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Home > Physicians > Piantadosi, Claude A.
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Physicians

Claude A. Piantadosi, MD

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Claude A. Piantadosi, MD
Departments / Divisions
  • Medicine / Medicine-Pulmonary
  • Pathology
  • Anesthesiology

Address
DUMC 3315
Durham, NC 27710

Appointment Telephone
919-668-7630

Office Telephone
919-684-6143

Fax Telephone
919-684-6002

Training
  • MD, Johns Hopkins University School of Medicine (Maryland), 1975

Residency
  • Medicine, Johns Hopkins Hospital (Maryland), 1975-1977
  • Pulmonary and Critical Care Medicine, Duke University Medical Center, 1980-1981

Clinical Interests
Critical care medicine, interstitial lung diseases, sarcoidosis, pulmonary alveolar proteinosis, diving/hyperbaric medicine

Research Interests
Dr. Piantadosi's laboratory has special expertise in the pathogenic mechanisms of acute organ failure, particularly acute lung injury (ALI), with an emphasis on the molecular regulatory roles of the physiological gases— oxygen, carbon monoxide, and nitric oxide— as they relate to the damage responses to acute inflammation. The basic science focuses on oxidative processes and redox-regulation, especially the molecular mechanisms by which reactive oxygen and nitrogen species transmit biological signals involved in the maintenance of energy metabolism and mitochondrial health, but also contribute to pathogenesis and to the resolution of tissue injury.

Clinically, ALI and the related syndrome of multiple organ failure has a high mortality, which is related to the host inflammatory response, but is not well understood scientifically; thus, the laboratory is devoted to understanding these mechanisms in the context of the host response to relevant but well-controlled experimental manipulations including hyperoxia, bacterial infections, toxic drugs, and cytokine/chemokine signals. The approach relies on animal models, mainly transgenic and knockout mice, and cell models, especially lung and heart cells to evaluate and understand the physiology, pathology, and cell and molecular biology of the injury responses, to test independent and integrated mechanisms, and to devise interventions to prevent damage.

Apart from the lung, significant work is devoted to understanding damage to the heart, brain, liver, and kidney caused by these immune mechanisms, specifically emphasizing the role of mitochondria, key targets and sources of oxidative damage. This damage compromises their ability to support energy homeostasis and advanced cellular functions, and impacts on the important roles these organelles play in cell death by apoptosis and necrosis as well as in the resolution of cellular damage and inflammation.

Industry Relationships and Collaborations (What's this?)

This faculty member has no reported relationships with industry.

Representative Publications
Piantadosi, CA. Regulation of mitochondrial processes by protein S-nitrosylation. Biochimica et Biophysica Acta: international journal of biochemistry and biophysics. 2012;1820:712-721. (2012) Abstract

Bartz, RR; Suliman, HB; Fu, P; Welty-Wolf, K; Carraway, MS; MacGarvey, NC; Withers, CM; Sweeney, TE; Piantadosi, CA. Staphylococcus aureus sepsis and mitochondrial accrual of the 8-oxoguanine DNA glycosylase DNA repair enzyme in mice. American Journal of Respiratory and Critical Care Medicine. 2011;183:226-233. (2011) Abstract

Piantadosi, CA; Withers, CM; Bartz, RR; MacGarvey, NC; Fu, P; Sweeney, TE; Welty-Wolf, KE; Suliman, HB. Heme oxygenase-1 couples activation of mitochondrial biogenesis to anti-inflammatory cytokine expression. Journal of Biological Chemistry. 2011;286:16374-16385. (2011) Abstract

Sheng, H; Reynolds, JD; Auten, RL; Demchenko, IT; Piantadosi, CA; Stamler, JS; Warner, DS. Pharmacologically augmented S-nitrosylated hemoglobin improves recovery from murine subarachnoid hemorrhage. Stroke. 2011;42:471-476. (2011) Abstract

Sweeney, TE; Suliman, HB; Hollingsworth, JW; Welty-Wolf, KE; Piantadosi, CA. A toll-like receptor 2 pathway regulates the Ppargc1a/b metabolic co-activators in mice with Staphylococcal aureus sepsis. PLoS One. 2011;6:e25249. (2011) Abstract

Carraway, MS; Suliman, HB; Jones, WS; Chen, CW; Babiker, A; Piantadosi, CA. Erythropoietin activates mitochondrial biogenesis and couples red cell mass to mitochondrial mass in the heart. Circulation Research. 2010;106:1722-1730. (2010) Abstract

