Medford, Tiruchirappalli,Massachusetts, Tamil Nadu
Overview
14
14
years of post-secondary education
Work History
Associate professor
Dept of Biochemistry
Research Assistant Professor
Dr,Prabhakaran
Associate Director
University of Illinois
Chicago
60612
E-mail: praba.biopioneer@gmail.com, Research Resources Center
Bioanalytics, Biophysics, and Cytomics Division
Director,
Flow Cytometry Core Shared Resources Core Leader, UI Cancer Center
bganesh@uic.edu tel: 312-3550742, 312-996-2775
Education
Post-doctoral Research Associate - undefined
University of Illinois
01.2020 - 05.2022
Ph.D - Biochemistry
Bharathidasan University
01.2010 - 01.2016
M.Phil - Biochemistry
SASTRA University
01.2008 - 01.2009
M.Sc. - Biochemistry
SASTRA University
01.2006 - 01.2008
B. Sc. - Biochemistry
Mother Teresa University
01.2003 - 01.2006
Accomplishments
University of Illinois Postdoctoral Research Associate- 2020-2022
TCR independent Treg expansion to ameliorates autoimmune diseases Type 1 diabetes mellitus, Systemic lupus erythematosus
Immunophenotyping to study dose dependent effect of OX40-Jagged1 on thymic Treg expansion
Characterize the clones to express OX40 receptor in human peripheral blood to expand Treg to achieve therapeutic relevance
Studied TFH dependent b-cell mediated immune responses in the pathogenesis of lupus nephritis (LN)
Explore the role of OX40 L -Jagged 1 in amelioration of LN
Junior Research Fellow- Department of Science & Technology 2011-2013
Senior Research Fellow- Department of Science & Technology 2013-2014
Worked in independent Department of Science & Technology sponsored project “Role of Class II histone deacetylases in the regulation of insulin gene transcription
2011-2014
Explored the role of class II HDACs 4,5,7,9 expression at different concentration of glucose
Studied the correlation of functional inactivation of class 2 HDACs in insulin gene expression
“Effect of Acute inflammation on histone H3 modifications in Rat testis and its implications in Testicular Steroidogenesis”
Characterized the molecular mechanisms of the inhibitory role of TNF-α on testicular steroidogenesis and gonadal functions
TNF-α suppressed histone H3 acetylation as well as methylation, and concomitantly, increased the histone deacetylases activity in Leydig cells
DAX1 as the key mediator of the TNF-α effect and demonstrated that knockdown of DAX1 restored normal steroidogenesis
Summary of Ph.D
Thesis Study on glucose-dependent expression of PAX6 and HDAC7 in the regulation of pancreatic β- cell function
The paired homeodomain-containing transcription factor, paired box6 (PAX6), has shown to play pivotal roles in beta-cell function, including insulin biosynthesis and secretion
However, glucose regulation of PAX6 and its role in pancreatic beta-cell function is not well understood
Studies on the pathways of intracellular signal transduction that regulate Pax6 expression demonstrated that glucose mediated activation of PKC and JNK/p38 MAPK pathway down-regulates Pax6 expression in pancreatic beta-cells
Suppression of Pax6 in high glucose, in turn, decreases the expression of PTEN while increasing cyclins A1/D1
This may be one of the possible mechanisms subserving the high glucose-induced cell viability in beta-cells
High glucose significantly increased histone H3 acetylation and concurrently decreased total HDAC activity
Further, it was found that HDAC7 was significantly down-regulated in high glucose treated pancreatic beta-cells
Experiments from siRNA mediated knockdown suggest that PAX6 regulates HDAC7 expression in response to glucose concentrations
Furthermore, glucose by itself modulates the subcellular localization of HDAC7 through PKD1 mediated phosphorylation
The chemical inhibition of HDAC7 significantly increased insulin mRNA levels at low glucose concentrations, suggesting its vital role in regulation of insulin gene transcription
M Phil, Research work
Clinical correlation among Non-alcoholic fatty liver disease, Type-2 Diabetes mellitus, Hepatocellular carcinoma
1)Haematological parameters such as WBC count, platelet count and Hb% were studied
2) Fasting blood glucose, post prandial blood glucose serum protein, Albumin: Globulin ratio and bilirubin were determined
3) Activities of liver marker enzymes such as serum transaminases (SGOT
and SGPT) and alkaline phosphatase were studied
4) Alterations in the lipid profile including total cholesterol, triglycerides and
Biomedical Laboratory Scientist at Rigshospitalet, Clinical Biochemistry Research Dept.Biomedical Laboratory Scientist at Rigshospitalet, Clinical Biochemistry Research Dept.
Manager - Operations and Human Resources at Athma Hospitals And Research Private LimitedManager - Operations and Human Resources at Athma Hospitals And Research Private Limited