Literature DB >> 19954818

Abnormal expression of telomerase/apoptosis limits type II alveolar epithelial cell replication in the early remodeling of usual interstitial pneumonia/idiopathic pulmonary fibrosis.

Daniel Reis Waisberg1, João Valente Barbas-Filho, Edwin Roger Parra, Sandra Fernezlian, Carlos Roberto Ribeiro de Carvalho, Ronaldo Adib Kairalla, Vera Luiza Capelozzi.   

Abstract

Idiopathic pulmonary fibrosis is a distinctive, usually fatal, type of chronic fibrosing interstitial pneumonia of unknown cause that increases in prevalence with advanced age, characterized by failure of alveolar re-epithelization and progressive scar formation. Recently, limitation of the replicative capacity of tissues determined by telomerase/apoptosis balance has been implicated in pathogenesis of age-related diseases. In this study, we validated the importance of the expression of type 2 alveolar epithelial cells telomerase protein and studied the relationships between telomerase and apoptosis in early remodeling of usual interstitial pneumonia. We determined type 2 alveolar epithelial cells density, telomerase expression, and apoptosis in surgical lung biopsies from 24 patients with usual interstitial pneumonia, and in normal lung tissues from 18 subjects. We used immunohistochemistry, deoxynucleotidyl transferase method of end labeling, electron microscopy, and histomorphometry to evaluate the amount of type 2 alveolar epithelial cells staining for surfactant-A, telomerase, and in situ detection of apoptotic cells. Unaffected areas of usual interstitial pneumonia and normal lung tissue had similar densities of type 2 alveolar epithelial cells, but a significant minor subpopulation of type 2 alveolar epithelial cells was telomerase positive and a large population was telomerase negative. A significant inverse association was found between low type 2 alveolar epithelial cell telomerase expression and high apoptosis in unaffected areas of usual interstitial pneumonia. Although type 2 alveolar epithelial cell telomerase expression was higher than apoptosis in NLT group, no significant association was found between them. Electron microscopy confirmed epithelial apoptosis, alveolar collapse, and initial fibroplasia. We conclude that abnormal type 2 alveolar epithelial cells telomerase/apoptosis balance may reduce alveolar epithelial regenerative capacity, thus contributing to the early remodeling response in usual interstitial pneumonia. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2009        PMID: 19954818     DOI: 10.1016/j.humpath.2009.08.019

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  16 in total

Review 1.  Idiopathic pulmonary fibrosis-an epidemiological and pathological review.

Authors:  Andrea T Borchers; Christopher Chang; Carl L Keen; M Eric Gershwin
Journal:  Clin Rev Allergy Immunol       Date:  2011-04       Impact factor: 8.667

Review 2.  The Role of Aging in Idiopathic Pulmonary Fibrosis.

Authors:  Joseph Leung; Young Cho; Richard F Lockey; Narasaiah Kolliputi
Journal:  Lung       Date:  2015-04-23       Impact factor: 2.584

Review 3.  Is Progression of Pulmonary Fibrosis due to Ventilation-induced Lung Injury?

Authors:  Richard K Albert; Bradford Smith; Carrie E Perlman; David A Schwartz
Journal:  Am J Respir Crit Care Med       Date:  2019-07-15       Impact factor: 21.405

4.  Telomerase Deficiency Causes Alveolar Stem Cell Senescence-associated Low-grade Inflammation in Lungs.

Authors:  Ruping Chen; Kexiong Zhang; Hao Chen; Xiaoyin Zhao; Jianqiu Wang; Li Li; Yusheng Cong; Zhenyu Ju; Dakang Xu; Bryan R G Williams; Jihui Jia; Jun-Ping Liu
Journal:  J Biol Chem       Date:  2015-10-30       Impact factor: 5.157

Review 5.  Stem Cell-Based Therapy in Idiopathic Pulmonary Fibrosis.

Authors:  Marek Barczyk; Matthias Schmidt; Sabrina Mattoli
Journal:  Stem Cell Rev Rep       Date:  2015-08       Impact factor: 5.739

6.  Cellular senescence and senescence-associated secretory phenotype: comparison of idiopathic pulmonary fibrosis, connective tissue disease-associated interstitial lung disease, and chronic obstructive pulmonary disease.

Authors:  Ryo Okuda; Kazutetsu Aoshiba; Hidekazu Matsushima; Takashi Ogura; Koji Okudela; Kenichi Ohashi
Journal:  J Thorac Dis       Date:  2019-03       Impact factor: 2.895

7.  Increased fibroblast telomerase expression precedes myofibroblast α-smooth muscle actin expression in idiopathic pulmonary fibrosis.

Authors:  Daniel Reis Waisberg; Edwin Roger Parra; João Valente Barbas-Filho; Sandra Fernezlian; Vera Luiza Capelozzi
Journal:  Clinics (Sao Paulo)       Date:  2012-09       Impact factor: 2.365

8.  Vascular dysfunction by myofibroblast activation in patients with idiopathic pulmonary fibrosis and prognostic significance.

Authors:  E R Parra; R Falzoni; V L Capelozzi
Journal:  Braz J Med Biol Res       Date:  2012-04-26       Impact factor: 2.590

Review 9.  Lung epithelial stem cells and their niches: Fgf10 takes center stage.

Authors:  Thomas Volckaert; Stijn De Langhe
Journal:  Fibrogenesis Tissue Repair       Date:  2014-05-08

10.  Modeling pulmonary fibrosis by abnormal expression of telomerase/apoptosis/collagen V in experimental usual interstitial pneumonia.

Authors:  E R Parra; M S Pincelli; W R Teodoro; A P P Velosa; V Martins; M P Rangel; J V Barbas-Filho; V L Capelozzi
Journal:  Braz J Med Biol Res       Date:  2014-06-04       Impact factor: 2.590

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