Carre, JE; Orban, JC; Re, L; Felsmann, K; Iffert, W; Bauer, M; Suliman, HB; Piantadosi, CA; Mayhew, TM; Breen, P; Stotz, M; Singer, M. Survival in critical illness is associated with early activation of mitochondrial biogenesis. American Journal of Respiratory and Critical Care Medicine. 2010;182:745-751. (2010) Abstract

Suliman, HB; Sweeney, TE; Withers, CM; Piantadosi, CA. Co-regulation of nuclear respiratory factor-1 by NFkappaB and CREB links LPS-induced inflammation to mitochondrial biogenesis. Journal of Cell Science. 2010;123:2565-2575. (2010) Abstract

Allen, BW; Stamler, JS; Piantadosi, CA. Hemoglobin, nitric oxide and molecular mechanisms of hypoxic vasodilation. Trends in Molecular Medicine. 2009;15:452-460. (2009) Abstract

Reynolds, CM; Suliman, HB; Hollingsworth, JW; Welty-Wolf, KE; Carraway, MS; Piantadosi, CA. Nitric oxide synthase-2 induction optimizes cardiac mitochondrial biogenesis after endotoxemia. Free Radical Biology and Medicine. 2009;46:564-572. (2009) Abstract

Gutsaeva, DR; Carraway, MS; Suliman, HB; Demchenko, IT; Shitara, H; Yonekawa, H; Piantadosi, CA. Transient hypoxia stimulates mitochondrial biogenesis in brain subcortex by a neuronal nitric oxide synthase-dependent mechanism. The Journal of Neuroscience. 2008;28:2015-2024. (2008) Abstract

Piantadosi, CA. Carbon monoxide, reactive oxygen signaling, and oxidative stress. Free Radical Biology and Medicine. 2008;45:562-569. (2008) Abstract

Piantadosi, CA; Carraway, MS; Babiker, A; Suliman, HB. Heme oxygenase-1 regulates cardiac mitochondrial biogenesis via Nrf2-mediated transcriptional control of nuclear respiratory factor-1. Circulation Research. 2008;103:1232-1240. (2008) Abstract

Demchenko, IT; Welty-Wolf, KE; Allen, BW; Piantadosi, CA. Similar but not the same: normobaric and hyperbaric pulmonary oxygen toxicity, the role of nitric oxide. American Journal of Physiology: Lung Cellular and Molecular Physiology. 2007;293:L229-L238. (2007) Abstract

Haden, DW; Suliman, HB; Carraway, MS; Welty-Wolf, KE; Ali, AS; Shitara, H; Yonekawa, H; Piantadosi, CA. Mitochondrial biogenesis restores oxidative metabolism during Staphylococcus aureus sepsis. American Journal of Respiratory and Critical Care Medicine. 2007;176:768-777. (2007) Abstract

Piantadosi, CA. Early development of near-infrared spectroscopy at Duke University. Journal of Biomedical Optics. 2007;12:062102. (2007) Abstract

Suliman, HB; Carraway, MS; Ali, AS; Reynolds, CM; Welty-Wolf, KE; Piantadosi, CA. The CO/HO system reverses inhibition of mitochondrial biogenesis and prevents murine doxorubicin cardiomyopathy. Journal of Clinical Investigation. 2007;117:3730-3741. (2007) Abstract

Suliman, HB; Carraway, MS; Tatro, LG; Piantadosi, CA. A new activating role for CO in cardiac mitochondrial biogenesis. Journal of Cell Science. 2007;120:299-308. (2007) Abstract

Piantadosi, CA; Suliman, HB. Mitochondrial transcription factor A induction by redox activation of nuclear respiratory factor 1. Journal of Biological Chemistry. 2006;281:324-333. (2006) Abstract

Welty-Wolf, KE; Carraway, MS; Ortel, TL; Ghio, AJ; Idell, S; Egan, J; Zhu, X; Jiao, JA; Wong, HC; Piantadosi, CA. Blockade of tissue factor-factor X binding attenuates sepsis-induced respiratory and renal failure. American Journal of Physiology: Lung Cellular and Molecular Physiology. 2006;290:L21-L31. (2006) Abstract

Suliman, HB; Welty-Wolf, KE; Carraway, MS; Schwartz, DA; Hollingsworth, JW; Piantadosi, CA. Toll-like receptor 4 mediates mitochondrial DNA damage and biogenic responses after heat-inactivated E. coli. The FASEB Journal. 2005;19:1531-1533. (2005) Abstract

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Updated: Dec. 12, 2006
Published: Dec. 12, 2006
URL: http://www.dukehealth.org/physicians/claude_a_piantadosi