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  • Raghavan Pillai Raju, PhD

Raghavan Pillai Raju, PhD

Dr. Raju

 

Professor Pharmacology & Toxicology

Carl Sanders Research & Education Building, CB260
rraju@augusta.edu
 
Office: 706-443-4138
Lab: 706-446-0019
 

Members of the Lab

photo of Lun Cai, PhD

Lun Cai, PhD

  • Postdoctoral Fellow

lcai@augusta.edu

photo of Parmita Kar, PhD

Parmita Kar, PhD

  • Postdoctoral Fellow

pkar@augusta.edu

photo of Rupa Lavarti, PhD

Rupa Lavarti, PhD

  • Research Associate

rlavarti@augusta.edu

photo of Swetha Mundanattu, PhD

Swetha Mundanattu, PhD

  • Postdoctoral Fellow

SMUNDANATTU@augusta.edu

photo of Bhavishya Mundluru

Bhavishya Mundluru

  • Graduate Student

BMUNDLURU@augusta.edu

 

Research Interest

Dr. Raju’s research is focused on immuno-metabolic alterations in injury and aging. His laboratory uses a multidisciplinary approach to investigate the molecular basis of organ function changes following injury and the influence of aging. His current research intersects areas in inflammation, aging, mitochondrial biology, and metabolism. The following are some of the projects that are ongoing in Dr. Raju’s laboratory.

Mitochondrial function in aging and injury.

In this project, Dr. Raju’s laboratory investigates metabolic pathways converging on mitochondria and mitochondrial functional alterations following hemorrhagic shock and sepsis. He found that activation of Sirt1 improves organ function and survival following hemorrhagic shock. His continued studies showed that the NAD (Sirt1 co-substrate) precursor niacin also improved survival following hemorrhagic shock, and his lab dissected the roles of the niacin receptor (GPR109a) and NAD in niacin-mediated salutary effect (BBA Mol Bas Dis, 2019). Further studies directly targeting mitochondria (dichloroacetate) established that improving mitochondrial function following acute injury can improve organ function and survival. While mitochondria can exacerbate inflammation by releasing damage-associated molecular patterns, they can also negatively control inflammation.   Dr. Raju’s laboratory continues investigations into the alterations in mitochondria-centered pathways to develop novel treatment strategies (Metabolism, 2022; Free Radic Biol Med., 2022).

Acute injury-induced senescence.

Senescence plays a critical role in several biological processes and conditions, including cancer, aging, injury, and development. Dr. Raju’s recent studies show the emergence of a senescent-like cellular phenotype following hemorrhagic shock as well as sepsis, and the function of these cells is likely context-dependent. His laboratory is further investigating the functional role of these cells and the effect of senolytics in the context of aging and injury (Aging Cell, 2020; Npj Aging, 2024; Aging Cell, 2024, PMID: 39444093).

Extracellular vesicles in long-distance communication:

Dr. Raju’s laboratory has recently observed that young animals are more resilient to injury than mature or old animals. Subsequent studies from his laboratory demonstrated that circulating extracellular vesicles (EVs) from young mice have protective effects in old mice. One of his funded projects is focused on the mechanistic basis of plasma EV-induced protection in older animals (Aging Dis. 2022; Aging, 2023; Journal of Extracellular Vesicles, in press, 2025).

Dr. Raju collaborates with other investigators locally within the Medical College of Georgia, nationally, and internationally. His research and experience encompass areas in Biochemistry, Physiology, Immunology, Molecular Biology, Pharmacology, and Cell biology. Dr. Raju has authored over 90 peer-reviewed articles. His research is supported by grants from the National Institutes of Health, the United States Department of Veterans Affairs, and the Department of Defense.

Education & Post-Doctoral Training

2000

Research Associate
Mayo Clinic, Rochester, MN

1995

Postoctoral Training
University of Minnesota, St Paul, MN

1993

PhD
All India Institute of Medical Sciences, New Delhi

Academic Appointments

2013 - Present    Professor, Augusta University, Augusta, GA

2007 - 2013         Associate Professor, University of Alabama at Birmingham, Birmingham, AL

2001 - 2007         Senior Staff Fellow, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD

Editorial Board

2014 - present    BBA - Molecular Basis of Disease

2013 - present    PLOS ONE, Academic Editor

2010 - present   Aging and Disease

2017                        Guest Editor: BBA Mol Basis of Dis

2014                        Guest Editor: Aging and Injury (Special Issue of Aging and Disease)

2006 - 2010         Journal of Immunology, Associate Editor

Frontiers in Intensive Care Medicine and Anesthesiology

Grant Review Panels

Dr. Raju has served on several grant review panels including study sections of the National Institutes of Health, Department of Veterans Affairs, Department of Defense, and American Heart Association. Dr. Raju has also served on an NIH study section as a Chartered member.

