scholarly journals 648: KLF5 regulates CFTR gene expression in the human airway epithelium

2021 ◽  
Vol 20 ◽  
pp. S308
Author(s):  
A. Paranjapye ◽  
M. NandyMazumdar ◽  
J. Browne ◽  
S. Leir ◽  
A. Harris
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Nadzeya Marozkina ◽  
Laura Smith ◽  
Yi Zhao ◽  
Joe Zein ◽  
James F. Chmiel ◽  
...  

AbstractEndothelial hemoglobin (Hb)α regulates endothelial nitric oxide synthase (eNOS) biochemistry. We hypothesized that Hb could also be expressed and biochemically active in the ciliated human airway epithelium. Primary human airway epithelial cells, cultured at air–liquid interface (ALI), were obtained by clinical airway brushings or from explanted lungs. Human airway Hb mRNA data were from publically available databases; or from RT-PCR. Hb proteins were identified by immunoprecipitation, immunoblot, immunohistochemistry, immunofluorescence and liquid chromatography- mass spectrometry. Viral vectors were used to alter Hbβ expression. Heme and nitrogen oxides were measured colorimetrically. Hb mRNA was expressed in human ciliated epithelial cells. Heme proteins (Hbα, β, and δ) were detected in ALI cultures by several methods. Higher levels of airway epithelial Hbβ gene expression were associated with lower FEV1 in asthma. Both Hbβ knockdown and overexpression affected cell morphology. Hbβ and eNOS were apically colocalized. Binding heme with CO decreased extracellular accumulation of nitrogen oxides. Human airway epithelial cells express Hb. Higher levels of Hbβ gene expression were associated with airflow obstruction. Hbβ and eNOS were colocalized in ciliated cells, and heme affected oxidation of the NOS product. Epithelial Hb expression may be relevant to human airways diseases.


1993 ◽  
Vol 75 (3) ◽  
pp. 1256-1262 ◽  
Author(s):  
S. C. Erzurum ◽  
C. Danel ◽  
A. Gillissen ◽  
C. S. Chu ◽  
B. C. Trapnell ◽  
...  

Human bronchial epithelium is exquisitely sensitive to high O2 levels, with tracheobronchitis usually developing after 12 h of exposure to 100% O2. To evaluate whether this vulnerability results from inability of the bronchial epithelium to provide adequate antioxidant protection, we quantified antioxidant gene expression in bronchial epithelium of normal volunteers at baseline and after exposure to 100% O2 in vivo. After 14.8 +/- 0.2 h of 100% O2, 24 of 33 individuals had evidence of tracheobronchitis. Baseline gene expression of CuZn superoxide dismutase (SOD), MnSOD, and catalase in bronchial epithelium was very low (CuZnSOD 4.1 +/- 0.8 transcripts/cell, MnSOD 5.1 +/- 0.9, catalase 1.3 +/- 0.2), with control gamma-actin expression relatively abundant (50 +/- 6 transcripts/cell). Importantly, despite 100% O2 exposure sufficient to cause tracheobronchitis in most individuals, antioxidant mRNA transcripts/cell in bronchial epithelium did not increase (P > 0.5). Catalase activity in bronchial epithelium did not change after exposure to hyperoxia (P > 0.05). Total SOD activity increased mildly (P < 0.01) but not sufficiently to protect the epithelium. Together, the very low levels of expression of intracellular antioxidant enzymes and the inability to upregulate expression at the mRNA level with oxidant stress likely have a role in human airway epithelium susceptibility to hyperoxia.


BMC Genomics ◽  
2009 ◽  
Vol 10 (1) ◽  
pp. 493 ◽  
Author(s):  
Tina Raman ◽  
Timothy P O'Connor ◽  
Neil R Hackett ◽  
Wei Wang ◽  
Ben-Gary Harvey ◽  
...  

2009 ◽  
Vol 106 (7) ◽  
pp. 2319-2324 ◽  
Author(s):  
F. Schembri ◽  
S. Sridhar ◽  
C. Perdomo ◽  
A. M. Gustafson ◽  
X. Zhang ◽  
...  

2006 ◽  
Vol 35 (4) ◽  
pp. 424-435 ◽  
Author(s):  
Arnaud Chambellan ◽  
Paul J. Cruickshank ◽  
Patrick McKenzie ◽  
Steven B. Cannady ◽  
Katalin Szabo ◽  
...  

2006 ◽  
Vol 453 (6) ◽  
pp. 777-785 ◽  
Author(s):  
Peter Steen Pedersen ◽  
Thomas Hartig Braunstein ◽  
Anders Jørgensen ◽  
Per Leganger Larsen ◽  
Niels-Henrik Holstein-Rathlou ◽  
...  

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