Literature DB >> 34716469

Evaluation of Cardiotonic Steroid Modulation of Cellular Cholesterol and Phospholipid.

Lilian N D Silva1,2, Israel J P Garcia1,2, Jessica M M Valadares1,2, Marco Tulio C Pessoa1,2, Marina Marques Toledo1,2, Matheus V Machado3, Mileane Souza Busch4, Isabella Rocha4, José Augusto F P Villar3, Georgia C Atella4, Herica L Santos1,2, Vanessa F Cortes5,6, Leandro A Barbosa7,8.   

Abstract

We have previously shown that 21-benzylidene digoxin (21-BD) increases the total cholesterol and phospholipid content on the membrane of HeLa cells. Lipid modulation caused by cardiotonic steroids (CTS) is still unexplored. Therefore, the aim of the present study was to evaluate the cholesterol and phospholipid modulation of the cell membrane caused by ouabain and 21-BD and the possible involvement of the caveolae on this modulation. For this, one cell line containing caveolae (HeLa) and other not containing (Caco-2) were used. The modulation of the lipid profile was evaluated by total cholesterol and phospholipids measurements, and identification of membrane phospholipids by HPTLC. The cholesterol distribution was evaluated by filipin staining. The caveolin-1 expression was evaluated by Western Blotting. Ouabain had no effect on the total membrane lipid content in both cell lines. However, 21-BD increased total membrane phospholipid content and had no effect on the membrane cholesterol content in Caco-2 cells. CTS were not able to alter the specific phospholipids content. In the filipin experiments, 21-BD provoked a remarkable redistribution of cholesterol to the perinuclear region of HeLa cells. In Caco-2 cells, it was observed only a slight increase in cholesterol, especially as intracellular vesicles. The caveolin-1 expression was not altered by any of the compounds. Our data mainly show different effects of two cardiotonic steroids. Ouabain had no effect on the lipid profile of cells, whereas 21-BD causes important changes in cholesterol and phospholipid content. Therefore, the modulation of cholesterol content in the plasma membrane of HeLa cells is not correlated with the expression of caveolin-1.
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Cardiotonic steroids; Caveolae; Lipid modulation; Na,K-ATPase

Mesh:

Substances:

Year:  2021        PMID: 34716469     DOI: 10.1007/s00232-021-00203-z

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  61 in total

Review 1.  Sodium/potassium ATPase (Na+, K+-ATPase) and ouabain/related cardiac glycosides: A new paradigm for development of anti- breast cancer drugs?

Authors:  Jin-Qiang Chen; Ruben G Contreras; Richard Wang; Sandra V Fernandez; Liora Shoshani; Irma H Russo; Marcelino Cereijido; Jose Russo
Journal:  Breast Cancer Res Treat       Date:  2005-12-02       Impact factor: 4.872

2.  Regulation of intracellular cholesterol distribution by Na/K-ATPase.

Authors:  Yiliang Chen; Ting Cai; Haojie Wang; Zhichuan Li; Elizabeth Loreaux; Jerry B Lingrel; Zijian Xie
Journal:  J Biol Chem       Date:  2009-04-10       Impact factor: 5.157

3.  The scaffolding domain of caveolin 2 is responsible for its Golgi localization in Caco-2 cells.

Authors:  Lionel Breuza; Séverine Corby; Jean-Pierre Arsanto; Marie-Hélène Delgrossi; Peter Scheiffele; André Le Bivic
Journal:  J Cell Sci       Date:  2002-12-01       Impact factor: 5.285

4.  Role of cholesterol in developing T-tubules: analogous mechanisms for T-tubule and caveolae biogenesis.

Authors:  A J Carozzi; E Ikonen; M R Lindsay; R G Parton
Journal:  Traffic       Date:  2000-04       Impact factor: 6.215

5.  Modulation of Na,K-ATPase and Na-ATPase activity by phospholipids and cholesterol. I. Steady-state kinetics.

Authors:  F Cornelius
Journal:  Biochemistry       Date:  2001-07-31       Impact factor: 3.162

6.  Regulation of alpha1 Na/K-ATPase expression by cholesterol.

Authors:  Yiliang Chen; Xin Li; Qiqi Ye; Jiang Tian; Runming Jing; Zijian Xie
Journal:  J Biol Chem       Date:  2011-03-01       Impact factor: 5.157

7.  Digoxin and ouabain induce the efflux of cholesterol via liver X receptor signalling and the synthesis of ATP in cardiomyocytes.

Authors:  Ivana Campia; Valentina Sala; Joanna Kopecka; Christian Leo; Nico Mitro; Costanzo Costamagna; Donatella Caruso; Gianpiero Pescarmona; Tiziana Crepaldi; Dario Ghigo; Amalia Bosia; Chiara Riganti
Journal:  Biochem J       Date:  2012-10-15       Impact factor: 3.857

8.  Digoxin and ouabain increase the synthesis of cholesterol in human liver cells.

Authors:  I Campia; E Gazzano; G Pescarmona; D Ghigo; A Bosia; C Riganti
Journal:  Cell Mol Life Sci       Date:  2009-05       Impact factor: 9.261

9.  Modulation of Na,K-ATPase by phospholipids and cholesterol. II. Steady-state and presteady-state kinetics.

Authors:  Flemming Cornelius; Nigel Turner; Hanne R Z Christensen
Journal:  Biochemistry       Date:  2003-07-22       Impact factor: 3.162

10.  Regulation of caveolin-1 membrane trafficking by the Na/K-ATPase.

Authors:  Ting Cai; Haojie Wang; Yiliang Chen; Lijun Liu; William T Gunning; Luis Eduardo M Quintas; Zi-Jian Xie
Journal:  J Cell Biol       Date:  2008-09-15       Impact factor: 10.539

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  1 in total

1.  Digoxin Derivatives Sensitize a Saccharomyces cerevisiae Mutant Strain to Fluconazole by Inhibiting Pdr5p.

Authors:  Daniel Clemente de Moraes; Ana Claudia Tessis; Rodrigo Rollin-Pinheiro; Jefferson Luiz Princival; José Augusto Ferreira Perez Villar; Leandro Augusto Barbosa; Eliana Barreto-Bergter; Antônio Ferreira-Pereira
Journal:  J Fungi (Basel)       Date:  2022-07-25
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