Selected Publications

Lavarti R, Alvarez-Diaz T, Marti K, Kar P, Raju RP.  The context-dependent effect of cellular senescence: from embryogenesis and wound healing to aging. Aging Research Reviews (accepted, in Press).

Cai L, Kar P, Liu Y, Chu X, Sharma A, Lee TJ, Arbab A, Raju RP. Plasma extracellular vesicle-derived miR-296-5p is a maturation-dependent rejuvenation factor that downregulates inflammation and improves survival after sepsis. Journal of Extracellular Vesicles 2025 Apr;14(4):e70065 article link.

Lavarti R, Cai L, Alvarez-Diaz, Rodriguez TM, Bombin S and Raju RP. Senescence landscape in the liver following sepsis and senolytics as potential therapeutics. Aging cell, 2025 Jan;24(1):e14354.  (Science News Story).

Kar P, Sivasailam A, Lavarti R, Cai L, Thangaraju M, Nguyen, E, Mundluru B and Raju RP. p53 dependence of senescence markers p21v1 and p21v2 in aging and acute injury. NPJ Aging, 2024 Oct 14;10(1):45.

Schoenmann N, Tannenbaum N, Hodgeman RM, Raju RP. Regulating mitochondrial metabolism by targeting pyruvate dehydrogenase with dichloroacetate, a metabolic messenger. Biochim Biophys Acta Mol Basis Dis. 2023 Oct;1869(7):166769.

Cai L, Arbab AS, Lee TJ, Sharma A, Thomas B, Igarashi K, Raju RP. BACH1-Hemoxygenase-1 axis regulates cellular energetics and survival following sepsis. Free Radic Biol Med. 2022 Jun 9;188:134-145.

Chu X, Raju RP. Regulation of NAD+ metabolism in aging and disease. Metabolism. 2021 Oct 28;126:154923.

Chu X, Wen J, Raju RP. Rapid senescence-like response after acute injury.  Aging Cell. 2020 Aug 2:e13201.  Science News Story.

Chu X, Schwartz R, Diamond MP and Raju R.  A combination treatment strategy for hemorrhagic shock modulates autophagy. Frontiers in Medicine. 2019;6:281.Chu X, Wu S and Raju R. NLRX1 regulation in acute mitochondrial injury. Frontiers in Immunology, 2019;10:2431.

Subramani K, Chu X, Warren M, Singh N and Raju R. Deficiency of metabolite sensing receptor HCA2 impairs the salutary effect of niacin in hemorrhagic shock BBA Mol Basis Dis. 2019; 1865(3):688-695.

Subramani K, Raju SP, Chu X, Warren M, Pandya DC, Hoda N, Fulzele S and Raju R. Effect of plasma-derived extracellular vesicles on erythrocyte deformability in polymicrobial sepsis. International Immunopharmacology 2018; 65:244-247.

McMenamin M, Kvirkvelia N, Warren M, Jadeja R, Sharma A, Raju R and Madaio MP. Kidney targeted inhibition of protein kinase C-α ameliorates nephrotoxic nephritis by restoring mitochondrial dysfunction in endothelial cells. Kidney International.2018; 94(2):280-291.

Ben H and Raju R. Mitochondria in hypoxic ischemic injury and influence of aging. Progress in Neurobiology. 2017; 157:92-116.

Kumar S, Lu S, Warren M, Chu X, Haroldo, T, Caldwell, W, Diamond M, Raju R.  Mitochondrial targeting improves survival following hemorrhagic shock.  Scientific Reports 2017: 7(1):2671.Jian B, Yang S, Chaudry IH and Raju R. Resveratrol improves cardiac contractility following trauma-hemorrhage by modulating Sirt1. Molecular Medicine 2012 18(1):209-14.

 

 Complete list of publications


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