019). Matrix bound nanovesicle-associated IL-33 activates a pro-remodeling macrophage phenotype via a non-canonical, ST2-independent pathway. J Immunol Regen Med, 3, 26-35.Elsevier BV. doi: 10.1016/j.regen.2019.01.001.

Molina, C.P., Hussey, G.S., Eriksson, J., Shulock, M.A., Bonilla, L.L.C., Giglio, R.M., Gandhi, R.M., Sicari, B.M., Wang, D., Londono, R., Faulk, D.M., Turner, N.J., & Badylak, S.F. (2019). 4-Hydroxybutyrate Promotes Endogenous Antimicrobial Peptide Expression in Macrophages. TISSUE ENGINEERING PART A, 25(9-10), 693-706.Mary Ann Liebert Inc. doi: 10.1089/ten.tea.2018.0377.

Murdock, M.H., Chang, J.T., Luketich, S.K., Pedersen, D., Hussey, G.S., D'Amore, A., & Badylak, S.F. (2019). Cytocompatibility and mechanical properties of surgical sealants for cardiovascular applications. JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 157(1), 176-183.Elsevier BV. doi: 10.1016/j.jtcvs.2018.08.043.

Saldin, L.T., Patel, S., Zhang, L., Huleihel, L., Hussey, G.S., Nascari, D.G., Quijano, L.M., Li, X., Raghu, D., Bajwa, A.K., Smith, N.G., Chung, C.C., Omstead, A.N., Kosovec, J.E., Jobe, B.A., Turner, N.J., Zaidi, A.H., & Badylak, S.F. (2019). Extracellular Matrix Degradation Products Downregulate Neoplastic Esophageal Cell Phenotype. TISSUE ENGINEERING PART A, 25(5-6), 487-498.Mary Ann Liebert Inc. doi: 10.1089/ten.tea.2018.0105.

van der Merwe, Y., Faust, A.E., Sakalli, E.T., Westrick, C.C., Hussey, G., Chan, K.C., Conner, I.P., Fu, V.L.N., Badylak, S.F., & Steketee, M.B. (2019). Matrix-bound nanovesicles prevent ischemia-induced retinal ganglion cell axon degeneration and death and preserve visual function (vol 9, 3482, 2019). SCIENTIFIC REPORTS, 9(1), 15799.Springer Science and Business Media LLC. doi: 10.1038/s41598-019-50829-2.

van der Merwe, Y., Faust, A.E., Sakalli, E.T., Westrick, C.C., Hussey, G., Conner, I.P., Fu, V.L.N., Badylak, S.F., & Steketee, M.B. (2019). Matrix-bound nanovesicles prevent ischemia-induced retinal ganglion cell axon degeneration and death and preserve visual function. SCIENTIFIC REPORTS, 9(1), 3482.Springer Science and Business Media LLC. doi: 10.1038/s41598-019-39861-4.

Dziki, J.L., Hussey, G., & Badylak, S.F. (2018). Alarmins of the extracellular space. SEMINARS IN IMMUNOLOGY, 38(C), 33-39.Elsevier BV. doi: 10.1016/j.smim.2018.08.004.

Hussey, G.S., Cramer, M.C., & Badylak, S.F. (2018). Extracellular Matrix Bioscaffolds for Building Gastrointestinal Tissue. CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 5(1), 1-13.Elsevier BV. doi: 10.1016/j.jcmgh.2017.09.004.

Hussey, G.S., Dziki, J.L., & Badylak, S.F. (2018). Extracellular matrix-based materials for regenerative medicine. NATURE REVIEWS MATERIALS, 3(7), 159-173.Springer Science and Business Media LLC. doi: 10.1038/s41578-018-0023-x.

Ansa-Addo, E.A., Zhang, Y., Yang, Y., Hussey, G.S., Howley, B.V., Salem, M., Riesenberg, B., Sun, S., Rockey, D.C., Karvar, S., Howe, P.H., Liu, B., & Li, Z. (2017). Membrane-organizing protein moesin controls Treg differentiation and antitumor immunity via TGF-β signaling. JOURNAL OF CLINICAL INVESTIGATION, 127(4), 1321-1337.American Society for Clinical Investigation. doi: 10.1172/JCI89281.

Faust, A., Kandakatla, A., van der Merwe, Y., Ren, T., Huleihel, L., Hussey, G., Naranjo, J.D., Johnson, S., Badylak, S., & Steketee, M. (2017). Urinary bladder extracellular matrix hydrogels and matrix-bound vesicles differentially regulate central nervous system neuron viability and axon growth and branching. JOURNAL OF BIOMATERIALS APPLICATIONS, 31(9), 1277-1295.SAGE Publications. doi: 10.1177/0885328217698062.

Hussey, G.S., Keane, T.J., & Badylak, S.F. (2017). The extracellular matrix of the gastrointestinal tract: a regenerative medicine platform. NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 14(9), 540-552.Springer Science and Business Media LLC. doi: 10.1038/nrgastro.2017.76.

