[HTML][HTML] Complex interplay between autophagy and oxidative stress in the development of pulmonary disease

W Ornatowski, Q Lu, M Yegambaram, AE Garcia… - Redox biology, 2020 - Elsevier
The autophagic pathway involves the encapsulation of substrates in double-membraned
vesicles, which are subsequently delivered to the lysosome for enzymatic degradation and …

Transglutaminase regulation of cell function

RL Eckert, MT Kaartinen, M Nurminskaya… - Physiological …, 2014 - journals.physiology.org
Transglutaminases (TGs) are multifunctional proteins having enzymatic and scaffolding
functions that participate in regulation of cell fate in a wide range of cellular systems and are …

Defective CFTR induces aggresome formation and lung inflammation in cystic fibrosis through ROS-mediated autophagy inhibition

A Luciani, VR Villella, S Esposito, N Brunetti-Pierri… - Nature cell …, 2010 - nature.com
Accumulation of unwanted/misfolded proteins in aggregates has been observed in airways
of patients with cystic fibrosis (CF), a life-threatening genetic disorder caused by mutations in …

Transglutaminases and disease: lessons from genetically engineered mouse models and inherited disorders

SE Iismaa, BM Mearns, L Lorand… - Physiological …, 2009 - journals.physiology.org
The human transglutaminase (TG) family consists of a structural protein, protein 4.2, that
lacks catalytic activity, and eight zymogens/enzymes, designated factor XIII-A (FXIII-A) and …

Cellular functions of tissue transglutaminase

MV Nurminskaya, AM Belkin - International review of cell and molecular …, 2012 - Elsevier
Transglutaminase 2 (TG2 or tissue transglutaminase) is a highly complex multifunctional
protein that acts as transglutaminase, GTPase/ATPase, protein disulfide isomerase, and …

Systemic analysis of PPARγ in mouse macrophage populations reveals marked diversity in expression with critical roles in resolution of inflammation and airway …

EL Gautier, A Chow, R Spanbroek… - The Journal of …, 2012 - journals.aai.org
Although peroxisome proliferator-activated receptor γ (PPARγ) has anti-inflammatory actions
in macrophages, which macrophage populations express PPARγ in vivo and how it …

Restoration of CFTR function in patients with cystic fibrosis carrying the F508del-CFTR mutation

DD Stefano, VR Villella, S Esposito, A Tosco, A Sepe… - Autophagy, 2014 - Taylor & Francis
Restoration of BECN1/Beclin 1-dependent autophagy and depletion of SQSTM1/p62 by
genetic manipulation or autophagy-stimulatory proteostasis regulators, such as cystamine …

Lysosomal accumulation of gliadin p31–43 peptide induces oxidative stress and tissue transglutaminase-mediated PPARγ downregulation in intestinal epithelial cells …

A Luciani, VR Villella, A Vasaturo, I Giardino… - Gut, 2010 - gut.bmj.com
Background An unresolved question in coeliac disease is to understand how some toxic
gliadin peptides, in particular p31–43, can initiate an innate response and lead to tissue …

The extracellular matrix in bronchopulmonary dysplasia: target and source

I Mižíková, RE Morty - Frontiers in medicine, 2015 - frontiersin.org
Bronchopulmonary dysplasia (BPD) is a common complication of preterm birth that
contributes significantly to morbidity and mortality in neonatal intensive care units. BPD …

Innate and adaptive immunity in cystic fibrosis

EM Bruscia, TL Bonfield - Clinics in chest medicine, 2016 - chestmed.theclinics.com
The airway epithelium works as a physical barrier between the external environment and
internal structures, which represent the lung's first defense against inhaled microorganisms …