Final Program
h6okmgq
h6okmgq
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
WEDNESDAY • MAY 18 339<br />
• learn new findings about the identification and validation of new asthma drug<br />
targets;<br />
• screen drug candidates that improve lung function;<br />
• gain knowledge on GPCR signaling in the lung.<br />
There is still an urgent need to develop new and improved therapy for asthma.<br />
G-protein coupled receptors (GPCRs) are the targets of more than 50% of all known<br />
pharmaceuticals. Current mainstay asthma therapies including beta-agonists,<br />
anticholinergics, and leukotriene inhibitors, all directly target GPCRs. Recent studies<br />
have identified several GPCRs and many of them unexpectedly as new potential<br />
targets for asthma therapy. In this session, we will bring a high-caliber list of experts<br />
to discuss the latest developments in this exciting area that promises to change the<br />
face of asthma medicine in the coming decades.<br />
Chairing: Q. Lu, PhD, Boston, MA<br />
R. Penn, PhD, Philadelphia, PA<br />
9:00 Targeting Calcium Sensing Receptor (CaSR) in Allergic<br />
Asthma<br />
D. Riccardi, PhD, Cardiff, United Kingdom<br />
9:20 Function and Targeting of Proton-Sensing GPCR OGR1 in ASM<br />
R. Penn, PhD, Philadelphia, PA<br />
9:40 Bitter Taste Receptors as Targets for Novel Bronchodilators<br />
D.A. Deshpande, PhD, Philadelphia, PA<br />
10:00 Screening GPCR Targets with Force<br />
R. Krishnan, PhD, Boston, MA<br />
10:20 Structural Insights into ß2-Adrenergic Receptor Signaling<br />
R. Sunahara, PhD, La Jolla, CA<br />
10:40 Cholecystokinin (CCK) and Its Receptor CCKAR as Novel<br />
Therapeutic Targets for Asthma<br />
Q. Lu, PhD, Boston, MA<br />
This session and the International Conference are supported by an educational grant from<br />
AstraZeneca LP.<br />
All CME sessions have been planned and implemented in accordance with the Essential<br />
Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME)<br />
and are free of the control of commercial interests.<br />
D8<br />
BASIC • CLINICAL • TRANSLATIONAL<br />
SCIENTIFIC SYMPOSIUM<br />
CME Credits Available: 2.0<br />
ATS MYTHBUSTERS: ABERRANT TISSUE<br />
REGENERATION IS A PRIMARY DRIVER OF COPD<br />
PATHOGENESIS<br />
Assemblies on Respiratory Cell and Molecular Biology; Allergy, Immunology<br />
and Inflammation; Clinical Problems; Critical Care; Environmental,<br />
Occupational and Population Health; Microbiology, Tuberculosis and<br />
Pulmonary Infections; Pulmonary Circulation; Pulmonary Rehabilitation;<br />
Respiratory Structure and Function; Thoracic Oncology<br />
9:00 a.m. - 11:00 a.m. MOSCONE CENTER<br />
Room 2016/2018 (West Building, Level 2)<br />
Target Audience<br />
Lung health care providers, scientists and investigators interested or involved in<br />
basic, translational and clinical research related to lung biology and clinical<br />
aspects of COPD and related human lung diseases. Research and care<br />
providers engaged in pulmonary and critical care medicine.<br />
Objectives<br />
At the conclusion of this session, the participant will be able to:<br />
• understand how aberrant airway and alveolar regeneration contributes to the<br />
pathogenesis of airway remodeling, emphysema and inflammation in COPD;<br />
• learn how aberrant tissue repair mechanisms interact with other components<br />
of COPD pathogenesis (oxidative stress, inflammation, altered innate<br />
immunity and host-microbe interactions);<br />
• understand how to translate the novel knowledge about the role of aberrant<br />
tissue regeneration in COPD pathogenesis into clinically relevant<br />
“personalized” (precision medicine) approaches to better prevent, diagnose<br />
and treat COPD.<br />
This session continues the “ATS Mythbusters” series focused on emerging areas<br />
of translational lung biology and medicine. The central theme of the current ATS<br />
Mythbuster session is recently evolved concept of abnormal airway and alveolar<br />
structural maintenance and regeneration as the driving force of COPD<br />
pathogenesis and progression. Recently developed data supporting this novel<br />
concept (“myth”) will be presented by the investigators who contributed to these<br />
discoveries and then discussed by internationally recognized leading scientists<br />
(“busters”) in the COPD field.<br />
Chairing: R. Shaykhiev, MD, PhD, New York, NY<br />
I. Petrache, MD, Denver, CO<br />
J.C. Hogg, MD, PhD, Vancouver, Canada<br />
9:00 Introduction to the Myth: Emerging Non-inflammatory Origins<br />
of COPD<br />
I. Petrache, MD, Denver, CO<br />
9:15 Altered Epithelial Barrier Function in COPD Airways<br />
I.H. Heijink, PhD, Groningen, Netherlands<br />
9:30 Pathologic <strong>Program</strong>ming of Airway Basal Stem Cells in COPD<br />
R. Shaykhiev, MD, PhD, New York, NY<br />
9:45 Epithelial-Mesenchymal Interactions and Airway Fibrosis in<br />
COPD<br />
S. Nishimura, MD, San Francisco, CA<br />
10:00 Wnt Signaling Shift in COPD and Aging<br />
M. Konigshoff, MD, PhD, Munich, Germany<br />
10:15 Telomere Dysfunction and Alveolar Stem Cell Failure in<br />
Emphysema<br />
M. Armanios, MD, Baltimore, MD<br />
10:30 “Mythbusters” Discussion<br />
L.M. Fabbri, MD, Modena, Italy<br />
M. Saetta, MD, Padova, Italy<br />
S.I. Rennard, MD, Melbourn, United Kingdom<br />
P.J. Barnes, MD, DSc, London, United Kingdom<br />
WEDNESDAY MORNING<br />
ATS 2016 • San Francisco