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American Journal of Physiology-lung Cellular and Molecular Physiology | 1998

Repeated allergen inhalations induce DNA synthesis in airway smooth muscle and epithelial cells in vivo

Reynold A. Panettieri; Richard Murray; Andrew J. Eszterhas; Gulsevil Bilgen; James G. Martin

Airway smooth muscle (ASM) mass appears to be increased in the bronchi of patients with chronic severe asthma. Although the precise mechanisms that induce these changes are unknown, increases in ASM mass are caused, in part, by ASM cell proliferation. After allergen challenge in rats, it has been possible to demonstrate an increase in ASM mass by morphometric techniques. To examine whether hyperplasia is involved in ASM cell growth in vivo, we investigated whether repeated allergen challenges in sensitized Brown Norway rats stimulated DNA synthesis in airway epithelial and ASM cells. Animals that were actively sensitized to ovalbumin (OA) received either three aerosolized OA or saline challenges at 5-day intervals. DNA synthesis was measured by indirect immunohistochemical techniques with an anti-bromodeoxyuridine (BrdU) antibody. OA inhalations increased ASM mass as determined by morphometry and also induced DNA synthesis in both airway epithelial and ASM cells in the airways of sensitized animals compared with saline-challenged control animals. ASM mass was increased in large- and medium-sized airways but not in small airways. However, the number of BrdU-positive ASM cells normalized to basement membrane length was also greater in the large- and medium-sized airways compared with that in the small airways. When the number of BrdU-positive epithelial cells was normalized to basement membrane length, there was no difference among airway sizes and the number of BrdU-positive epithelial cells. These data suggest that DNA synthesis is induced in both airway epithelial and ASM cells after inhalational antigen challenge.Airway smooth muscle (ASM) mass appears to be increased in the bronchi of patients with chronic severe asthma. Although the precise mechanisms that induce these changes are unknown, increases in ASM mass are caused, in part, by ASM cell proliferation. After allergen challenge in rats, it has been possible to demonstrate an increase in ASM mass by morphometric techniques. To examine whether hyperplasia is involved in ASM cell growth in vivo, we investigated whether repeated allergen challenges in sensitized Brown Norway rats stimulated DNA synthesis in airway epithelial and ASM cells. Animals that were actively sensitized to ovalbumin (OA) received either three aerosolized OA or saline challenges at 5-day intervals. DNA synthesis was measured by indirect immunohistochemical techniques with an anti-bromodeoxyuridine (BrdU) antibody. OA inhalations increased ASM mass as determined by morphometry and also induced DNA synthesis in both airway epithelial and ASM cells in the airways of sensitized animals compared with saline-challenged control animals. ASM mass was increased in large- and medium-sized airways but not in small airways. However, the number of BrdU-positive ASM cells normalized to basement membrane length was also greater in the large- and medium-sized airways compared with that in the small airways. When the number of BrdU-positive epithelial cells was normalized to basement membrane length, there was no difference among airway sizes and the number of BrdU-positive epithelial cells. These data suggest that DNA synthesis is induced in both airway epithelial and ASM cells after inhalational antigen challenge.


American Journal of Physiology-cell Physiology | 1989

A human airway smooth muscle cell line that retains physiological responsiveness

Reynold A. Panettieri; Richard Murray; L. R. DePalo; P. A. Yadvish; Michael I. Kotlikoff


American Journal of Respiratory Cell and Molecular Biology | 1995

alpha-Thrombin increases cytosolic calcium and induces human airway smooth muscle cell proliferation.

Reynold A. Panettieri; Ian P. Hall; C S Maki; Richard Murray


Chest | 1995

Repeated Allergen Inhalations Induce DNA Synthesis in Airway Smooth Muscle and Epithelial Cells In Vivo

Reynold A. Panettieri; Richard Murray; Gulsevil Bilgen; Andrew J. Eszterhas; James G. Martin


Chest | 2004

Auto-Adjusting Demand Oxygen Delivery System that Minimizes SaO2 Swings Between Rest and Exertion

Brian Tiep; Richard Murray; Mary Barnett; Rick Carter


Archive | 2016

airway smooth muscle and epithelial cells in vivo Repeated allergen inhalations induce DNA synthesis in

James G. Martin; Reynold A. Panettieri; Richard Murray; Andrew J. Eszterhas; Gulsevil Bilgen


Archive | 2015

Repeated Allergen Inhalations Induce DNASynthesis inAirway SmoothMuscleandEpithelial Cells InVivo

Reynold A. Panettieri; Richard Murray; Gulsevil Bilgen; Andrew J. Eszterhas


american thoracic society international conference | 2012

Lifetime Management Of COPD Via A Clinical Guidance System – A Long Term Continuous Improvement Model In Its 10th Year

Brian Tiep; Mary Barnett; Rick Carter; Richard Murray


american thoracic society international conference | 2011

Long Term Management Of COPD Via A Clinical Guidance System: Nine Years Of A Continuous Improvement Model

Brian Tiep; Mary Barnett; Rick Carter; Richard Murray


american thoracic society international conference | 2009

Collaborative Management of COPD Via a Clinical Guidance System: A Continuous Improvement Design.

Brian Tiep; Mary Barnett; Richard Murray; Rick Carter

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Brian Tiep

City of Hope National Medical Center

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Gulsevil Bilgen

University of Pennsylvania

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Rick Carter

University of Texas Health Science Center at Tyler

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Ian P. Hall

University of Nottingham

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