Santhakumar Manicassamy

ORCID: 0000-0002-2203-3917
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About
Contact & Profiles
Research Areas
  • Immunotherapy and Immune Responses
  • Immune Cell Function and Interaction
  • Immune Response and Inflammation
  • T-cell and B-cell Immunology
  • Epigenetics and DNA Methylation
  • Wnt/β-catenin signaling in development and cancer
  • interferon and immune responses
  • Helicobacter pylori-related gastroenterology studies
  • Histone Deacetylase Inhibitors Research
  • Retinoids in leukemia and cellular processes
  • RNA modifications and cancer
  • Galectins and Cancer Biology
  • Cancer Cells and Metastasis
  • Colorectal Cancer Treatments and Studies
  • DNA Repair Mechanisms
  • Ubiquitin and proteasome pathways
  • Cancer Immunotherapy and Biomarkers
  • Influenza Virus Research Studies
  • Signaling Pathways in Disease
  • NF-κB Signaling Pathways
  • Cancer-related gene regulation
  • Immune cells in cancer
  • Digestive system and related health
  • Cancer Genomics and Diagnostics
  • Peptidase Inhibition and Analysis

Augusta University
2013-2025

Augusta University Health
2016-2025

Georgia Regents Medical Center
2013-2016

Cancer Research Center
2014

Emory University
2009-2011

Emory National Primate Research Center
2008-2011

Emory Healthcare
2008-2010

University of Illinois Chicago
2005-2009

University of Illinois Urbana-Champaign
2005-2008

University of Chicago Medical Center
2008

Dendritic cells (DCs) play a vital role in initiating robust immunity against pathogens as well maintaining immunological tolerance to self antigens. However, the intracellular signaling networks that program DCs become tolerogenic remain unknown. We report here Wnt-beta-catenin intestinal dendritic regulates balance between inflammatory versus regulatory responses gut. beta-catenin was required for expression of anti-inflammatory mediators such retinoic acid-metabolizing enzymes,...

10.1126/science.1188510 article EN Science 2010-08-12

Influenza A virus is being extensively studied because of its major impact on human and animal health. However, the dynamics influenza infection cell types infected in vivo are poorly understood. These characteristics challenging to determine, partly there no efficient replication-competent expressing an easily traceable reporter gene. Here, we report generation a recombinant carrying GFP gene NS segment (NS1-GFP virus). Although attenuated when compared with wild-type virus, NS1-GFP...

10.1073/pnas.0914994107 article EN Proceedings of the National Academy of Sciences 2010-06-07

Although several subsets of intestinal APCs have been described, there has no systematic evaluation their phenotypes, functions, and regional localization to date. In this article, we used 10-color flow cytometry define the major APC in small large intestine lamina propria. Lamina propria could be subdivided into CD11c(+)CD11b(-), CD11c(+)CD11b(+), CD11c(dull)CD11b(+) subsets. CD11c(+)CD11b(-) cells were largely CD103(+)F4/80(-) dendritic (DCs), whereas CD11c(+)CD11b(+) subset comprised...

10.4049/jimmunol.1002701 article EN The Journal of Immunology 2011-06-11

Mammary stem/progenitor cells (MaSCs) maintain self-renewal of the mammary epithelium during puberty and pregnancy. DNA methylation provides a potential epigenetic mechanism for maintaining cellular memory self-renewal. Although methyltransferases (DNMTs) are dispensable embryonic stem cell maintenance, their role in MaSCs cancer (CSCs) constantly replenishing is unclear. Here we show that DNMT1 indispensable MaSC maintenance. Furthermore, find expression elevated tumours, gland-specific...

10.1038/ncomms7910 article EN cc-by Nature Communications 2015-04-24

Recently, impressive technical advancements have been made in the isolation and validation of mammary stem cells cancer (CSC), but signaling pathways that regulate cell self-renewal are largely unknown. Furthermore, CSCs believed to contribute chemo- radioresistance. In this study, we used MMTV-Neu-Tg mouse tumor model identify potential new strategies for eliminating CSCs. We found both luminal progenitor basal susceptible genetic epigenetic modifications, which facilitate oncogenic...

