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* (Pharmacy Faculty Profile)

Diane Allen-Gipson, M.S., Ph.D. A-9044-2012

Diane Allen-Gipson, M.S., Ph.D.

Adjunct Associate Professor, Dept of Internal Medicine, Division of Pulmonary, Critical Care, Sleep and Allergy Medicine

Affiliate Faculty Member, Health Outcome and Behavior

Affiliate Faculty Member, Cancer Biology and Evolution

Contact Info

  • 12901 Bruce B. Downs Blvd., MDC 30
    Tampa FL 33612
  • Academic Email: dallengi@usf.edu
  • Academic Phone: (813) 974-7225
  • View My C.V.

Education

  • PhD, Pharmacy, Florida A&M University, 2000
  • MS, Pharmacology/Toxicology, Florida A & M University, 1997
  • BS, Biological Sciences, University of Central Florida, 1990
  • AA, Biological Sciences, University of South Florida, 1987

Interdisciplinary and Emerging Signature Programs

  • Allergy, Immunology & Infectious Disease
  • Asthma Center of Excellence
  • Biomedical Engineering & Nanomedicine
  • Cancer Biology
  • Cardiovascular
  • Cardiovascular Sciences
  • Cellular and Molecular Biology
  • Environmental & amp; Global Health
  • Other
  • Pulmonary Physiology
  • Women & Children's Health

Research Interests

  • Research Focus:
  • Exposure to cigarette smoke is responsible for a considerable amount of pulmonary diseases including chronic bronchitis, emphysema, carcinoma of the lung, and chronic obstructive pulmonary disease (COPD) and excessive alcohol consumption also contributes to the comorbidities associated with these diseases. COPD is the only chronic disease growing in mortality in the USA and afflicts over 23 million people where at least 12 million remains undiagnosed. Furthermore, veterans are much more likely than non-veterans to have ever smoked (74% compared to 48%). By estimation of the US Department of Veteran Affairs, chronic inflammatory disorder, including asthma and COPD, is a common problem among veterans, accounting for ∼ 16% of VA hospital admissions and a third of admissions to all VA medical services, driving the need to develop novel research strategies to address the pathogenesis of these disorders. Our lab focuses on mechanisms controlling repair of bronchial epithelium particularly, adenosine signal pathway and its role of epithelial injury in airway diseases associated with cigarette smoke and/or in combination with alcohol exposure. Adenosine, an endogenous nucleoside has been recognized as an important modulator of hypoxic, ischemic and inflammatory process critical to both tissue homeostasis and tissue injury. However, the mechanisms by which adenosine-mediated airway wound healing and repair occurs after exposure to injurious agents like cigarette smoke has not been investigated. In addition to understanding the mechanisms involved in adenosine-mediated wound repair our lab has a growing interest in targeting efforts to reduce existing disparities in mortality rates particularly associated with smoke-related lung diseases and lung cancer. We recognized mortality from all causes is higher for persons with fewer years of education and for minorities including but not limited to Black and Hispanic population still remains unknown, which diseases contribute most to these disparities.
  • Laboratory Activities:
  • We are interested in understanding the dynamics of the receptor-mediated action of adenosine as well as investigating adenosines mechanistic signaling pathways associated with ciliary motility and clearance, pro-and- anti-inflammatory cytokine production, cell adhesion and remodeling and wound repair under conditions of cigarette smoke and/or alcohol exposure, and oxidative stress. In addition, our lab will focus on developing new therapeutic drug target and delivery systems as it relates to airway injury and repair via adenosine signaling pathway. We believe the distribution and varied effects of adenosine receptors in the epithelial airway could have for the most part, important implication in understanding chronic inflammatory diseases such as asthma and chronic obstructive pulmonary disease (COPD) and smoke-related lung cancer.
  • Methodology incorporated in our lab includes but not limited to:
  • • Receptor-Ligand binding Studies
  • • 3H Thymidine Incorporation Studies
  • • HPLC
  • • Molecular Biology Techniques i.e., Western Blots, immunoprecipations assays
  • • Genetic manipulations (Transfections)
  • • Ciliary Motility Studies (SAVA)
  • • Kinase Studies (PKA, PKC and PKG)
  • • Small animal studies (In vivo and Ex vivo)