Gupta, S., Hau, A.M., Al-Ahmadie, H.A., Harwalkar, J., Shoskes, A.C., Elson, P., Beach, J.R., Hussey, G.S., Schiemann, W.P., Egelhoff, T.T., Howe, P.H., & Hansel, D.E. (2016). Transforming Growth Factor-β Is an Upstream Regulator of Mammalian Target of Rapamycin Complex 2-Dependent Bladder Cancer Cell Migration and Invasion. AMERICAN JOURNAL OF PATHOLOGY, 186(5), 1351-1360.Elsevier BV. doi: 10.1016/j.ajpath.2016.01.008.

Howley, B.V., Hussey, G.S., Link, L.A., & Howe, P.H. (2016). Translational regulation of inhibin βA by TGFβ via the RNA-binding protein hnRNP E1 enhances the invasiveness of epithelial-to-mesenchymal transitioned cells. ONCOGENE, 35(13), 1725-1735.Springer Science and Business Media LLC. doi: 10.1038/onc.2015.238.

Huleihel, L., Hussey, G.S., Naranjo, J.D., Zhang, L., Dziki, J.L., Turner, N.J., Stolz, D.B., & Badylak, S.F. (2016). Matrix-bound nanovesicles within ECM bioscaffolds. SCIENCE ADVANCES, 2(6), e1600502.American Association for the Advancement of Science (AAAS). doi: 10.1126/sciadv.1600502.

Link, L.A., Howley, B.V., Hussey, G.S., & Howe, P.H. (2016). PCBP1/HNRNPE1 Protects Chromosomal Integrity by Translational Regulation of CDC27. MOLECULAR CANCER RESEARCH, 14(7), 634-646.American Association for Cancer Research (AACR). doi: 10.1158/1541-7786.MCR-16-0018.

Loneker, A.E., Faulk, D.M., Hussey, G.S., D'Amore, A., & Badylak, S.F. (2016). Solubilized liver extracellular matrix maintains primary rat hepatocyte phenotype in-vitro (vol 104A, pg 957, 2016). JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 104(7), 1846.Wiley. doi: 10.1002/jbm.a.35778.

Loneker, A.E., Faulk, D.M., Hussey, G.S., D'Amore, A., & Badylak, S.F. (2016). Solubilized liver extracellular matrix maintains primary rat hepatocyte phenotype in-vitro. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 104(4), 957-965.Wiley. doi: 10.1002/jbm.a.35636.

Hussey, G.S., Howley, B.V., & Howe, P.H. (2015). Post-transcriptional mapping reveals critical regulators of metastasis. Oncoscience, 2(10), 831-832.Impact Journals, LLC. doi: 10.18632/oncoscience.207.

Hussey, G.S., Link, L.A., Brown, A.S., Howley, B.V., Chaudhury, A., & Howe, P.H. (2012). Establishment of a TGFβ-Induced Post-Transcriptional EMT Gene Signature. PLOS ONE, 7(12), e52624.Public Library of Science (PLoS). doi: 10.1371/journal.pone.0052624.

Beach, J.R., Hussey, G.S., Miller, T.E., Chaudhury, A., Patel, P., Monslow, J., Zheng, Q., Keri, R.A., Reizes, O., Bresnick, A.R., Howe, P.H., & Egelhoff, T.T. (2011). Myosin II isoform switching mediates invasiveness after TGF-β-induced epithelial-mesenchymal transition. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 108(44), 17991-17996.Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1106499108.

Chaudhury, A., Hussey, G.S., & Howe, P.H. (2011). 3′-UTR-mediated post-transcriptional regulation of cancer metastasis. RNA BIOLOGY, 8(4), 595-599.Informa UK Limited. doi: 10.4161/rna.8.4.16018.

Chaudhury, A., Hussey, G.S., & Howe, P.H. (2011). 3′-UTR-mediated post-transcriptional regulation of cancer metastasis: Beginning at the end. RNA Biology, 8(4).

Hussey, G.S., Chaudhury, A., Dawson, A.E., Lindner, D.J., Knudsen, C.R., Wilce, M.C.J., Merrick, W.C., & Howe, P.H. (2011). Identification of an mRNP Complex Regulating Tumorigenesis at the Translational Elongation Step. MOLECULAR CELL, 41(4), 419-431.Elsevier BV. doi: 10.1016/j.molcel.2011.02.003.

Chaudhury, A., Hussey, G.S., Ray, P.S., Jin, G., Fox, P.L., & Howe, P.H. (2010). TGF-β-mediated phosphorylation of hnRNP E1 induces EMT via transcript-selective translational induction of Dab2 and ILEI. NATURE CELL BIOLOGY, 12(3), 286-U94.Springer Science and Business Media LLC. doi: 10.1038/ncb2029.

