Literature DB >> 17071725

Aberrant cytoplasmic sequestration of eNOS in endothelial cells after monocrotaline, hypoxia, and senescence: live-cell caveolar and cytoplasmic NO imaging.

Somshuvra Mukhopadhyay1, Fang Xu, Pravin B Sehgal.   

Abstract

We previously reported the disruption of caveolae/rafts, dysfunction of Golgi tethers, N-ethylmaleimide-sensitive factor-attachment protein (SNAP) receptor proteins (SNAREs), and SNAPs, and inhibition of anterograde trafficking in endothelial cells in culture and rat lung exposed to monocrotaline pyrrole (MCTP) as a prelude to the development of pulmonary hypertension. We have now investigated 1) whether this trafficking block affects subcellular localization and function of endothelial nitric oxide (NO) synthase (eNOS) and 2) whether Golgi blockade and eNOS sequestration are observed after hypoxia and senescence. Immunofluorescence data revealed that MCTP-induced "megalocytosis" of pulmonary arterial endothelial cells (PAEC) was accompanied by a loss of eNOS from the plasma membrane, with increased accumulation in the cytoplasm. This cytoplasmic eNOS was sequestered in heterogeneous compartments and partially colocalized with Golgi and endoplasmic reticulum (ER) markers, caveolin-1, NOSTRIN, and ER Tracker, but not Lyso Tracker. Hypoxia and senescence also produced enlarged PAEC, with dysfunctional Golgi and loss of eNOS from the plasma membrane, with sequestration in the cytoplasm. Live-cell imaging of caveolar and cytoplasmic NO with 4,5-diaminofluorescein diacetate (DAF-2DA) as probe showed a marked loss of caveolar NO after MCTP, hypoxia, and senescence. Although ionomycin stimulated DAF-2DA fluorescence in control PAEC, this ionophore decreased DAF-2DA fluorescence in MCTP-treated and senescent PAEC, suggesting localization of eNOS in an aberrant cytoplasmic compartment that was readily discharged by Ca(2+)-induced exocytosis. Thus monocrotaline, hypoxia, and senescence produce a Golgi blockade in PAEC, leading to sequestration of eNOS away from its functional caveolar location and providing a mechanism for the often-reported reduction in pulmonary arterial NO levels in experimental pulmonary hypertension, despite sustained eNOS protein levels.

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Year:  2006        PMID: 17071725     DOI: 10.1152/ajpheart.00990.2006

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  25 in total

1.  Abnormal expression of NSF, α-SNAP and SNAP23 in pulmonary arterial hypertension in rats treated with monocrotaline.

Authors:  Hong-Liang Zhang; Zhi-Hong Liu; Qin Luo; Yong Wang; Zhi-Hui Zhao
Journal:  Int J Clin Exp Med       Date:  2015-02-15

Review 2.  Specificity in S-nitrosylation: a short-range mechanism for NO signaling?

Authors:  Antonio Martínez-Ruiz; Inês M Araújo; Alicia Izquierdo-Álvarez; Pablo Hernansanz-Agustín; Santiago Lamas; Juan M Serrador
Journal:  Antioxid Redox Signal       Date:  2013-01-04       Impact factor: 8.401

3.  The xanthine derivative KMUP-1 inhibits models of pulmonary artery hypertension via increased NO and cGMP-dependent inhibition of RhoA/Rho kinase.

Authors:  Hui-Hsuan Chung; Zen-Kong Dai; Bin-Nan Wu; Jwu-Lai Yeh; Chee-Yin Chai; Koung-Shing Chu; Chung-Pin Liu; Ing-Jun Chen
Journal:  Br J Pharmacol       Date:  2010-06       Impact factor: 8.739

4.  Autophagic protein LC3B confers resistance against hypoxia-induced pulmonary hypertension.

Authors:  Seon-Jin Lee; Akaya Smith; Lanping Guo; Tero-Pekka Alastalo; Molong Li; Hirofumi Sawada; Xiaoli Liu; Zhi-Hua Chen; Emeka Ifedigbo; Yang Jin; Carol Feghali-Bostwick; Stefan W Ryter; Hong Pyo Kim; Marlene Rabinovitch; Augustine M K Choi
Journal:  Am J Respir Crit Care Med       Date:  2010-10-01       Impact factor: 21.405

Review 5.  Endothelial nitric oxide (NO) and its pathophysiologic regulation.

Authors:  Anuran Chatterjee; Stephen M Black; John D Catravas
Journal:  Vascul Pharmacol       Date:  2008-07-20       Impact factor: 5.773

6.  Nitric oxide scavenging causes remodeling of the endoplasmic reticulum, Golgi apparatus and mitochondria in pulmonary arterial endothelial cells.

Authors:  Jason E Lee; Huijuan Yuan; Feng-Xia Liang; Pravin B Sehgal
Journal:  Nitric Oxide       Date:  2013-06-14       Impact factor: 4.427

Review 7.  Life history of eNOS: partners and pathways.

Authors:  David M Dudzinski; Thomas Michel
Journal:  Cardiovasc Res       Date:  2007-04-03       Impact factor: 10.787

8.  Golgi dysfunction is a common feature in idiopathic human pulmonary hypertension and vascular lesions in SHIV-nef-infected macaques.

Authors:  Pravin B Sehgal; Somshuvra Mukhopadhyay; Kirit Patel; Fang Xu; Sharilyn Almodóvar; Rubin M Tuder; Sonia C Flores
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2009-07-31       Impact factor: 5.464

9.  Golgi, trafficking, and mitosis dysfunctions in pulmonary arterial endothelial cells exposed to monocrotaline pyrrole and NO scavenging.

Authors:  Jason Lee; Reuben Reich; Fang Xu; Pravin B Sehgal
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2009-07-31       Impact factor: 5.464

10.  Caveolin-1 Expression and Hemodynamics in COPD Patients.

Authors:  Lars C Huber; Alex Soltermann; Manuel Fischler; Steffen Gay; Walter Weder; Erich W Russi; Rudolf Speich; Silvia Ulrich
Journal:  Open Respir Med J       Date:  2009-05-13
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