Aaron Barchowsky, PhD

The primary focus of current research is investigating the cellular and molecular mechanisms underlying human diseases caused by environmental exposures to metals and chronic changes in cellular redox status. In vivo and cell cultured based studies focus on the molecular pathology and etiology of vascular disease and lost regenerative capacity caused by chronic exposure to low levels of arsenic in drinking water. The cell signaling pathways that mediate arsenic-stimulated pathogenic phenotypic changes in endothelial,muscle, and stem cells are being investigated.  Research is also focused on critical questions of how environmental arsenic exposures promote unhealthy aging, limit tissue maintenance, and impair tissue stem cell function.

1978  North Carolina State University, Raleigh, NC    BS Zoology

1984  Duke University, Durham, NC    PhD Pharmacology

I currently direct the Pitt Public Health core curriculum course in Environmental Health and Disease (EOH 2013).  I also lecture in a range of courses in Pitt Public Health and the School of Medicine in areas including environmental epidemiology, environmental exposures, risk assessment, molecular cell signaling pathways, pathophysiology, toxicology, angiogenesis, and medical pharmacology.  In addition, I direct the Department of Environmental and Occupational Health MS and PhD program in Environmental Health Sciences.

Cheiki A, C Wallace, C St Croix, C Cohen, WY Tang, P Wipf, PV Benos, F Ambrosio, A Barchowsky. Mitochondria are a substrate of cellular memory. Free Radic Biol Med. 130:528-541, 2019 PMID: 30472365

 

Cheikhi A, A Barchowsky, A Sahu, SN Shinde, A Pius, ZJ Clemens, H Li, CA Kennedy, JD Hoeck, M Franti, F Ambrosio. Klotho: An elephant in aging research. J Gerontol A Biol Sci Med Sci. 2019 doi: 10.1093/gerona/glz061 PMID: 30843026

 

Oberoi S, B Devleesschauwer, HJ Gibb, A Barchowsky. Global burden of cancer and coronary heart disease resulting from dietary exposure to arsenic, 2015. Environ Res 171:185-192, 2019. PMID: 30665120

 

Sahu A, H Mamiya, S Shinde, A Cheikhi, L Winter, N Vo, D Stolz, V Roginskayya, WY Tang, C St. Croix, M Franti, L Sanders, B Van Houten, T Rando, A Barchowsky and Ambrosio F. Age-related declines in a-Klotho drive progenitor cell mitochondrial dysfunction and impaired muscle regeneration. Nat Commun. 9:4859, 2018. PMID: 30451844

 

Stearns-Reider K; D’Amore A; Beezhold K; Rothrauff BB;
Cavalli L; Wagner W; Vorp DA; Tsamis A; Shinde, S; Zhang C; Barchowsky A; Rando TA; Tuan RS; Ambrosio F.  Aging of the skeletal muscle extracellular matrix drives a stem cell fibrogenic conversion. Aging Cell 16:518-528, 2017. PMID: 28371268

 

Beezhold K, LR Klei, A Barchowsky. Regulation of cyclin D1 by arsenic and microRNA inhibits adipogenesis. Tox Lett 265:147-155, 2017. PMID: 27932253

 

Zhang C*, R Ferrari*, K Beezhold, K Stearns-Reider, A D’Amore, M Haschak, DB Stolz, PD. Robbins, A Barchowsky, F Ambrosio. Arsenic promotes NF-kB-mediated fibroblast dysfunction and matrix remodeling to impair muscle stem cell function. Stem Cells 34:732-42, 2015. PMID: 26537186

 

Cronican AA, NF Fitz, A Carter, M Saleem, S Shiva, A Barchowsky, R Koldamova, J Schug, and I Lefterov. Genome-wide alteration of histone H3K9 acetylation pattern in mouse offspring prenatally exposed to arsenic. PLOS ONE 8(2):e53478, 2013 PMID: 23405071.

 

Straub AC, KA Clark, MA Ross, AG Chandra, S Li, X Gao, PJ Pagano, DB Stolz, and A Barchowsky.  Arsenic-stimulated liver sinusoidal capillarization in mice requires NADPH oxidase-generated superoxide.  J. Clin. Invest. 118:3980-9, 2008. PMID:19033667