Recent Publications

  • Fukumoto J, Fukumoto I, Parthasarathy PT, Cox R, Huynh B, Ramanathan GK, Venugopal RB, Allen-Gipson DS, Lockey RF, Kolliputi N. NLRP3 Deletion Protects from Hyperoxia-Induced Acute Lung Injury. American journal of physiology. Cell physiology. , 2013.
  • Allen-Gipson DS, Zimmerman MC, Zhang H, Castellanos G, O''Malley JK, Alvarez-Ramirez H, Kharbanda K, Sisson JH, Wyatt TA. Smoke extract impairs adenosine wound healing. American journal of respiratory cell and molecular biology. 48(5) : 665-73, 2013.
  • Simet SM, Wyatt TA, DeVasure J, Yanov D, Allen-Gipson D, Sisson JH. Alcohol increases the permeability of airway epithelial tight junctions in Beas-2B and NHBE cells. Alcoholism, clinical and experimental research. 36(3) : 432-42, 2012.
  • Allen-Gipson DS, Blackburn MR, Schneider DJ, Zhang H, Bluitt DL, Jarrell JC, Yanov D, Sisson JH, Wyatt TA. Adenosine activation of A(2B) receptor(s) is essential for stimulated epithelial ciliary motility and clearance. American journal of physiology. Lung cellular and molecular physiology. 301(2) : L171-80, 2011.
  • Allen-Gipson DS, Jarrell JC, Bailey KL, Robinson JE, Kharbanda KK, Sisson JH, Wyatt TA. Ethanol blocks adenosine uptake via inhibiting the nucleoside transport system in bronchial epithelial cells. Alcoholism, clinical and experimental research. 33(5) : 791-8, 2009.
  • Poole JA, Alexis NE, Parks C, MacInnes AK, Gentry-Nielsen MJ, Fey PD, Larsson L, Allen-Gipson D, Von Essen SG, Romberger DJ. Repetitive organic dust exposure in vitro impairs macrophage differentiation and function. The Journal of allergy and clinical immunology. 122(2) : 375-82, 382.e1-4, 2008.
  • Slager RE, Allen-Gipson DS, Sammut A, Heires A, DeVasure J, Von Essen S, Romberger DJ, Wyatt TA. Hog barn dust slows airway epithelial cell migration in vitro through a PKCalpha-dependent mechanism. American journal of physiology. Lung cellular and molecular physiology. 293(6) : L1469-74, 2007.
  • Allen-Gipson DS, Spurzem K, Kolm N, Spurzem JR, Wyatt TA. Adenosine promotion of cellular migration in bronchial epithelial cells is mediated by the activation of cyclic adenosine monophosphate-dependent protein kinase A. Journal of investigative medicine : the official publication of the American Federation for Clinical Research. 55(7) : 378-85, 2007.
  • Allen-Gipson DS, Wong J, Spurzem JR, Sisson JH, Wyatt TA. Adenosine A2A receptors promote adenosine-stimulated wound healing in bronchial epithelial cells. American journal of physiology. Lung cellular and molecular physiology. 290(5) : L849-55, 2006.
  • Allen-Gipson DS, Floreani AA, Heires AJ, Sanderson SD, MacDonald RG, Wyatt TA. Cigarette smoke extract increases C5a receptor expression in human bronchial epithelial cells. The Journal of pharmacology and experimental therapeutics. 314(1) : 476-82, 2005.
  • Allen-Gipson DS, Romberger DJ, Forget MA, May KL, Sisson JH, Wyatt TA. IL-8 inhibits isoproterenol-stimulated ciliary beat frequency in bovine bronchial epithelial cells. Journal of aerosol medicine : the official journal of the International Society for Aerosols in Medicine. 17(2) : 107-15, 2004.
  • Floreani AA, Wyatt TA, Stoner J, Sanderson SD, Thompson EG, Allen-Gipson D, Heires AJ. Smoke and C5a induce airway epithelial intercellular adhesion molecule-1 and cell adhesion. American journal of respiratory cell and molecular biology. 29(4) : 472-82, 2003.
  • Heiman AS, Allen-Gipson D. Cytokines potentiate human eosinophil superoxide generation in the presence of N(omega)-nitro-L-arginine methyl ester. International journal of immunopharmacology. 22(2) : 171-81, 2000.
  • Allen-Gipson DS, Chen M, Heiman AS. Regulation of 10P2 murine mast cell proliferation and secretory function by stem cell factor or IL-9. Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.). 217(4) : 439-44, 1998.