Match tier Institution-verified
Presence Current · Arkansas
Last published 2026
Sources Institutional record
Refreshed 2026-10-08

Shengyu Mu

Sourced from institutional research profiles (UAMS TRI or ARA).

Federal Grant PI

Professor and Department Chair

Also affiliated: University of Arkansas Medical Center (2022–2025); University of Tokyo Hospital (2012); The University of Tokyo (2009–2015)

18 h-index 97 pubs 1,472 cited

  • Animals
  • Hypertension
  • Mice
  • Humans
  • Male
  • Disease Models, Animal
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Rats
  • Kidney
  • Signal Transduction
  • Reactive Oxygen Species
  • CD8-Positive T-Lymphocytes
  • Sarcoma, Kaposi
  • Herpesvirus 8, Human

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Biography and Research Information

OverviewAI-generated summary

Shengyu Mu investigates the mechanisms underlying salt-sensitive hypertension, focusing on the roles of immune cells and specific molecular pathways in the kidney. His federally funded research, supported by a $746,704 grant from the NIH/National Heart Lung and Blood Institute, examines how T cell homing to the kidney contributes to salt retention and blood pressure regulation. Mu's work has identified the Rac1 GTPase and the mineralocorticoid receptor as critical components of salt-sensitive hypertension in rodent models. He has also explored the involvement of CD8+ T cells and the Na-Cl co-transporter NCC in distal convoluted tubules, as well as the IFNγ-PDL1 pathway in promoting hypertension.

Beyond hypertension, Mu's research extends to other physiological processes. He has studied the regulation of PCSK9 secretion by the NLRP3 inflammasome via IL-1β and by blood flow patterns mediated by MyD88-dependent pro-inflammatory cytokines. Additionally, his work has investigated the impact of high-salt and high-fat diets on inflammation and fibrosis in mouse models of liver steatosis, and the acceleration of vascular calcification by fibroblast growth factor 23 in the absence of Klotho deficiency.

Mu's scholarly output includes 106 publications and an h-index of 18, with over 1,500 citations. He actively collaborates with researchers at the University of Arkansas for Medical Sciences, including Yunmeng Liu, Christoph Mora, Katherine Deck, and Yunping Guo, with whom he shares numerous publications.

Metrics

  • h-index: 18
  • Publications: 97
  • Citations: 1,472

Positions

  • University of Arkansas for Medical Sciences publications 2016–2026
    ORCID
  • Professor and Department Chair publications 2016–2026
    University of Arkansas for Medical Sciences Institution web page

Selected Publications

  • Macrophage Plasticity Drives Cardiac Dysfunction in Hypertension 2253031 (2026)
    The Journal of Immunology DOI OpenAlex
  • Antigen-independent formation of renal Trm-like CD8 T cells perpetuates hypertension 2259853 (2026)
    The Journal of Immunology DOI OpenAlex
  • Targeting BRD2 and BRD4 inhibit the growth of KSHV-infected immortalized endothelial cells through suppression of LANA translation (2026)
    PLoS Pathogens DOI OpenAlex
  • Targeting Hyaluronan Signaling Overcomes Primary Effusion Lymphoma Cells Resistance to Rapamycin (2026)
    Biological Procedures Online DOI OpenAlex
  • Kidney Resident Memory CD8+ T cells drive the immortality of hypertension (2026)
    Physiology DOI OpenAlex
  • Cytokine-mediated macrophage transition promotes early cardiac fibrosis in chronic hypertension (2026)
    Physiology DOI OpenAlex
  • CD5L promotes efferocytosis and resolution of retinal ischemic injury (2026)
    Cell Death and Disease DOI OpenAlex
  • Nanoencapsulated gamma-oryzanol enhances fibroblast proliferation, migration, and reduces oxidative stress in H2O2-induced cellular aging model (2025)
    Journal of Functional Foods DOI OpenAlex
  • IL-10 Drives Macrophage to Myofibroblast Transition Promoting Chronic Fibrosis in the Failing Heart 9287 (2025)
    The Journal of Immunology DOI OpenAlex
  • P2X7 Drives T-cell Activation Promoting Chronic Inflammation During High Blood Pressure 9289 (2025)
    The Journal of Immunology DOI OpenAlex
  • Kidney resident-memory CD8+ T cells drive chronic high blood pressure 9288 (2025)
    The Journal of Immunology DOI OpenAlex
  • Kidney Memory for Salt Sensitivity Resides in T Cells Driving Chronic Hypertension (2025)
    Journal of the American Society of Nephrology DOI OpenAlex
  • Uncovering immune pathways for therapeutic targeting of hypertension (2025)
    Expert Opinion on Therapeutic Targets 1 citation DOI OpenAlex
  • Immune Dysregulation Connecting Type 2 Diabetes and Cardiovascular Complications (2025)
    Life 2 citations DOI OpenAlex
  • Cytokine-induced Macrophage Transition Drives Cardiac Fibrosis and Diastolic Dysfunction (2025)
    Physiology DOI OpenAlex

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Federal Grants 1 $746,704 total

NIH Contact PI Apr 2019 - Mar 2029

T cell homing to the kidney contributes to salt retention and blood pressure regulation

National Heart Lung and Blood Institute $746,704 R01

Grants & Funding

As listed on this researcher's institutional profile. Federal awards with verified records are shown above.

  • AHA Pre-doc Fellowship Deck American Heart Association
  • T cell homing to the kidney contributes to salt retention and blood pressure regulation - Continuation NIH/Nat. Heart, Lung & Blood Institute
  • Mu Lab Funding UAMS College of Medicine
  • Role of Immune Cells in kidney in the Development of Salt-Sensitive Hypertension (Funded by: American Heart Association (SouthWest Affiliate))
  • Determination of antihypertensive, anti-inflammatory and chymase inhibitory efficacy of sweet potato and rice bran extract US Department of Agriculture via University of Arkansas at Pine Bluff
  • Kidney-resident memory CD8+ T cells promote hypertension and memorize salt sensitivity. NIH/Nat. Heart, Lung & Blood Institute
  • Formation of CD8Trms in the kidney contributes to salt-memory of hypertension American Heart Association
  • Center for Studies of Host Response to Cancer Therapy NIH

Collaboration Network

153 Collaborators 49 Institutions 5 Countries

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