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Overview

Research in my laboratory centers on understanding the cellular and molecular mechanisms of tissue inflammation and injury, including the kidney, lung, and vasculature, in the pathogenesis of acute and chronic diseases. Our work has focused on examining the mechanisms of signal transduction by Transforming Growth Factor-beta1 (TGF-β1), a pleiotropic cytokine and key mediator of tissue injury response and kidney fibrosis. We have extensively examined how TGF-β1 effects are mediated by the distinct TGF-β receptors via activation of intracellular signaling molecules downstream to the receptors in a cell-specific manner to regulate cellular responses in renal cells. 

Our investigations have included (1) cloning and characterization of the cell surface receptors, and identification of novel interacting proteins that are involved in TGF-β1 signal transduction, (2) delineating the downstream intracellular signal transducing pathways that mediate TGF-β1 signals, in particular, the role of the mitogen-activated protein kinase (MAPK) pathways, and (3) the cellular and molecular regulation of TGF-β1 induction of cytoprotectants, such as heme oxygenase-1 (HO-1) and carbon monoxide (CO).

We are currently investigating novel mechanisms of regulation and function of autophagy, inflammasomes, and necroptosis in models of organ injury, including the kidney, lung, and heart. In collaboration with laboratories at Weill Cornell Medical College, we are also studying mechanisms of multi organ injury in sepsis, acute and chronic lung injury (Dr. Augustine Choi, Stephen and Suzanne Weiss Dean, Weill Cornell Medicine and Professor, Division of Pulmonary & Critical Care Medicine), HIV/antiretroviral therapy related cardiac/kidney fibrosis (Dr. Jeffrey Laurence, Professor of Medicine, Division of Hematology & Medical Oncology), and juvenile chronic kidney disease (Dr. Oleh Akchurin, Assistant Professor of Pediatrics, Division of Pediatric Nephrology). The ultimate goal of our research is to identify novel therapeutic targets that will provide cytoprotection against tissue injury such as progressive kidney diseases.

Highlights

  1. 1
    Kidney international · 2022
    PMID: 35227692PMCID: PMC9038692DOISenior author42 citations
  2. 2
    Kidney360 · 2021
    PMID: 33629075PMCID: PMC7901833DOISenior author22 citations
  3. 3
    Kidney international · 2025
    PMID: 41401886DOISenior author1 citations

Publications

90 publications

Active

4 grants
  • Co-I
    QSM for detection of hemorrhaging cysts and risk stratification in ADPKD
    National Institute of Diabetes and Digestive and Kidney Diseases · 2025–2029
    R01DK139336-01A1
  • Co-I
    Gene Nutrient Interactions in Kidney Function
    National Institute of Diabetes and Digestive and Kidney Diseases · 2017–2027· 2 renewals
    R01DK113088-05
  • PI
    Distinct and Overlapping Pathways of Fibrosis and Emphysema in Cigarette Smokers
    National Heart, Lung, and Blood Institute · 2021–2027
    P01HL114501-10
  • KP
    Mitofusins modulate kidney fibrosis-associated lung injury and kidney-lung deleterious crosstalk.
    National Institute of Diabetes and Digestive and Kidney Diseases · 2025–2026 · via The Board of Trustees of the University of Alabama for the University of Alabama at Birmingham
    U24DK137318-03S1
Completed grants (11)
  • Co-I
    A Phase II Study of Inhaled CO for the Treatment of ARDS
    U.S. Department of Defense · 2018–2025
    W81XWH-18-1-0667
  • Co-I
    A Phase 1b Study of Inhaled CO for the Treatment of Sepsis-Induced ARDS
    National Heart, Lung, and Blood Institute · 2020–2025
    R61HL153011-01
  • PI
    Inflammasomes: Regulation and Function in Acute Lung Injury
    National Heart, Lung, and Blood Institute · 2013–2023· 2 renewals
    R01HL055330-23
  • PI
    Novel role of RIPK3-dependent necroptosis pathway in lung and kidney fibrosis
    National Heart, Lung, and Blood Institute · 2017–2022
    R01HL133801-04
  • Co-I
    Clinical and Translational Science Center - UL1
    National Center for Advancing Translational Sciences · 2017–2022
    UL1TR002384-01
  • Co-I
    Metabolic Dysfunction Regulates Mitophagy-Dependent Necroptosis in COPD
    National Heart, Lung, and Blood Institute · 2017–2021
    R01HL132198-01A1
  • PI
    Heme Oxygenase - 1/Carbon Monoxide in Lung Vascular Injury
    National Heart, Lung, and Blood Institute · 2014–2020
    R01HL060234-13
  • KP
    Mechanisms of HIV/ART Related Cardiac Fibrosis
    National Heart, Lung, and Blood Institute · 2014–2017
    R21HL125044-02
  • KP
    Carbon Monoxide: Novel Opportunities for Therapy-Project 1
    National Heart, Lung, and Blood Institute · 2013–2017 · via The Brigham & Women's Hospital INC
    P01HL108801-05
  • PI
    TGF-Beta Signaling in the Kidney
    National Institute of Diabetes and Digestive and Kidney Diseases · 2013–2017
    R01DK057661-14
  • PI
    Heme Oxygenase-1/Carbon Monoxide in Sepsis
    National Heart, Lung, and Blood Institute · 2014–2015
    R01HL079904-16 EW

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