Asthmatic lungs typically respond to inhaled allergens with exaggerated reductions in airway function. This phenomenon is termed airway hyper-responsiveness (AHR) and can be life threatening. AHR is not a simple reaction but is the culmination of multiple processes that manifest over a huge range of length and time scales. At one extreme, molecular signaling and interactions determine the force generated by airway smooth muscle cells (ASMCs). At the other extreme, contraction of the ASMCs is converted into a dynamic and complex constriction of branched airways that patients perceive by increased difficulty in breathing. Furthermore, asthma therapies are predominately pharmacological and operate at the molecular level, yet clinical outcomes are measured at the level of the whole lung. These two extremes are linked by numerous events operating at intermediate ranges of scale. These complex characteristics of AHR limit our understanding and ability to control asthma and will continue to confound research studies that only address responses at a single scale. Complex multi-scale systems cannot, by their very nature, be understood by studies limited to a few parameters. Consequently, this proposal will follow the innovative and alternative systems approach of developing a multi-scale experimental and computational model of AHR. We will initially determine how Ca2+ oscillations and the kinetics of cross-bridge cycling between actin and myosin molecules determine force production by ASMCs. Subsequently, we will determine how this force production distorts the airway wall and brings about airway narrowing throughout the lung. This will be achieved by the collaboration of a multidisciplinary group of investigators with experimental and mathematical expertise who will integrate our current knowledge and understanding of AHR at different cellular and tissue levels into a mathematical and computational model of AHR. The model will initially include phenomena that meet the criteria of being essential for airway contraction, of clear importance to AHR and experimentally accessible for iterative validation. In future studies, this model will be refined by the addition of relevant details. The model will be used to make specific predictions of molecular, cellular and tissue behavior and suggest critical experiments. In combination with extensive iteration between theory and experimentation, the sub-sections of the model will be refined and validated to identify the fundamental parameters that link the successive processes or scales. The results of this investigation will lead to an improved understanding of the link between the basic cellular pathophysiology and the whole lung response in asthma and other obstructive lung diseases This will improve the diagnosis of cause and effectiveness of treatment of these diseases. In addition, because AHR is clearly a complicated symptom, this investigation will evaluate the effectiveness of addressing disease with a systems biology approach. Many individuals in the USA suffer from asthma, a condition that is characterized by an exaggerated airway contraction or airway hyper-responsiveness (AHR). This response is extremely complicated being initiated at the molecular level by airborne allergens or stimuli and culminating at the organ level with difficulty in breathing. The objective of this research is to develop an understanding of this sequence of events by using a mathematical framework to guide and integrate experimental studies that elucidate the details of each process involved. With this approach, the key events in AHR can be identified and targeted for therapeutic intervention. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Exploratory/Developmental Grants Phase II (R33)
Project #
1R33HL087788-01A1
Application #
7292139
Study Section
Special Emphasis Panel (ZHL1-CSR-K (M1))
Program Officer
Banks-Schlegel, Susan P
Project Start
2007-08-01
Project End
2010-05-31
Budget Start
2007-08-01
Budget End
2008-05-31
Support Year
1
Fiscal Year
2007
Total Cost
$199,113
Indirect Cost
Name
University of Vermont & St Agric College
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
066811191
City
Burlington
State
VT
Country
United States
Zip Code
05405
Ma, Baoshun; Smith, Bradford J; Bates, Jason H T (2015) Resistance to alveolar shape change limits range of force propagation in lung parenchyma. Respir Physiol Neurobiol 211:22-8
Bates, Jason H T; Stevenson, Chelsea A; Aliyeva, Minara et al. (2012) Airway responsiveness depends on the diffusion rate of methacholine across the airway wall. J Appl Physiol 112:1670-7
Suki, Bela; Bates, Jason H T; Frey, Urs (2011) Complexity and emergent phenomena. Compr Physiol 1:995-1029
Suki, Bela; Bates, Jason H T (2011) Lung tissue mechanics as an emergent phenomenon. J Appl Physiol 110:1111-8
Schwartz, Benjamin L; Anafi, Ron C; Aliyeva, Minara et al. (2011) Effects of central airway shunting on the mechanical impedance of the mouse lung. Ann Biomed Eng 39:497-507
Bates, Jason H T; Irvin, Charles G; Farré, Ramon et al. (2011) Oscillation mechanics of the respiratory system. Compr Physiol 1:1233-72
Tawhai, Merryn H; Bates, Jason H T (2011) Multi-scale lung modeling. J Appl Physiol 110:1466-72
Bullimore, Sharon R; Siddiqui, Sana; Donovan, Graham M et al. (2011) Could an increase in airway smooth muscle shortening velocity cause airway hyperresponsiveness? Am J Physiol Lung Cell Mol Physiol 300:L121-31
Politi, Antonio Z; Donovan, Graham M; Tawhai, Merryn H et al. (2010) A multiscale, spatially distributed model of asthmatic airway hyper-responsiveness. J Theor Biol 266:614-24
Khan, Mohammad Afzal; Ellis, Russ; Inman, Mark D et al. (2010) Influence of airway wall stiffness and parenchymal tethering on the dynamics of bronchoconstriction. Am J Physiol Lung Cell Mol Physiol 299:L98-L108

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