Literature DB >> 28925080

Specific knock-down of tissue non-specific alkaline phosphatase mRNA levels inhibits intracellular lipid accumulation in 3T3-L1 and HepG2 cells.

George Chirambo1,2, Chantal van Niekerk1, Nigel J Crowther1.   

Abstract

The use of non-specific inhibitors of tissue non-specific alkaline phosphatase (TNSALP) in pre-adipocytes blocks intracellular lipid accumulation. TNSALP is also expressed in hepatocytes, which are known to accumulate lipid in a similar manner to pre-adipocytes. The purpose of this study was to use specific silencing of TNSALP mRNA, using short interfering (si) RNA, to investigate the role of TNSALP in intracellular lipid accumulation in 3T3-L1 and HepG2 cells. Cellular activity of TNSALP was measured using an automated colorimetric assay, and intracellular lipid accumulation was determined using the lipid-specific dye, Oil Red O. Cells were transfected with siRNA directed against TNSALP mRNA, and expression of the TNSALP gene was determined at selected time points postinduction of lipid droplet formation. Expression of the TNSALP gene was inhibited by a maximum of 88 ± 1.9% (P < 0.005 vs. control) 11 days after initiation of lipid droplet formation in the 3T3-L1 cells and 80 ± 8.9% (P < 0.05 vs. control) after 4 days in the HepG2 cells. This led to significant inhibition of both TNSALP activity and intracellular lipid accumulation in both cell lines. These data demonstrates that TNSALP plays an important role in the control of lipid droplet formation in both pre-adipocyte and hepatocyte cell lines.
© 2017 The Authors. International Journal of Experimental Pathology © 2017 International Journal of Experimental Pathology.

Entities:  

Keywords:  3T3-L1 cells; HepG2 cells; adipogenesis; alkaline phosphatase; lipid droplets; siRNA

Mesh:

Substances:

Year:  2017        PMID: 28925080      PMCID: PMC5743820          DOI: 10.1111/iep.12243

Source DB:  PubMed          Journal:  Int J Exp Pathol        ISSN: 0959-9673            Impact factor:   1.925


  46 in total

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Journal:  Anal Biochem       Date:  2006-05-11       Impact factor: 3.365

2.  Comparing two small samples with an unstable, treatment-independent baseline.

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Journal:  J Dairy Sci       Date:  1989-10       Impact factor: 4.034

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Authors:  H Van Belle
Journal:  Clin Chem       Date:  1976-07       Impact factor: 8.327

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Authors:  Claudia Hernández-Mosqueira; Cristina Velez-delValle; Walid Kuri-Harcuch
Journal:  Biochim Biophys Acta       Date:  2015-09-21

6.  Alkaline phosphatase retained in HepG2 hepatocarcinoma cells vs. alkaline phosphatase released to culture medium: difference of aberrant glycosylation.

Authors:  Azin Nowrouzi; Razieh Yazdanparast
Journal:  Biochem Biophys Res Commun       Date:  2005-05-06       Impact factor: 3.575

Review 7.  Peroxisome proliferator-activated receptor-gamma: from adipogenesis to carcinogenesis.

Authors:  L Fajas; M B Debril; J Auwerx
Journal:  J Mol Endocrinol       Date:  2001-08       Impact factor: 5.098

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Journal:  Ann Clin Biochem       Date:  1993-07       Impact factor: 2.057

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Authors:  S Narisawa; N Fröhlander; J L Millán
Journal:  Dev Dyn       Date:  1997-03       Impact factor: 3.780

10.  Immunolocalization of alkaline phosphatase and surfactant-like particle proteins in rat duodenum during fat absorption.

Authors:  Y Zhang; J S Shao; Q M Xie; D H Alpers
Journal:  Gastroenterology       Date:  1996-02       Impact factor: 22.682

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  1 in total

1.  2-Benzylidenebenzofuran-3(2H)-ones as a new class of alkaline phosphatase inhibitors: synthesis, SAR analysis, enzyme inhibitory kinetics and computational studies.

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Journal:  RSC Adv       Date:  2021-10-29       Impact factor: 4.036

  1 in total

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