Lonnie Shea
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About
The Shea Lab works at the interface of regenerative medicine, biomaterials, and systems biology. The central theme for the various projects is creating synthetic environments which can be employed to molecularly dissect tissue formation, promote tissue regeneration or function, and monitor disease initiation or progression.
Links
https://shearesearch.engin.umich.edu/
Qualifications
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Postdoctoral FellowUniversity of Michigan, School of Dentistry, USA
Postdoctoral Fellowship
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PhDUniversity of Michigan, USA
Center Memberships
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Center MemberAI and Digital Health Innovation
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Center MemberCenter for Cell Plasticity and Organ Design
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Center MemberBiointerfaces Institute
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Center MemberRogel Cancer Center
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Center MemberBiosciences Initiative
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Center MemberRegenerative Medicine Resource Center
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Center MemberCaswell Diabetes Institute
Research Overview
Of particular emphasis in the lab is:
Applying the controllable microenvironments to in vitro and in vivo models of tissue formation, including nerve regeneration, and islet formation and function.
Engineering nanoparticles or environments to modulate innate and adaptive immune responses for autoimmune and allergic disease, responses to trauma, and to prevent rejection of transplanted cells or tissue.
Developing diagnostic systems for cancer, autoimmune disease, and transplant rejection that can detect immune dysregulation associated with disease onset, and monitor for the response to therapy.
Recent Publications
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King JL, Spencer C, Youngblood R, Crumley K, Bealer E, Rios PD, Joshi I, Ghani S, Isa D, McGarrigle JJ, Cook D, Locke C, Abraham A, Clark A, Oberholzer J, Shea LD. Biotechnology and Bioengineering, 2026 Mar 1; 123 (3): 742 - 751.Journal ArticleGamma Irradiation of Poly(lactide-co-glycolide) Scaffolds Reduces the Mechanical Stability and Function of Islet Grafts in Diabetic Nonhuman Primates
DOI:10.1002/bit.70134 PMID: 41439800 -
Nekanti U, Sakthivel PS, Nishi RA, Anzalone A, Dumont CM, Bin Lee J, McDonald S, Song H, Obenaus A, Gershon PD, Bradke F, Shea LD, Cummings BJ, Anderson AJ. 2026 Feb 11; bioRxiv,PreprintMicrotubule Stabilization and Biomaterial Guidance Synergize to Enhance CST Regeneration and Motor Recovery After Chronic SCI
DOI:10.64898/2026.02.05.703927 -
King JL, Roy J, Urie RR, Bealer E, Crumley K, Rad L, Soleimanpour SA, Shea LD. Science Advances, 2026 Jan 28; 12 (5):Journal ArticleLongitudinal monitoring of type 1 diabetes progression to disease onset
DOI:10.1126/sciadv.adw8946 PMID: 41604487 -
Pereles RS, Roy J, Brooks MD, Wicha MS, Jeruss JS, Shea LD, Orbach SM. Biotechnol Bioeng, 2026 Jan 10;Journal ArticleDynamic Immune Cell Composition, Phenotypes, and Signaling in an Engineered Metastatic Niche.
DOI:10.1002/bit.70140 PMID: 41518488 -
Podojil JR, Cogswell AC, Neef T, Chiang MY, Beddow SA, Arellano G, Kakade S, McCarthy DP, Elhofy A, Harp CT, Khan M, Meeks JJ, Xu D, Shea LD, Miller SD. Science Advances, 2026 Jan 2; 12 (1): eadv8860Journal ArticleSTING/type I interferon pathway is required for antigen-containing PLGA nanoparticle- and apoptotic cell-induced CD4+ T cell tolerance
DOI:10.1126/sciadv.adv8860 PMID: 41481727 -
Ma JA, Griffin KV, Kang K, Diener A, Schrack IA, Bealer EJ, Rad LM, Pereles RS, Jeruss JS, Shea LD. Cell Biomaterials, 2026 Jan 1;Journal ArticleNanoparticle induction of antigen-presenting monocyte-derived dendritic cells relieves immunosuppression and inhibits metastasis
DOI:10.1016/j.celbio.2025.100343 -
Viola H, Carter H, Griffin K, Costa RM, McDonald R, Callow B, de Los Santos FG, Martinez M, Chen R, Hunter Z, Luker G, Moore BB, Shea L. bioRxiv, 2025 Dec 24;Journal Article"Immunomodulatory nanoparticles elicit antifibrotic monocyte activation to resolve murine pulmonary fibrosis".
DOI:10.64898/2025.12.22.696047 PMID: PMC12776067 -
Lietzke AC, Walker EM, Bealer E, Crumley K, King J, Stendahl AM, Zhu J, Pearson GL, Levi-D’Ancona E, Henry-Kanarek B, Davidson RK, Li J, Reck EC, Wu Y, Arnipalli M, Pham JP, Mundada L, Sidarala V, Herron TJ, Coronel MM, Pennathur S, Madsen JGS, Shea LD, Soleimanpour SA. Nature Communications, 2025 Dec 1; 16 (1):Journal ArticleLimitations in PPARα-dependent mitochondrial programming restrain the differentiation of human stem cell-derived β cells
DOI:10.1038/s41467-025-66022-1 PMID: 41372150
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