Scientists at Children's Hospital Los Angeles Identify Mechanism Critical to Lung Formation and Regeneration

Eya1 phosphatase acts to maintain barrier integrity in the lung

LOS ANGELES--(BUSINESS WIRE)--Jul 2, 2012 - Scientists have provided the first evidence that an enzyme called Eya1 protein phosphatase is a critical regulator of lung function and that this may have broad implications for sufferers of a variety of pulmonary diseases. “Identification of the role of Eya1 in establishing pulmonary tight junction and barrier integrity could have a significant impact on asthma, chronic obstructive pulmonary disease, and acute respiratory distress syndrome, all diseases characterized with disruptions in permeability,” said Ahmed El-Hashash, PhD, investigator at The Saban Research Institute of Children's Hospital Los Angeles and assistant professor at the Keck School of Medicine.

 

Ahmed El-Hashash, PhD, and David Warburton, MD, of The Saban Research Institute (Photo: Business Wir ... Ahmed El-Hashash, PhD, and David Warburton, MD, of The Saban Research Institute (Photo: Business Wire)

 

Proper formation of lung epithelium is essential to life. The normal growth and functioning of the lung depends on the formation of tight junctions between adjacent cells making up the alveolar epithelial sheet, a thin layer of tissue separating neighboring alveoli. Alveoli are the site of gas exchange between the lung and blood vessels. Loss of these tight junctions alters the exchange of oxygen and carbon dioxide. Permeability dysfunction has been implicated in both acute lung injury and acute respiratory distress syndrome, a life-threatening lung condition that prevents adequate oxygen from getting from the lungs and into the blood.

Until now, very little has been known about the basic regulatory mechanisms underlying permeability barrier formation and integrity of the lung epithelium. David Warburton, MD, director of Developmental Biology and Regenerative Medicine at The Saban Research Institute, and El-Hashash provided the first evidence that the enzyme Eya1 protein phosphatase controls tight junction and permeability barrier formation in the lung epithelium. They have also provided the first evidence that Eya1 enzyme coordinates a complex network of other cellular proteins and molecules that are essential for epithelial barrier integrity, and are therefore critical to optimal lung function. Both in vivo and in vitro experiments showed that interfering with Eya1 phosphatase function resulted in defective formation of tight junctions and the permeability barrier.

“These findings identify a novel therapeutic option for lung diseases like COPD and ARDS,” said Warburton. “Our discovery of Eya1 enzyme control of pulmonary barrier integrity suggests that influencing alveolar epithelial junction formation by manipulating the activity of enzymes has the potential to identify future targets for the treatment of lung injury and may provide solutions to the problems concerning regeneration of lung tissue for restoration of functional alveoli.”

Results of the study will be published in the Journal of Cell Science.

About Children's Hospital Los Angeles

Children's Hospital Los Angeles has been named the best children's hospital in California and among the top five in the nation for clinical excellence with its selection to the prestigious US News & World Report Honor Roll. Children's Hospital is home to The Saban Research Institute, one of the largest and most productive pediatric research facilities in the United States, is one of America's premier teaching hospitals and has been affiliated with the Keck School of Medicine of the University of Southern California since 1932.

For more information, visit www.CHLA.org. Follow us on Twitter, Facebook, YouTube and LinkedIn, or visit our blog: www.WeAreCHLA.org.

Photos/Multimedia Gallery Available: http://www.businesswire.com/cgi-bin/mmg.cgi?eid=50330043&lang=en

 

 

Contact: Children's Hospital Los Angeles
Ellin Kavanagh, 323-361-8505
ekavanagh@chla.usc.edu

 

 

Posted: July 2012

View comments

Hide
(web2)