Crum, R.J., Hall, K., Molina, C.P., Hussey, G.S., Graham, E., Li, H., & Badylak, S.F. (2022). Matrix Bound Nanovesicles As A Novel Extracellular Matrix Therapy For The Treatment Of Rheumatoid Arthritis. In TISSUE ENGINEERING PART A, 28, (pp. 6-7).

Hall, K.T., Fisher, S., Hussey, G.S., & Badylak, S.F. (2022). Therapeutic Potential Of Matrix Bound Nanovesicles In Rodent Model Of Ulcerative Colitis. In TISSUE ENGINEERING PART A, 28, (pp. 28-29).

Hussey, G.S., & Badylak, S.F. (2022). MATRIX BOUND NANOVESICLES: THE NEXT GENERATION OF ECM-BASED MATERIALS. In TISSUE ENGINEERING PART A, 28, (pp. S146-S147).

Hussey, G.S., & Badylak, S.F. (2022). DEVELOPMENT OF FABRICATION METHODS FOR LARGE-SCALE MANUFACTURING OF CLINICAL GRADE ECM HYDROGELS. In TISSUE ENGINEERING PART A, 28, (p. S152).

Li, J., Al Matour, B., Sato, T., Badylak, S.F., Hussey, G.S., Scott, M.J., & Arteel, G.E. (2022). THERAPEUTIC MATRIX-BOUND NANOVESICLES (MBV) PROTECT AGAINST EXPERIMENT ALCOHOL-ASSOCIATED LIVER DISEASE IN MICE. In HEPATOLOGY, 76, (pp. S983-S984).

Turner, N.J., Quijano, L.M., Hussey, G.S., Jiang, P., Badylak, S.F., Badylak, S.F. (2022). Compositional Analysis Confirms Matrix Bound Nanovesicles Have Tissue Specific Characteristics Suggesting A Regulatory Role In Homeostasis. In TISSUE ENGINEERING PART A, 28, (pp. 195-196).

Al Matour, B., Sato, T., Li, J., Merchant, M.L., Wilkey, D., Badylak, S.F., Hussey, G.S., Arteel, G.E., & Scott, M.J. (2021). EXPERIMENTAL ALCOHOL EXPOSURE ALTERS MATRIX-BOUND VESICLE CARGO AND MACROPHAGE ACTIVATION. In HEPATOLOGY, 74, (pp. 212A-213A).

Sato, T., Al Matour, B., Li, J., Merchant, M.L., Wilkey, D., Badylak, S.F., Hussey, G.S., Scott, M.J., & Arteel, G.E. (2021). EXPERIMENTAL FIBROSIS ALTERS MATRIX-BOUND VESICLES CARGO THAT DO NOT REVERT AFTER HISTOLOGIC RECOVERY. In HEPATOLOGY, 74, (pp. 813A-814A).

Zhang, Z., Liu, Q., Li, T., Hussey, G.S., Velayutham, M., Dziki, J.L., Mathews, L.R., Lee, Y.C., Dwyer, G.K., Dai, H., Roessing, A.S., Shiva, S., Oberbarnscheidt, M.H., Badylak, S.F., & Turnquist, H.R. (2019). Local IL-33 Regulates Heart Transplant Infiltrating Myeloid Cells Metabolism and Differentiation to Protect against Chronic Rejection. In AMERICAN JOURNAL OF TRANSPLANTATION, 19, (p. 526).

Hussey, G.S., & Badylak, S.F. (2017). Nanovesicles within ECM Bioscaffolds as Regulators of the Strength of Soft Tissue Repair. In TISSUE ENGINEERING PART A, 23, (p. S15).

Hussey, G.S., Dziki, J.L., Turnquist, H.R., & Badylak, S.F. (2017). Il-33 As a Key Signaling Molecule for the Therapeutic Effects of ECM Bioscaffolds for Cardiac Repair. In TISSUE ENGINEERING PART A, 23, (p. S29).

Molina, C.P., Hussey, G.S., Dziki, J.L., Eriksson, J., & Badylak, S.F. (2017). Antimicrobial Peptides with Biologic and Biosynthetic Scaffolds for Regenerative Medicine. In TISSUE ENGINEERING PART A, 23, (pp. S28-S29).

Torres, C.M., Reing, J.E., Molina, C.P., Hussey, G.S., & Badylak, S.F. (2017). Tissue-Specific Extracellular Matrix Hydrogel Promotes the Growth and Differentiation of Lgr5+Intestinal Stem Cells into Viable Enteroids. In JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 225(4), (p. S204).Ovid Technologies (Wolters Kluwer Health). doi: 10.1016/j.jamcollsurg.2017.07.470.

Molina, C.P., Giglio, R.M., Hussey, G.S., Sicari, B.M., Gandhi, R.M., & Badylak, S.F. (2016). Expression of Antimicrobial Peptides by Macrophages Exposed to Solubilized Extracellular Matrix. In TISSUE ENGINEERING PART A, 22, (p. S98).