10.1158/0008-5472.can-15-2249 article EN Cancer Research 2016-04-06

Abstract At mucosal sites such as the intestine, immune system launches robust immunity against invading pathogens while maintaining a state of tolerance to commensal flora and ingested food Ags. The molecular mechanisms underlying this phenomenon remain poorly understood. In study, we report that signaling by GPR81, receptor for lactate, in colonic dendritic cells macrophages plays an important role suppressing inflammation restoring homeostasis. Genetic deletion GPR81 mice led increased...

10.4049/jimmunol.1700604 article EN The Journal of Immunology 2018-01-31

Breakdown in immunological tolerance to self-Ags or uncontrolled inflammation results autoimmune disorders. Dendritic cells (DCs) play an important role regulating the balance between inflammatory and regulatory responses periphery. However, factors tissue microenvironment signaling networks critical for programming DCs control chronic promote are unknown. In this study, we show that wnt ligand-mediated activation of β-catenin is promoting limiting neuroinflammation. DC-specific deletion key...

10.4049/jimmunol.1402691 article EN The Journal of Immunology 2015-02-26

Tumors actively suppress antitumor immunity, creating formidable barriers to successful cancer immunotherapy. The molecular mechanisms underlying tumor-induced immune tolerance are largely unknown. In the present study, we show that dendritic cells (DC) in tumor microenvironment acquire ability metabolize vitamin A produce retinoic acid (RA), which drives regulatory T-cell responses and tolerance. Tolerogenic were dependent on induction of A-metabolizing enzymes via β-catenin/T-cell factor...

10.1158/0008-5472.can-14-2377 article EN Cancer Research 2015-01-08

Organ cross talk exists in many diseases of the human and animal models diseases. A recent study demonstrated that inflammatory mediators can cause acute kidney injury neutrophil infiltration a mouse model dextran sodium sulfate (DSS)-colitis. However, chemokines their receptors may mediate distant organ effects colitis are unknown. We hypothesized keratinocyte chemoattractant (KC)/IL-8 receptor chemokine (C-X-C motif) ligand 2 (CXCL2) mediates DSS-colitis-induced injury. Consistent with our...

10.1152/ajprenal.00319.2013 article EN AJP Renal Physiology 2013-08-29

Abstract Dendritic cells (DCs) sense microbes via multiple innate receptors. Signals from different receptors are coordinated and integrated by DCs to generate specific adaptive immune responses against pathogens. Previously, we have shown that two pathogen recognition receptors, TLR2 dectin-1, which recognize the same microbial stimulus (zymosan) on DCs, induce mutually antagonistic regulatory or inflammatory responses, respectively. How diametric signals these in regulate incite immunity...

10.4049/jimmunol.1400614 article EN The Journal of Immunology 2014-09-11

Abstract Dietary lipids and their metabolites activate members of the peroxisome proliferative–activated receptor (PPAR) family transcription factors are critical for colonic health. The PPARα isoform plays a vital role in regulating inflammation various disease settings, but its intestinal inflammation, commensal homeostasis, mucosal immunity gut unclear. In this study, we demonstrate that pathway innate immune cells orchestrates homeostasis by expression IL-22 antimicrobial peptides...

10.4049/jimmunol.1501489 article EN The Journal of Immunology 2016-04-26

Retinoic acid inducible gene-I (RIG-I) is an innate RNA sensor that recognizes the influenza A virus (IAV) genome and activates antiviral host responses. Here, we demonstrate RIG-I signaling plays a crucial role in restricting IAV tropism regulating immune Mice deficient RIG-I-MAVS pathway show defects migratory dendritic cell (DC) activation, viral antigen presentation, priming of CD8+ CD4+ T responses during infection. These result decreased frequency polyfunctional effector cells lowered...

10.1371/journal.ppat.1005754 article EN cc-by PLoS Pathogens 2016-07-20

Macroautophagy/autophagy contributes to maladaptive kidney repair by inducing pro-fibrotic factors such as FGF2 (fibroblast growth factor 2), but the underlying mechanism remains elusive. Here, we show that EGR1 (early response 1) was induced in injured proximal tubules after ischemic acute injury (AKI) and this induction suppressed autophagy deficiency inducible, renal tubule-specific atg7 (autophagy related 7) knockout (iRT-atg7 KO) mice. In cultured tubular cells, TGFB1 (transforming beta...

10.1080/15548627.2023.2281156 article EN Autophagy 2023-11-18
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