# Glycogen Synthase Kinase 3 beta in liver ischemia reperfusion injury > **NIH NIH R01** · UNIVERSITY OF CALIFORNIA LOS ANGELES · 2022 · $351,000 ## Abstract Project Summary Ischemia reperfusion injury (IRI) is a major complication after liver surgery. In liver transplantation, it is a major risk factor for both acute and chronic graft rejection and restrains the use of marginal donors. Liver inflammatory immune response drives the pathogenesis of IRI. Despite the progress in studies of cellular and molecular mechanisms of the response, questions regarding to the potential distinctive roles of tissue resident vs. infiltration macrophages (iMФs), and the resolution of liver IRI remain to be defined. Glycogen synthase kinase 3β (Gsk3β) is a unique signaling kinase that it differentially regulates pro- and anti-inflammatory gene programs in MФs upon innate stimulations. It has been shown in a murine liver partial warm ischemia model that both Gsk3 inhibitors in WT hosts and myeloid Gsk3β deficiency protect livers from IRI via an AMPK- IL-10-dependent mechanism. The clinical relevance of AMPK in liver ischemia has been documented recently in hepatic tumor resection. Preliminary experiments of this proposal have found that Gsk3β also regulates the resolution of liver IRI. In fact, Gsk3β regulates liver inflammatory immune activation and resolution by targeting distinctive populations of liver MФs. KCs depletion diminished the liver protective phenotype in myeloid Gsk3β KO mice against IR. However, the recovery of liver IRI remain accelerated in these KC-depleted KO hosts, indicating that Gsk3β regulates iMФs in resolving tissue inflammation. Current proposal will dissect mechanisms of Gsk3β regulation of these two types of MФs at different stages of liver IRI. IR-induced liver inflammatory immune activation is characterized by infiltration and activation of MФs from peripheral (iMՓs), as well as necroptotic depletion and pro-inflammatory conversion of tissue resident KCs. In liver inflammation resolution, MФs repair hepatocellular damage and clear infiltrated neutrophils via Tyro3-Axl-MerTK (TAM) receptor tyrosine kinase (RTK)-mediated efferocytosis. Macrophage necroptosis and efferocytosis potently regulate their activation and differentiation. Gsk3β promotes stress-induced cell death and regulates TAM expressions in MФs. The proposal will test the hypothesis that Gsk3β regulates KC necroptosis via AMPK and pro-inflammatory immune activation via Mer RTK; and Gsk3β inhibition/inactivation facilitates iMФ conversion from pro-inflammatory to reparative type by enhancing Axl-mediated efferocytosis and immune regulatory signaling. Two specific aims are designed to address how Gsk3β regulates KC inflammatory activation, and iMФ reprogramming/functions, in the activation and resolution stages of liver IRI, respectively. Results of these experiments shall offer fresh new insight into immune regulatory functions of Gsk3β in MФs in both the activation and resolution of liver inflammation and injuries and provide rationales for novel therapeutic strategies to restore liver homeostasis in patients. ## Key facts - **NIH application ID:** 10348751 - **Project number:** 5R01DK119338-03 - **Recipient organization:** UNIVERSITY OF CALIFORNIA LOS ANGELES - **Principal Investigator:** YUAN ZHAI - **Activity code:** R01 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2022 - **Award amount:** $351,000 - **Award type:** 5 - **Project period:** 2020-05-01 → 2023-02-28 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10348751 ## Citation > US National Institutes of Health, RePORTER application 10348751, Glycogen Synthase Kinase 3 beta in liver ischemia reperfusion injury (5R01DK119338-03). Retrieved via AI Analytics 2026-05-21 from https://api.ai-analytics.org/grant/nih/10348751. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*