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Peter Mancuso

Peter Mancuso, Ph.D.

Associate Professor, Environmental Health Sciences

6627 SPH Tower
1415 Washington Heights
Ann Arbor, Michigan 48109-2029

Office: (734) 615-5158; Fax: (734) 763-8095

E-mail: pmancuso@umich.edu

Website(s): Research Laboratory: Pulmonary Immunology and Adipokine Biology

Curriculum Vitae (PDF, 179,534 KB)

Professional Summary

Peter Mancuso is an interdisciplinary scientist whose research focuses on adipocyte derived hormones, eicosanoids, and environmental exposures that regulate pulmonary innate immune responses. He has used cellular, molecular and integrative biology to assess the effects of the eicosanoids (prostaglandins and leukotrienes), obesity, malnutrition, and tobacco smoke exposure on alveolar macrophage biology and pulmonary responses to bacterial infection. He also participates in the Graduate Program in Immunology. He is a member of the American Association of Immunologists and the American Thoracic Society. Previous to his academic appointments, he was employed as a food scientist in research and development in the food industry.

Courses Taught

EHS625: Environment and the Immune Response
EHS639: Pathophysiology of Obesity

Education

Ph.D., Physiology, University of Tennessee, 1996
M.S., Food Science and Nutrition, University of Tennessee, 1987
B.S., Food Science, Purdue University, 1985
Post-Doctoral Fellowship, University of Michigan Medical Center, Lung Cell and Molecular Biology, 1997-1999

Research Interest & Projects

Malnutrition is arguably the most common cause of immune suppression, from a global perspective, and a significant risk factor for infectious disease. The mechanisms responsible for impaired innate immune responses against bacterial infections arising from energy malnutrition are poorly understood. Leptin is a hormone produced by adipose tissue that is reduced in the energy malnourished and is known to regulate innate immune responses. We have observed that mice rendered leptin-deficient by genetic means or by fasting are more susceptible to bacterial pneumonia. We are currently exploring the intracellular signaling pathways by which leptin regulates alveolar macrophage function, proinflammatory mediator synthesis, and pulmonary host defense against bacterial pathogens.

In addition to malnutrition, tobacco smoke is also a potent immune suppressant and smokers are very susceptible to bacterial pneumonia. Previous studies have demonstrated that pulmonary bacterial clearance and alveolar macrophage antibacterial functions are reduced in smokers. However, the mechanisms responsible for these defects are poorly understood. We are currently exploring the role of nicotine in cigarette smoke induced suppression of pulmonary innate immune responses against bacterial pathogens.

Regulation of Pulmonary Host Defense by Leptin
Principal Investigator: Mancuso, P.
Sponsor: NIH

Use of LTB4 as a Therapeutic Agent for the Treatment of Pneumococcal Pneumonia
Principal Investigator: Mancuso, P.
Sponsor: Adventis Pharma

Obesity, Adipokines and Cardiovascular Risk Factors in Women
Principal Investigator: Wildman, R.
Sponsor: NIH

Obesity Subtypes, Adiponectin and Incident Stroke among Postmenopausal Women
Principal Investigator: Wildman, R.
Sponsor: NIH

Selected Publications

Mancuso, P., Rahman, A., Hershey, S.D., Dandu, L., Nibbelink, K.A. and Simpson, R.U. (2008). 1,25-dihydroxyvitamin-D3 treatment reduces cardiac hypertrophy and left ventricular diameter in spontaneously hypertensive heart failure prone (cp/+) rats independent of changes in serum leptin. Journal of Cardiovascular Pharmacology, 51, 559-64.

Sowers, M.F., Wildman, R., Mancuso, P., Carrie, A.A., Karvonen-Guiterrez, Rillamas-Sun, E., McConnell, D., Li, X. and Nan B. (2008). Change in adipocytokines and ghrelin with menopause and body size. Maturistas, 2, 149-157 .

Wildman, R.P., Mancuso, P., Wang, C., Kim, M., Scherer, P.E. and Sowers, M.F. (2008). Cardiovascular risk factors in relation to adipocytokine and ghrelin levels in menopausal women: Cross-sectional and longitudinal associations. International Journal of Obesity, 740-748.

Hsu, A., Phipps, J., Aronoff, D.M., Carstens, J.K. and Mancuso, P. (2007). Leptin improves pulmonary bacterial clearance and survival in ob/ob mice during pneumococcal pneumonia. Clinical and Experimental Immunology, November, 332-339.

Flamand, N., Mancuso, P., Serezani, C.H.C. and Brock,T.G. (2007). Leukotrienes: Mediators that have been typecast as villains Cellular and Molecular Life Sciences, 64, 2657-2670.

Lugo, J.Z., Price, S, Miller, J.E., Ben-David, I., Mancuso, P., Weinberg, J.B. and Younger, J.G. (2007). Lipopolysaccharide O-antigen and promotes persist murine bacteremia. Shock, 27, 186-191.

Mancuso, P., Huffmangle, G., Olszewski, M., Phipps, J. and Peters-Golden, M. (2006). Leptin corrects host defense defects following acute starvation in murine pneumococcal pneumonia. Am J Respir Crit Care Med, 173(2), 212-218.

Serezani, C.H., Aronoff, D.M., Jancar, S., Mancuso, P. and Peters-Golden, M. (2005). Leukotrienes enhance the bactericidal activity of alveolar macrophages against Klebsiella pneumoniae through the activation of NADPH oxidase. Blood, 106, 1067-1075.